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Isoflavonoids of the Leguminosae

https://doi.org/10.1039/b511238a
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Detection of isoflavonoids and their glycosides by liquid chromatography/electrospray ionization mass spectrometry in root extracts of lupin (Lupinus albus)
inferredcites →https://doi.org/10.1002/1522-2675(200203)85:3<847::aid-hlca847>3.0.co;2-6openalex-snapshot
New Pterocarpanoids of Crotalaria pallida and Crotalaria assamica
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An enantiomeric assay for the flavonoids medicarpin and vestitone using capillary electrophoresis
inferredcites →https://doi.org/10.1002/1522-2683(200206)23:11<1642::aid-elps1642>3.0.co;2-yopenalex-snapshot
Profiling isoflavonoids found in legume root extracts using capillary electrophoresis
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Six New Constituents from the Roots of Erythrina variegata
inferredcites →https://doi.org/10.1002/cbdv.200590000openalex-snapshot
Strategies and Tools for Structure Determination of Natural Products Using Modern Methods of NMR Spectroscopy
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Ueber Iridin, das Glucosid der Veilchenwurzel
inferredcites →https://doi.org/10.1002/chir.10235openalex-snapshot
Chiroptical properties and synthesis of enantiopure cis and trans Pterocarpan Skeleton
inferredcites →https://doi.org/10.1002/cjoc.200890100openalex-snapshot
Three New Prenylfuranoisoflavonoids from the Roots of Hedysarum scoparium
inferredcites →https://doi.org/10.1002/ejoc.200600742openalex-snapshot
Uncommon 5‐Methoxyisoflavans from Desmodium canum
inferredcites →https://doi.org/10.1002/hlca.200890108openalex-snapshot
Three New Isoflavonoids from the Aerial Parts of Ammopiptanthus mongolicus
inferredcites →https://doi.org/10.1002/jccs.200200066openalex-snapshot
The Constituents of Euchresta Formosana
inferredcites →https://doi.org/10.1002/jccs.200400210openalex-snapshot
Flavonoids from the Flowers of Pueraria Lobata
inferredcites →https://doi.org/10.1002/jlac.197419740816openalex-snapshot
Natürlich vorkommende Chinone, XXIV1) Über die Inhaltsstoffe von Bowdichia nitida Benth.: Erstmalige Isolierung eines Isoflavonchinons
inferredcites →https://doi.org/10.1002/jms.1344openalex-snapshot
Evaluation of glycosylation and malonylation patterns in flavonoid glycosides during LC/MS/MS metabolite profiling
inferredcites →https://doi.org/10.1002/jms.884openalex-snapshot
Profiling isoflavone conjugates in root extracts of lupine species with LC/ESI/MSn systems
inferredcites →https://doi.org/10.1002/jps.2600531213openalex-snapshot
Isolation of Coumestrol and Other Phenolics from Alfalfa by Countercurrent Distribution
inferredcites →https://doi.org/10.1002/jssc.200401844openalex-snapshot
Liquid chromatography coupled to nuclear magnetic resonance spectroscopy for the identification of isoflavone glucoside malonates in T. pratense L. leaves.
inferredcites →https://doi.org/10.1002/jssc.200700569openalex-snapshot
Current trends in isolation, separation, determination and identification of isoflavones: A review
inferredcites →https://doi.org/10.1002/mrc.1632openalex-snapshot
LC–NMR coupling technology: recent advancements and applications in natural products analysis
inferredcites →https://doi.org/10.1002/mrc.1806openalex-snapshot
Solvent effect in 1H NMR spectra of 3′‐hydroxy‐4′‐methoxy isoflavonoids from Astragalus membranaceus var. mongholicus
inferredcites →https://doi.org/10.1002/mrc.2138openalex-snapshot
NMR spectral assignments of a new [COC] isoflavone dimer from Andira surinamensis
inferredcites →https://doi.org/10.1002/mrc.2269openalex-snapshot
Complete NMR data assignments for novel pterocarpans from Harpalyce brasiliana
inferredcites →https://doi.org/10.1002/mrc.2336openalex-snapshot
Prenylated isoflavones from Flemingia philippinensis
inferredcites →https://doi.org/10.1002/pca.1073openalex-snapshot
Differentiation of isomeric malonylated flavonoid glyconjugates in plant extracts with UPLC‐ESI/MS/MS
inferredcites →https://doi.org/10.1002/pca.603openalex-snapshot
Characterisation of soy isoflavones and screening for novel malonyl glycosides using high‐performance liquid chromatography–electrospray ionisation–mass spectrometry
inferredcites →https://doi.org/10.1002/pca.946openalex-snapshot
On‐line identification of phenolic compounds of Trifolium species using HPLC‐UV‐MS and post‐column UV‐derivatisation
inferredcites →https://doi.org/10.1002/pca.951openalex-snapshot
Identification of isoflavone glycosides in Pueraria lobata cultures by tandem mass spectrometry
inferredcites →https://doi.org/10.1002/prac.18550650147openalex-snapshot
Ueber die Wurzel der Ononis spinosa
inferredcites →https://doi.org/10.1002/ptr.1556openalex-snapshot
Antibacterial activity of phytochemicals isolated from Erythrina zeyheri against vancomycin‐resistant enterococci and their combinations with vancomycin
inferredcites →https://doi.org/10.1002/rcm.1936openalex-snapshot
Liquid chromatography/electrospray ionization mass spectrometry for the characterization of twenty‐three flavonoids in the extract of Dalbergia odorifera
inferredcites →https://doi.org/10.1002/rcm.3277openalex-snapshot
Characterization of phenolic compounds in the crude extract of Hedysarum multijugum by high‐performance liquid chromatography with electrospray ionization tandem mass spectrometry
inferredcites →https://doi.org/10.1006/abbi.1996.0539openalex-snapshot
Affinity Chromatography, Substrate/Product Specificity, and Amino Acid Sequence Analysis of an IsoflavoneO-Methyltransferase from Alfalfa (Medicago sativaL.)
inferredcites →https://doi.org/10.1006/abbi.1999.1238openalex-snapshot
Molecular Characterization of the Enzyme Catalyzing the Aryl Migration Reaction of Isoflavonoid Biosynthesis in Soybean
inferredcites →https://doi.org/10.1006/bbrc.1998.9414openalex-snapshot
CYP81E1, a Cytochrome P450 cDNA of Licorice (Glycyrrhiza echinataL.), Encodes Isoflavone 2′-Hydroxylase
inferredcites →https://doi.org/10.1006/jmre.1996.1056openalex-snapshot
Applying Excitation Sculpting to Construct Singly and Doubly Selective 1D NMR Experiments
inferredcites →https://doi.org/10.1007/bf00910057openalex-snapshot
�ber Inhaltstoffe der Iris germanica (Schwertlilie)
inferredcites →https://doi.org/10.1007/bf02994750openalex-snapshot
A new pterocarpan, (-)-maackiain sulfate, from the roots ofSophora subprostrata
inferredcites →https://doi.org/10.1007/pl00013958openalex-snapshot
Flavonoids of Leguminous Plants: Structure, Biological Activity, and Biosynthesis
inferredcites →https://doi.org/10.1007/s00049-008-0402-7openalex-snapshot
Biologically active secondary metabolites in white clover (Trifolium repens L.) – a review focusing on contents in the plant, plant–pest interactions and transformation
inferredcites →https://doi.org/10.1007/s00216-003-2310-6openalex-snapshot
Flavonoids in Leguminosae: Analysis of extracts of T. pratense L., T. dubium L., T. repens L., and L. corniculatus L. leaves using liquid chromatography with UV, mass spectrometric and fluorescence detection
inferredcites →https://doi.org/10.1007/s00299-005-0972-6openalex-snapshot
Peroxidases have more functions than a Swiss army knife
inferredcites →https://doi.org/10.1007/s00425-003-1118-0openalex-snapshot
cDNA cloning and expression of isoflavonoid-specific glucosyltransferase from Glycyrrhiza echinata cell-suspension cultures
inferredcites →https://doi.org/10.1007/s00425-006-0233-0openalex-snapshot
Engineering isoflavone metabolism with an artificial bifunctional enzyme
inferredcites →https://doi.org/10.1007/s10600-008-0007-yopenalex-snapshot
Two new isoflavonoid monogalactosides from Trifolium pratense roots
inferredcites →https://doi.org/10.1007/s10600-008-9008-0openalex-snapshot
New genistein monogalactoside from the aerial part of Trifolium pratense
inferredcites →https://doi.org/10.1007/s10616-006-9040-5openalex-snapshot
Effect of new rotenoid glycoside from the fruits of Amorpha fruticosa LINNE on the growth of human immune cells
inferredcites →https://doi.org/10.1007/s11094-007-0084-4openalex-snapshot
Phenolic compounds of the genera Glycyrrhiza L. and Meristotropis Fisch. et Mey. (review)
inferredcites →https://doi.org/10.1007/s11101-007-9059-zopenalex-snapshot
Pterocarpans: interesting natural products with antifungal activity and other biological properties
inferredcites →https://doi.org/10.1007/s11103-006-9050-xopenalex-snapshot
Functional analysis of members of the isoflavone and isoflavanone O-methyltransferase enzyme families from the model legume Medicago truncatula
inferredcites →https://doi.org/10.1007/s11103-007-9167-6openalex-snapshot
A functional genomics approach to (iso)flavonoid glycosylation in the model legume Medicago truncatula
inferredcites →https://doi.org/10.1007/s11418-008-0297-1openalex-snapshot
A new arylbenzofuran from the aerial parts of alfalfa
inferredcites →https://doi.org/10.1016/0031-9422(79)83013-7openalex-snapshot
Biosynthesis of the 2-arylbenzofuran phytoalexin vignafuran in Vigna unguiculata
inferredcites →https://doi.org/10.1016/0031-9422(80)85077-1openalex-snapshot
Two prenylflavanones from Euchresta japonica
inferredcites →https://doi.org/10.1016/0031-9422(80)85140-5openalex-snapshot
New prenylated isoflavones and a prenylated dihydroflavonol from Millettia pachycarpa
inferredcites →https://doi.org/10.1016/0031-9422(81)85109-6openalex-snapshot
Arylbenzofurans from Dalbergia parviflora
inferredcites →https://doi.org/10.1016/0031-9422(88)80700-3openalex-snapshot
Prenylisoflavones from Euchresta japonica
inferredcites →https://doi.org/10.1016/0031-9422(91)80108-dopenalex-snapshot
Two complex flavanones from the roots ofSophora leachiana
inferredcites →https://doi.org/10.1016/0031-9422(91)84251-mopenalex-snapshot
A trifolirhizin malonate from Sophora flavescens var. Angustifolia and its stability
inferredcites →https://doi.org/10.1016/0031-9422(91)85143-nopenalex-snapshot
Isoflavans and a pterocarpan from Astragalus mongholicus
inferredcites →https://doi.org/10.1016/0031-9422(92)90052-ropenalex-snapshot
Coumaronochromones in the roots of Euchresta japonica
inferredcites →https://doi.org/10.1016/0031-9422(93)85477-9openalex-snapshot
Flavonoids and a benzofuran in roots of Euchresta tubulosa
inferredcites →https://doi.org/10.1016/0031-9422(94)00671-fopenalex-snapshot
Prenylated isoflavonoids from Erythrina sensegalensis
inferredcites →https://doi.org/10.1016/0031-9422(94)00788-uopenalex-snapshot
Prenylated isoflavonoids—An update
inferredcites →https://doi.org/10.1016/0031-9422(95)00653-2openalex-snapshot
Antimicrobial isoflavanones from Desmodium canum
inferredcites →https://doi.org/10.1016/0031-9422(95)00684-2openalex-snapshot
Detoxification of the phytoalexins maackiain and medicarpin by fungal pathogens of alfalfa
inferredcites →https://doi.org/10.1016/0031-9422(95)91511-xopenalex-snapshot
Flavonoid compounds in roots of Sophora tetraptera
inferredcites →https://doi.org/10.1016/0031-9422(96)00138-0openalex-snapshot
A pterocarpan from Erythrina orientalis
inferredcites →https://doi.org/10.1016/0031-9422(96)00260-9openalex-snapshot
Colutequinone and colutehydroquinone, antifungal isoflavonoids from Colutea arborescens
inferredcites →https://doi.org/10.1016/0031-9422(96)00346-9openalex-snapshot
Isoflavenes from the roots of Cicer judaicum
inferredcites →https://doi.org/10.1016/0040-4020(61)80016-1openalex-snapshot
Synthetic analogues of wedelolactone
inferredcites →https://doi.org/10.1016/0305-1978(93)90090-eopenalex-snapshot
Flavonoids and isoflavonoids of chemotaxonomic significance from Glycyrrhiza pallidiflora (Leguminosae)
inferredcites →https://doi.org/10.1016/0960-0760(95)00131-iopenalex-snapshot
A urinary profile study of dietary phytoestrogens. The identification and mode of metabolism of new isoflavonoids
inferredcites →https://doi.org/10.1016/j.bbrc.2005.03.053openalex-snapshot
Multiple mutagenesis of P450 isoflavonoid synthase reveals a key active-site residue
inferredcites →https://doi.org/10.1016/j.bmc.2004.06.014openalex-snapshot
Antibacterial prenylflavone derivatives from Psoralea corylifolia, and their structure–activity relationship study
inferredcites →https://doi.org/10.1016/j.bmc.2007.11.027openalex-snapshot
Trypanocidal activity of a new pterocarpan and other secondary metabolites of plants from Northeastern Brazil flora
inferredcites →https://doi.org/10.1016/j.bmcl.2003.11.074openalex-snapshot
Anti-inflammatory flavonoids and pterocarpanoid from Crotalaria pallida and C. assamica
inferredcites →https://doi.org/10.1016/j.bmcl.2007.03.044openalex-snapshot
Glaziovianin A, a new isoflavone, from the leaves of Ateleia glazioviana and its cytotoxic activity against human cancer cells
inferredcites →https://doi.org/10.1016/j.bmcl.2008.01.116openalex-snapshot
Absolute configurations of isoflavan-4-ol stereoisomers
inferredcites →https://doi.org/10.1016/j.bmcl.2008.12.064openalex-snapshot
Osteogenic activity of constituents from Butea monosperma
inferredcites →https://doi.org/10.1016/j.bse.2004.10.015openalex-snapshot
A new isoflavone from Genista saharae (Fabaceae)
inferredcites →https://doi.org/10.1016/j.cclet.2007.01.008openalex-snapshot
A new isoflavonolignan from Pueraria alopecuroides Craib
inferredcites →https://doi.org/10.1016/j.cclet.2007.07.036openalex-snapshot
A new isoflavane from processed Astragalus membranaceus
inferredcites →https://doi.org/10.1016/j.cclet.2008.06.014openalex-snapshot
Two new rotenoids from the root of Derris elliptica
inferredcites →https://doi.org/10.1016/j.chroma.2003.08.001openalex-snapshot
Determination of isoflavones in red clover and related species by high-performance liquid chromatography combined with ultraviolet and mass spectrometric detection
inferredcites →https://doi.org/10.1016/j.chroma.2005.01.015openalex-snapshot
Capillary liquid chromatography–microcoil 1H nuclear magnetic resonance spectroscopy and liquid chromatography–ion trap mass spectrometry for on-line structure elucidation of isoflavones in Radix astragali
inferredcites →https://doi.org/10.1016/j.chroma.2006.01.019openalex-snapshot
Analytical separation and detection methods for flavonoids
inferredcites →https://doi.org/10.1016/j.drudis.2007.10.010openalex-snapshot
Plant-derived compounds in clinical trials
inferredcites →https://doi.org/10.1016/j.febslet.2006.09.016openalex-snapshot
Identification of cDNAs encoding pterocarpan reductase involved in isoflavan phytoalexin biosynthesis in Lotus japonicus by EST mining
inferredcites →https://doi.org/10.1016/j.fitote.2003.07.012openalex-snapshot
New prenylated isoflavanones and other constituents of Lespedeza bicolor
inferredcites →https://doi.org/10.1016/j.fitote.2007.04.007openalex-snapshot
A new isoflavone glucoside from Astragalus membranaceus var. mongholicus
inferredcites →https://doi.org/10.1016/j.jep.2004.04.003openalex-snapshot
Flavonoids of an extract of Pterospartum tridentatum showing endothelial protection against oxidative injury
inferredcites →https://doi.org/10.1016/j.jmb.2006.03.022openalex-snapshot
Crystal Structure of Isoflavone Reductase from Alfalfa (Medicago sativa L.)
inferredcites →https://doi.org/10.1016/j.jmb.2007.05.036openalex-snapshot
Crystal Structure of Medicago truncatula UGT85H2 – Insights into the Structural Basis of a Multifunctional (Iso)flavonoid Glycosyltransferase
inferredcites →https://doi.org/10.1016/j.jpba.2007.04.019openalex-snapshot
Characterization of flavonoids in the extract of Sophora flavescens Ait. by high-performance liquid chromatography coupled with diode-array detector and electrospray ionization mass spectrometry
inferredcites →https://doi.org/10.1016/j.pbi.2006.03.016openalex-snapshot
Acyltransferases in plants: a good time to be BAHD
inferredcites →https://doi.org/10.1016/j.phytochem.2003.08.010openalex-snapshot
Isoflavonoids from Dalbergia olivari
inferredcites →https://doi.org/10.1016/j.phytochem.2003.09.003openalex-snapshot
Prenylated flavonoids from Moghania philippinensis
inferredcites →https://doi.org/10.1016/j.phytochem.2003.09.011openalex-snapshot
Furanoflavonoids from Pongamia pinnata fruits☆
inferredcites →https://doi.org/10.1016/j.phytochem.2003.10.022openalex-snapshot
Horseradish peroxidase: a modern view of a classic enzyme
inferredcites →https://doi.org/10.1016/j.phytochem.2003.11.011openalex-snapshot
Neocandenatone, an isoflavan-cinnamylphenol quinone methide pigment from Dalbergia congestiflora
inferredcites →https://doi.org/10.1016/j.phytochem.2004.02.011openalex-snapshot
Antimicrobial and antioxidant flavonoids from the root wood of Bolusanthus speciosus
inferredcites →https://doi.org/10.1016/j.phytochem.2004.03.006openalex-snapshot
A benzil and isoflavone derivatives from Derris scandens Benth.
inferredcites →https://doi.org/10.1016/j.phytochem.2004.04.030openalex-snapshot
Minor pyrano-isoflavones from Eriosema kraussianum: activity-, structure-, and chemical reaction studies
inferredcites →https://doi.org/10.1016/j.phytochem.2004.10.013openalex-snapshot
Antimicrobial and radical scavenging flavonoids from the stem wood of
inferredcites →https://doi.org/10.1016/j.phytochem.2005.02.002openalex-snapshot
Circular dichroism, a powerful tool for the assessment of absolute configuration of flavonoids
inferredcites →https://doi.org/10.1016/j.phytochem.2005.02.005openalex-snapshot
7a-O-methyldeguelol, a modified rotenoid with an open ring-C, from the roots of Derris trifoliata
inferredcites →https://doi.org/10.1016/j.phytochem.2005.06.024openalex-snapshot
Purification of an isoflavonoid 7-O-β-apiosyl-glucoside β-glycosidase and its substrates from Dalbergia nigrescens Kurz
inferredcites →https://doi.org/10.1016/j.phytochem.2005.09.022openalex-snapshot
Flavones and isoflavones from the west African Fabaceae Erythrina vogelii
inferredcites →https://doi.org/10.1016/j.phytochem.2005.12.027openalex-snapshot
Studies on the late steps of (+) pisatin biosynthesis: Evidence for (−) enantiomeric intermediates
inferredcites →https://doi.org/10.1016/j.phytochem.2006.01.002openalex-snapshot
Two unusual rotenoid derivatives, 7a-O-methyl-12a-hydroxydeguelol and spiro-13-homo-13-oxaelliptone, from the seeds of Derris trifoliata
inferredcites →https://doi.org/10.1016/j.phytochem.2006.01.020openalex-snapshot
Distribution of isoflavonoids in non-leguminous taxa – An update
inferredcites →https://doi.org/10.1016/j.phytochem.2006.03.019openalex-snapshot
Antimycobacterial flavonoids from Derris indica
inferredcites →https://doi.org/10.1016/j.phytochem.2006.09.010openalex-snapshot
Catalytic specificity of pea O-methyltransferases suggests gene duplication for (+)-pisatin biosynthesis
inferredcites →https://doi.org/10.1016/j.phytochem.2006.10.023openalex-snapshot
Metabolic profiling and systematic identification of flavonoids and isoflavonoids in roots and cell suspension cultures of Medicago truncatula using HPLC–UV–ESI–MS and GC–MS
inferredcites →https://doi.org/10.1016/j.phytochem.2006.11.035openalex-snapshot
C-methylated and C-prenylated isoflavonoids from root extract of Desmodium uncinatum
inferredcites →https://doi.org/10.1016/j.phytochem.2007.02.015openalex-snapshot
Isoflavanones and their O-glycosides from Desmodium styracifolium
inferredcites →https://doi.org/10.1016/j.phytochem.2007.04.015openalex-snapshot
Isoflavanones from Uraria picta and their antimicrobial activity
inferredcites →https://doi.org/10.1016/j.phytochem.2007.05.017openalex-snapshot
cDNA cloning of a BAHD acyltransferase from soybean (Glycine max): Isoflavone 7-O-glucoside-6″-O-malonyltransferase
inferredcites →https://doi.org/10.1016/j.phytochem.2007.05.038openalex-snapshot
Rotenoid derivatives and other constituents of the twigs of Millettia duchesnei
inferredcites →https://doi.org/10.1016/j.phytochem.2007.06.013openalex-snapshot
Inactivation of pea genes by RNAi supports the involvement of two similar O-methyltransferases in the biosynthesis of (+)-pisatin and of chiral intermediates with a configuration opposite that found in (+)-pisatin
inferredcites →https://doi.org/10.1016/j.phytochem.2007.07.011openalex-snapshot
Estrogenic constituents of the heartwood of Dalbergia parviflora
inferredcites →https://doi.org/10.1016/j.phytochem.2007.08.006openalex-snapshot
Isoflavonoids in non-leguminous taxa: A rarity or a rule?
inferredcites →https://doi.org/10.1016/j.phytol.2007.11.001openalex-snapshot
O-Prenylated flavonoids from Dalbergia sissoo
inferredcites →https://doi.org/10.1016/j.phytol.2008.09.006openalex-snapshot
Pumilanol, an antiprotozoal isoflavanol from Tephrosia pumila
inferredcites →https://doi.org/10.1016/j.tet.2003.08.015openalex-snapshot
A direct route to isoflavan quinones. The synthesis of colutequinones A and B
inferredcites →https://doi.org/10.1016/j.tet.2006.02.015openalex-snapshot
Synthesis of cicerfuran, an antifungal benzofuran, and some related analogues
inferredcites →https://doi.org/10.1016/j.tetlet.2004.04.010openalex-snapshot
A new cyclooxygenase (COX) inhibitory pterocarpan from Indigofera aspalathoides: structure elucidation and determination of binding orientations in the active sites of the enzyme by molecular docking
inferredcites →https://doi.org/10.1016/j.tetlet.2005.11.069openalex-snapshot
Substituted tubaic acids, new oxidative rotenoid metabolites from Lonchocarpus nicou
inferredcites →https://doi.org/10.1016/j.tetlet.2006.10.034openalex-snapshot
A facile synthesis of isoflavone 7-O-glucuronides
inferredcites →https://doi.org/10.1016/j.tetlet.2008.02.063openalex-snapshot
Nor-dehydrodeguelin and nor-dehydrorotenone, C22 coumaronochromones from Lonchocarpus nicou
inferredcites →https://doi.org/10.1016/j.tetlet.2008.04.003openalex-snapshot
Tonkinensines A and B, two novel alkaloids from Sophora tonkinensis
inferredcites →https://doi.org/10.1016/s0003-2670(01)01370-8openalex-snapshot
Identification of isoflavone conjugates in red clover (Trifolium pratense) by liquid chromatography–mass spectrometry after two-dimensional solid-phase extraction
inferredcites →https://doi.org/10.1016/s0014-5793(98)00866-7openalex-snapshot
Molecular characterization and functional expression of dihydroxypterocarpan 6a‐hydroxylase, an enzyme specific for pterocarpanoid phytoalexin biosynthesis in soybean (Glycine max L.)
inferredcites →https://doi.org/10.1016/s0021-9258(17)31799-4openalex-snapshot
Conversion of vestitone to medicarpin in alfalfa (Medicago sativa L.) is catalyzed by two independent enzymes. Identification, purification, and characterization of vestitone reductase and 7,2‘-dihydroxy-4‘-methoxyisoflavanol dehydratase.
inferredcites →https://doi.org/10.1016/s0021-9673(00)00149-7openalex-snapshot
Liquid chromatography–electrospray ionization mass spectrometry study of the flavonoids of the roots of Astragalus mongholicus and A. membranaceus
inferredcites →https://doi.org/10.1016/s0021-9673(01)01231-6openalex-snapshot
Determination of isoflavone glucoside malonates in Trifolium pratense L. (red clover) extracts: quantification and stability studies
inferredcites →https://doi.org/10.1016/s0021-9673(02)01224-4openalex-snapshot
On-line identification of the antifungal constituents of Erythrina vogelii by liquid chromatography with tandem mass spectrometry, ultraviolet absorbance detection and nuclear magnetic resonance spectrometry combined with liquid chromatographic micro-fractionation
inferredcites →https://doi.org/10.1016/s0021-9673(03)00303-0openalex-snapshot
Liquid chromatography with ultraviolet absorbance–mass spectrometric detection and with nuclear magnetic resonance spectrometry: a powerful combination for the on-line structural investigation of plant metabolites
inferredcites →https://doi.org/10.1016/s0024-3205(02)01864-7openalex-snapshot
Anti-Helicobacter pylori flavonoids from licorice extract
inferredcites →https://doi.org/10.1016/s0031-9422(00)00244-2openalex-snapshot
Minor flavonoids from licorice
inferredcites →https://doi.org/10.1016/s0031-9422(00)00337-xopenalex-snapshot
Flavonoid constituents from Glycyrrhiza glabra hairy root cultures
inferredcites →https://doi.org/10.1016/s0031-9422(00)00349-6openalex-snapshot
Two isoflavanones from the stem bark of Erythrina sacleuxii
inferredcites →https://doi.org/10.1016/s0031-9422(00)00366-6openalex-snapshot
Profiling changes in metabolism of isoflavonoids and their conjugates in Lupinus albus treated with biotic elicitor
inferredcites →https://doi.org/10.1016/s0031-9422(00)00400-3openalex-snapshot
Further isoflavonoid metabolites from Millettia griffoniana (Bail)
inferredcites →https://doi.org/10.1016/s0031-9422(00)00441-6openalex-snapshot
Erysubins C–F, four isoflavonoids from Erythrina suberosa var. glabrescences
inferredcites →https://doi.org/10.1016/s0031-9422(00)83844-3openalex-snapshot
Two isoflavonoids from the fresh bulbs of Iris tingitana
inferredcites →https://doi.org/10.1016/s0031-9422(00)90378-9openalex-snapshot
Anti-oral microbial activity of isoflavonoids in root bark of Ormosia monosperma
inferredcites →https://doi.org/10.1016/s0031-9422(00)90776-3openalex-snapshot
Relevance of seed polysaccharides and flavonoids for the classification of the leguminosae: A chemotaxonomic approach
inferredcites →https://doi.org/10.1016/s0031-9422(00)98023-3openalex-snapshot
Coumaronochromones from the stems of Euschresta formosana
inferredcites →https://doi.org/10.1016/s0031-9422(00)98095-6openalex-snapshot
Six flavanones from the roots of Euchresta formosana
inferredcites →https://doi.org/10.1016/s0031-9422(00)98260-8openalex-snapshot
Four flavonoids in the roots of Euchresta Formosana
inferredcites →https://doi.org/10.1016/s0031-9422(01)00009-7openalex-snapshot
Flavonoids from the stem bark of Bolusanthus speciosus
inferredcites →https://doi.org/10.1016/s0031-9422(01)00111-xopenalex-snapshot
A heartwood pigment in Dalbergia cell cultures
inferredcites →https://doi.org/10.1016/s0031-9422(01)00195-9openalex-snapshot
Isoflavonoid glycosides from Dalbergia sissoo
inferredcites →https://doi.org/10.1016/s0031-9422(01)00268-0openalex-snapshot
Flavonoids from Glycyrrhiza pallidiflora hairy root cultures
inferredcites →https://doi.org/10.1016/s0031-9422(01)00295-3openalex-snapshot
Andinermals A–C, antiplasmodial constituents from Andira inermis
inferredcites →https://doi.org/10.1016/s0031-9422(01)00368-5openalex-snapshot
Cytotoxic isoflavones from Erythrina indica
inferredcites →https://doi.org/10.1016/s0031-9422(01)00459-9openalex-snapshot
Three isoflav-3-enes and a 2-arylbenzofuran from the root bark of Erythrina burttii
inferredcites →https://doi.org/10.1016/s0031-9422(01)00462-9openalex-snapshot
An isoflavanoid–neoflavonoid and an O-methylated isoflavone from the heartwood of Dalbergia nitidula
inferredcites →https://doi.org/10.1016/s0031-9422(02)00017-1openalex-snapshot
Coumaronochromones and flavanones from Euchresta formosana roots
inferredcites →https://doi.org/10.1016/s0031-9422(02)00035-3openalex-snapshot
Pyrano-isoflavones with erectile-dysfunction activity from Eriosema kraussianum
inferredcites →https://doi.org/10.1016/s0031-9422(02)00078-xopenalex-snapshot
Flavonoids from Tephrosia aequilata
inferredcites →https://doi.org/10.1016/s0031-9422(02)00093-6openalex-snapshot
Flavonoids from Glycyrrhiza pallidiflora hairy root cultures
inferredcites →https://doi.org/10.1016/s0031-9422(02)00163-2openalex-snapshot
Isoflavone glycosides from Derris scandens
inferredcites →https://doi.org/10.1016/s0031-9422(02)00164-4openalex-snapshot
Isoflavonoids from the roots of Erythrina poeppigiana
inferredcites →https://doi.org/10.1016/s0031-9422(02)00202-9openalex-snapshot
Prenylated flavonoids of Erythrina lysistemon grown in Egypt
inferredcites →https://doi.org/10.1016/s0031-9422(02)00489-2openalex-snapshot
Prenylated isoflavonoids from Millettia pervilleana
inferredcites →https://doi.org/10.1016/s0031-9422(02)00621-0openalex-snapshot
Recent findings on natural products with erectile-dysfunction activity
inferredcites →https://doi.org/10.1016/s0031-9422(02)00671-4openalex-snapshot
Efficient production and capture of 8-prenylnaringenin and leachianone G—biosynthetic intermediates of sophoraflavanone G—by the addition of cork tissue to cell suspension cultures of Sophora flavescens
inferredcites →https://doi.org/10.1016/s0031-9422(03)00184-5openalex-snapshot
An arylbenzofuran and four isoflavonoids from the roots of Erythrina poeppigiana
inferredcites →https://doi.org/10.1016/s0031-9422(03)00190-0openalex-snapshot
Pterocarpans from Bituminaria morisiana and Bituminaria bituminosa
inferredcites →https://doi.org/10.1016/s0031-9422(03)00201-2openalex-snapshot
Three isoflavanones with cannabinoid-like moieties from Desmodium canum
inferredcites →https://doi.org/10.1016/s0031-9422(03)00209-7openalex-snapshot
Two prenylated flavonoids from the stem bark of Erythrina burttii
inferredcites →https://doi.org/10.1016/s0031-9422(03)00324-8openalex-snapshot
Isoflavanones from the allelopathic aqueous root exudate of Desmodium uncinatum
inferredcites →https://doi.org/10.1016/s0031-9422(03)00373-xopenalex-snapshot
Anti-plasmodial activities and X-ray crystal structures of rotenoids from Millettia usaramensis subspecies usaramensis
inferredcites →https://doi.org/10.1016/s0031-9422(03)00390-xopenalex-snapshot
Isoflavonoids from roots of Erythrina zeyheri
inferredcites →https://doi.org/10.1016/s0031-9422(96)00391-3openalex-snapshot
Isoprenylated flavonoids from underground parts of Glycyrrhiza glabra
inferredcites →https://doi.org/10.1016/s0031-9422(96)00582-1openalex-snapshot
Isoflavanones in roots of Sophora secundiflora
inferredcites →https://doi.org/10.1016/s0031-9422(96)00757-1openalex-snapshot
2-Methoxyjudaicin, an isoflavene from the roots of Cicer bijugum
inferredcites →https://doi.org/10.1016/s0031-9422(96)00773-xopenalex-snapshot
Two prenylated isoflavanones from Millettia pervilleana
inferredcites →https://doi.org/10.1016/s0031-9422(96)00841-2openalex-snapshot
A pterocarpan from Erythrina orientalis
inferredcites →https://doi.org/10.1016/s0031-9422(97)00071-xopenalex-snapshot
Three pterocarpans from Erythrina crista-galli
inferredcites →https://doi.org/10.1016/s0031-9422(97)00097-6openalex-snapshot
Pubescidin, an isoflavone glycoside from Centrosema pubescens
inferredcites →https://doi.org/10.1016/s0031-9422(97)00326-9openalex-snapshot
An O-geranylated isoflavone from Millettia griffoniana
inferredcites →https://doi.org/10.1016/s0031-9422(97)00338-5openalex-snapshot
4′-dehydroxycabenegrin A-I from roots of Harpalyce brasiliana
inferredcites →https://doi.org/10.1016/s0031-9422(97)00371-3openalex-snapshot
Phenolic glucosides from the root of Pueraria lobata
inferredcites →https://doi.org/10.1016/s0031-9422(97)00405-6openalex-snapshot
Dimethylchromene rotenoids from Tephrosia candida
inferredcites →https://doi.org/10.1016/s0031-9422(97)00424-xopenalex-snapshot
Rotenoids, isoflavones and chalcones from the stem bark of Millettia usaramensis subspecies usaramensis
inferredcites →https://doi.org/10.1016/s0031-9422(97)00474-3openalex-snapshot
Flavonoids from the root and stem of Sophora tomentosa
inferredcites →https://doi.org/10.1016/s0031-9422(97)00517-7openalex-snapshot
Isoflavonoids and a pterocarpan from Gliricidia sepium
inferredcites →https://doi.org/10.1016/s0031-9422(97)00518-9openalex-snapshot
Conrauinones C and D, two isoflavones from stem bark of Millettia conraui
inferredcites →https://doi.org/10.1016/s0031-9422(97)00537-2openalex-snapshot
Clitoriacetal 11-O-β-d-glucopyranoside from Clitoria fairchildiana
inferredcites →https://doi.org/10.1016/s0031-9422(97)00560-8openalex-snapshot
Acylated flavonoid glycosides and accompanying phenolics from licorice
inferredcites →https://doi.org/10.1016/s0031-9422(97)00591-8openalex-snapshot
Isoprenylated flavonoids from hairy root cultures of Glycyrrhiza glabra
inferredcites →https://doi.org/10.1016/s0031-9422(97)00596-7openalex-snapshot
Two pterocarpans from Erythrina orientalis
inferredcites →https://doi.org/10.1016/s0031-9422(97)00633-xopenalex-snapshot
Three prenylated isoflavans from Maackia tenuifolia
inferredcites →https://doi.org/10.1016/s0031-9422(97)00732-2openalex-snapshot
An isoflavan from Erythrina x bidwillii
inferredcites →https://doi.org/10.1016/s0031-9422(97)00798-xopenalex-snapshot
The distribution of isoflavonoids in cicer
inferredcites →https://doi.org/10.1016/s0031-9422(97)00802-9openalex-snapshot
Isoflavonoids from Sophora secundiflora, S. arizonica and S. gypsophila
showing the first 200 of 507 · page through all 507

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Chemosystematic and evolutionary trends of the genistoid clade sensu stricto (Papilionoideae, Fabaceae)
inferred← citeshttps://doi.org/10.2139/ssrn.3928330openalex-extracted
Amphimas pterocarpoides Harms: An Evaluation of Flavonoid and Phenolic Contents, Wound Healing, Anthelmintic and Antioxidant Activities of the Leaves and Stem Bark
inferred← citeshttps://doi.org/10.1002/9781444323375.ch2openalex-snapshot
Flavonoid Chemistry of the Leguminosae
inferred← citeshttps://doi.org/10.1002/advs.202413851openalex-snapshot
N‐Heterocyclic Carbene Organocatalysis Enabled Modular Synthesis of Fluorinated Isoflavonoids to Suppress Proliferation and Migration in Breast Cancer Cells
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Palladium‐Catalyzed Highly Chemoselective Cascade Coupling‐Cyclization of Allenol Derivatives and Aryl Halides for the Construction of Dihydrobenzofuranols or Chromanols and Indolinols
inferred← citeshttps://doi.org/10.1002/ange.201901801openalex-snapshot
Asymmetric Lewis Acid Catalyzed Electrochemical Alkylation
inferred← citeshttps://doi.org/10.1002/anie.201901801openalex-snapshot
Asymmetric Lewis Acid Catalyzed Electrochemical Alkylation
inferred← citeshttps://doi.org/10.1002/bkcs.10806openalex-snapshot
An Efficient and Versatile Synthesis of Isoflavones from 2‐Methoxybenzoic Acids
inferred← citeshttps://doi.org/10.1002/cctc.202101252openalex-snapshot
Enantioselective Synthesis of Isoflavanones and Pterocarpans through a RuII‐Catalyzed ATH‐DKR of Isoflavones
inferred← citeshttps://doi.org/10.1002/cctc.202101740openalex-snapshot
Cover Feature: Enantioselective Synthesis of Isoflavanones and Pterocarpans through a RuII‐Catalyzed ATH‐DKR of Isoflavones (ChemCatChem 24/2021)
inferred← citeshttps://doi.org/10.1002/chin.200730267openalex-snapshot
Isoflavonoids of the Leguminosae
inferred← citeshttps://doi.org/10.1002/ece3.71895openalex-snapshot
Combining Niche Breadth to Predict the Current and Future Distribution of Leguminosae Under Climate Change on the Qinghai‐Xizang Plateau
inferred← citeshttps://doi.org/10.1002/ejoc.201101228openalex-snapshot
Asymmetric Methods for the Synthesis of Flavanones, Chromanones, and Azaflavanones
inferred← citeshttps://doi.org/10.1002/jhet.4158openalex-snapshot
A concise route towards isoflavans
inferred← citeshttps://doi.org/10.1002/ptr.7852openalex-snapshot
Pharmacokinetics, pharmacodynamics, toxicity, and formulations of daidzein: An important isoflavone
inferred← citeshttps://doi.org/10.1002/tcr.201700069openalex-snapshot
Combination of Tetrabutylammonium Iodide (TBAI) with tert ‐Butyl Hydroperoxide (TBHP): An Efficient Transition‐Metal‐Free System to Construct Various Chemical Bonds
inferred← citeshttps://doi.org/10.1007/978-3-030-51034-3_2openalex-snapshot
Specialized Metabolites and Plant Defence
inferred← citeshttps://doi.org/10.1007/978-3-030-58975-2_14openalex-snapshot
Phytochemistry, Pharmacology, and Pharmacokinetics of Phytoestrogens from Red Clover Extract: An Exhaustive Overview
inferred← citeshttps://doi.org/10.1007/978-3-030-74768-8_11openalex-snapshot
Biosynthesis of Phenolic Antioxidants
inferred← citeshttps://doi.org/10.1007/978-3-319-27490-4_30-1openalex-snapshot
Metabolic Engineering of PhenylPropanoids in Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-96932-9_1openalex-snapshot
Common Bean Genetics, Breeding, and Genomics for Adaptation to Changing to New Agri-environmental Conditions
inferred← citeshttps://doi.org/10.1007/978-3-642-22144-6_57openalex-snapshot
Phenolic Compounds: Introduction
inferred← citeshttps://doi.org/10.1007/978-94-007-1933-0_5openalex-snapshot
Secondary Metabolites and Plant Defence
inferred← citeshttps://doi.org/10.1007/978-94-007-4749-4_7openalex-snapshot
The Medicago truncatula Gene Expression Atlas (MtGEA): A Tool for Legume Seed Biology and Biotechnology
inferred← citeshttps://doi.org/10.1007/978-981-99-2302-1_13openalex-snapshot
Recent Progress in the Pharmacology of Phytoestrogens: Emerging Neuromodulators for Treating Anxiety and Depression
inferred← citeshttps://doi.org/10.1007/s00210-024-03356-5openalex-snapshot
Daidzein’s potential in halting neurodegeneration: unveiling mechanistic insights
inferred← citeshttps://doi.org/10.1007/s00253-010-2512-8openalex-snapshot
Genetic and metabolic engineering of isoflavonoid biosynthesis
inferred← citeshttps://doi.org/10.1007/s00253-024-13254-8openalex-snapshot
Prenylation of aromatic amino acids and plant phenolics by an aromatic prenyltransferase from Rasamsonia emersonii
inferred← citeshttps://doi.org/10.1007/s00299-014-1733-1openalex-snapshot
De novo transcriptome sequencing in Pueraria lobata to identify putative genes involved in isoflavones biosynthesis
inferred← citeshttps://doi.org/10.1007/s00299-016-2006-yopenalex-snapshot
Metabolite fingerprinting, pathway analyses, and bioactivity correlations for plant species belonging to the Cornaceae, Fabaceae, and Rosaceae families
inferred← citeshttps://doi.org/10.1007/s00425-023-04136-wopenalex-snapshot
Advances in the study of the function and mechanism of the action of flavonoids in plants under environmental stresses
inferred← citeshttps://doi.org/10.1007/s00606-012-0726-1openalex-snapshot
Isoflavone synthase (IFS) gene phylogeny in Trifolium species associated with plant isoflavone contents
inferred← citeshttps://doi.org/10.1007/s10068-022-01070-7openalex-snapshot
Current perspectives on the beneficial effects of soybean isoflavones and their metabolites on plants
inferred← citeshttps://doi.org/10.1007/s10535-013-0344-yopenalex-snapshot
Functional expression and subcellular localization of pea polymorphic isoflavone synthase CYP93C18
inferred← citeshttps://doi.org/10.1007/s10562-023-04276-4openalex-snapshot
Palladium(II) Pincer Type Complexes Containing ONO Donor Heterocyclic Hydrazones: Synthesis, Structure and Catalytic Activity Towards the Suzuki–Miyaura Cross-Coupling of 3-Bromochromone and Arylboronic Acids via C–Br Activation
inferred← citeshttps://doi.org/10.1007/s10681-013-0949-4openalex-snapshot
Screening for resistance to clover rot (Sclerotinia spp.) among a diverse collection of red clover populations (Trifolium pratense L.)
inferred← citeshttps://doi.org/10.1007/s11101-015-9400-xopenalex-snapshot
Phytochemical analysis of isoflavonoids using liquid chromatography coupled with tandem mass spectrometry
inferred← citeshttps://doi.org/10.1007/s11101-018-9586-9openalex-snapshot
The phenolic profile of pea (Pisum sativum): a phytochemical and pharmacological overview
inferred← citeshttps://doi.org/10.1007/s11101-022-09811-6openalex-snapshot
Trends in the biotechnological production of isoflavonoids in plant cell suspension cultures
inferred← citeshttps://doi.org/10.1007/s11101-022-09845-wopenalex-snapshot
Millettia isoflavonoids: a comprehensive review of structural diversity, extraction, isolation, and pharmacological properties
inferred← citeshttps://doi.org/10.1007/s11306-011-0287-2openalex-snapshot
LC/MS profiling of flavonoid glycoconjugates isolated from hairy roots, suspension root cell cultures and seedling roots of Medicago truncatula
inferred← citeshttps://doi.org/10.1007/s11306-012-0475-8openalex-snapshot
Changes of phenolic secondary metabolite profiles in the reaction of narrow leaf lupin (Lupinus angustifolius) plants to infections with Colletotrichum lupini fungus or treatment with its toxin
inferred← citeshttps://doi.org/10.1007/s11434-015-0929-2openalex-snapshot
Recent advances in biosynthesis of bioactive compounds in traditional Chinese medicinal plants
inferred← citeshttps://doi.org/10.1007/s11816-021-00711-3openalex-snapshot
An insight into in vitro strategies for bioproduction of isoflavones
inferred← citeshttps://doi.org/10.1007/s13258-011-0043-zopenalex-snapshot
Novel major quantitative trait loci regulating the content of isoflavone in soybean seeds
inferred← citeshttps://doi.org/10.1007/s13592-021-00889-zopenalex-snapshot
How diverse is the chemistry and plant origin of Brazilian propolis?
inferred← citeshttps://doi.org/10.1007/s13659-017-0121-2openalex-snapshot
Polysubstituted Isoflavonoids from Spatholobus suberectus, Flemingia macrophylla, and Cudrania cochinchinensis
inferred← citeshttps://doi.org/10.1007/s13659-026-00627-xopenalex-snapshot
Advances in natural coumaronochromones: a comprehensive review of natural occurrence, bioactivities, and chemical synthesis
inferred← citeshttps://doi.org/10.1016/b978-0-08-102227-6.00004-8openalex-snapshot
Chemistry of Himalayan Phytochemicals
inferred← citeshttps://doi.org/10.1016/b978-0-12-411462-3.00039-4openalex-snapshot
Neuroprotection by Dietary Isoflavones and Their Role in Cerebral Ischemia
inferred← citeshttps://doi.org/10.1016/b978-0-12-821038-3.00045-8openalex-snapshot
Isoflavones: toxicological aspects and efficacy
inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00023-xopenalex-snapshot
Plant Phenolics: Phenylpropanoids
inferred← citeshttps://doi.org/10.1016/j.bcab.2013.09.004openalex-snapshot
Biotransformation for multiple regio-selective hydroxylation of isoflavonoid
inferred← citeshttps://doi.org/10.1016/j.bcp.2014.09.027openalex-snapshot
Antagonism of human formyl peptide receptor 1 (FPR1) by chromones and related isoflavones
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2016.02.012openalex-snapshot
Microbial production of natural and non-natural flavonoids: Pathway engineering, directed evolution and systems/synthetic biology
inferred← citeshttps://doi.org/10.1016/j.bjp.2018.08.004openalex-snapshot
Antifungal activity of extracts and phenolic compounds from Deguelia duckeana
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.03.055openalex-snapshot
Synthesis and biological evaluation of isoflavone fatty acid esters with potential weight loss and hypolipidemic activities
inferred← citeshttps://doi.org/10.1016/j.bse.2010.12.024openalex-snapshot
Sulphur compounds from the aerial parts of Eclipta prostrata
inferred← citeshttps://doi.org/10.1016/j.bse.2012.07.006openalex-snapshot
Chemical constituents from bark of Millettia mannii Baker (Papilionoideae−Leguminosae)
inferred← citeshttps://doi.org/10.1016/j.bse.2012.08.002openalex-snapshot
Immunochemical and HPLC identification of isoflavonoids in the Apiaceae family
inferred← citeshttps://doi.org/10.1016/j.cclet.2026.112531openalex-snapshot
Identification of a BBE-like enzyme involved in the biosynthesis of pyranocoumarins and its catalytic mechanism in the pyran ring formation
inferred← citeshttps://doi.org/10.1016/j.chembiol.2010.03.010openalex-snapshot
A Versatile Microbial System for Biosynthesis of Novel Polyphenols with Altered Estrogen Receptor Binding Activity
inferred← citeshttps://doi.org/10.1016/j.comtox.2022.100247openalex-snapshot
Potential inhibitory activity of phytoconstituents against black fungus: In silico ADMET, molecular docking and MD simulation studies
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2014.07.013openalex-snapshot
Evidence of calycosin-7-O-β-d-glucoside's role as a major antioxidant molecule of Astragalus membranaceus Bge. var. mongholicus (Bge.) Hsiao plants under freezing stress
inferred← citeshttps://doi.org/10.1016/j.fitote.2013.07.003openalex-snapshot
Phytochemistry and biological properties of glabridin
inferred← citeshttps://doi.org/10.1016/j.fitote.2014.03.026openalex-snapshot
Five new prenylated chalcones from Desmodium renifolium
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.04.003openalex-snapshot
Cytotoxic polyphenolic compounds from Lespedeza bicolor stem bark
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106687openalex-snapshot
Brazilian propolis: Chemical composition, regional variability, and bioactive potential
inferred← citeshttps://doi.org/10.1016/j.foodchem.2012.03.028openalex-snapshot
Isoflavone determination in spontaneous legumes identified by DNA barcodes
inferred← citeshttps://doi.org/10.1016/j.foodchem.2015.09.110openalex-snapshot
Variation in accumulation of isoflavonoids in Phaseoleae seedlings elicited by Rhizopus
inferred← citeshttps://doi.org/10.1016/j.foodchem.2017.07.074openalex-snapshot
Rapid membrane permeabilization of Listeria monocytogenes and Escherichia coli induced by antibacterial prenylated phenolic compounds from legumes
inferred← citeshttps://doi.org/10.1016/j.foodchem.2021.131846openalex-snapshot
In-depth phytochemical and biological studies on potential AChE inhibitors in red and zigzag clover dry extracts using reversed–phase liquid chromatography (RP-LC) coupled with photodiode array (PDA) and electron spray ionization-quadrupole/time of flight-mass spectrometric (ESI-QToF/MS-MS)…
inferred← citeshttps://doi.org/10.1016/j.heliyon.2018.e00656openalex-snapshot
Development stage, storage temperature and storage duration influence phytonutrient content in cowpea (Vigna unguiculata L. Walp.)
inferred← citeshttps://doi.org/10.1016/j.heliyon.2020.e03918openalex-snapshot
Preliminary screening of the aqueous extracts of twenty-three different seaweed species in Sri Lanka with in-vitro and in-vivo assays
inferred← citeshttps://doi.org/10.1016/j.heliyon.2021.e08261openalex-snapshot
Amphimas pterocarpoides harms.: An Evaluation of flavonoid and phenolic contents, wound healing, anthelmintic and antioxidant activities of the leaves and stem bark
inferred← citeshttps://doi.org/10.1016/j.ibmb.2010.12.009openalex-snapshot
A substrate-specific cytochrome P450 monooxygenase, CYP6AB11, from the polyphagous navel orangeworm (Amyelois transitella)
inferred← citeshttps://doi.org/10.1016/j.indcrop.2016.06.007openalex-snapshot
Ulex europaeus: from noxious weed to source of valuable isoflavones and flavanones
inferred← citeshttps://doi.org/10.1016/j.indcrop.2019.111792openalex-snapshot
Promising strategy for improving calycosin-7-O-β-D-glucoside production in Astragalus membranaceus adventitious root cultures
inferred← citeshttps://doi.org/10.1016/j.indcrop.2021.113688openalex-snapshot
Specialized metabolite profiling of different Glycyrrhiza glabra organs by untargeted UHPLC-HRMS
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2008.07.298openalex-snapshot
Isoflavonoid composition of the Maackia amurensis callus culture
inferred← citeshttps://doi.org/10.1016/j.jep.2017.06.005openalex-snapshot
Emmenagogue properties of Milicia excelsa (Welw.) C.C. Berg (Moraceae) based, at least in part, on its ability to correlate the activity of the hypothalamic-pituitary axis to that of the ovaries
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2013.06.003openalex-snapshot
Recent advances in understanding the anti-diabetic actions of dietary flavonoids
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2022.109250openalex-snapshot
Estrogenic flavonoids and their molecular mechanisms of action
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2014.08.027openalex-snapshot
Ferrocenyl derivatives of pterocarpene and coumestan: Synthesis, structure and anticancer activity studies
inferred← citeshttps://doi.org/10.1016/j.jpba.2013.05.012openalex-snapshot
Investigation of transport of genistein, daidzein and their inclusion complexes prepared with different cyclodextrins on Caco-2 cell line
inferred← citeshttps://doi.org/10.1016/j.jsbmb.2015.11.020openalex-snapshot
Glyceollins and dehydroglyceollins isolated from soybean act as SERMs and ER subtype-selective phytoestrogens
inferred← citeshttps://doi.org/10.1016/j.molp.2019.06.001openalex-snapshot
The Structure and Function of Major Plant Metabolite Modifications
inferred← citeshttps://doi.org/10.1016/j.mycmed.2017.07.006openalex-snapshot
Anti-dermatophyte activity of Leguminosae plants from Southern Brazil with emphasis on Mimosa pigra (Leguminosae)
inferred← citeshttps://doi.org/10.1016/j.pbi.2014.03.007openalex-snapshot
The chemical logic of plant natural product biosynthesis
inferred← citeshttps://doi.org/10.1016/j.physa.2009.03.011openalex-snapshot
Heterogeneous distribution of metabolites across plant species
inferred← citeshttps://doi.org/10.1016/j.phytochem.2007.08.006openalex-snapshot
Isoflavonoids in non-leguminous taxa: A rarity or a rule?
inferred← citeshttps://doi.org/10.1016/j.phytochem.2012.04.004openalex-snapshot
Rapid isolation and identification of minor natural products by LC–MS, LC–SPE–NMR and ECD: Isoflavanones, biflavanones and bisdihydrocoumarins from Ormocarpum kirkii
inferred← citeshttps://doi.org/10.1016/j.phytochem.2015.12.015openalex-snapshot
Compositional changes in (iso)flavonoids and estrogenic activity of three edible Lupinus species by germination and Rhizopus-elicitation
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113249openalex-snapshot
Bioactive pterocarpans from the root of Astragalus membranaceus var. mongholicus
inferred← citeshttps://doi.org/10.1016/j.phytol.2010.12.005openalex-snapshot
Development of sorbents for immunoaffinity extraction of isoflavonoids
inferred← citeshttps://doi.org/10.1016/j.phytol.2014.05.013openalex-snapshot
Chevalierinoside B and C: Two new isoflavonoid glycosides from the stem bark of Antidesma laciniatum Muell. Arg (syn. Antidesma chevalieri Beille)
inferred← citeshttps://doi.org/10.1016/j.plaphy.2016.11.009openalex-snapshot
UPLC-QTOF analysis reveals metabolomic changes in the flag leaf of wheat ( Triticum aestivum L.) under low-nitrogen stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.11.046openalex-snapshot
Comprehensive identification and characterization of abiotic stress and hormone responsive glycosyl hydrolase family 1 genes in Medicago truncatula
inferred← citeshttps://doi.org/10.1016/j.procbio.2016.01.012openalex-snapshot
Tremendous enhancements of isoflavonoid biosynthesis, associated gene expression and antioxidant capacity in Astragalus membranaceus hairy root cultures elicited by methyl jasmonate
inferred← citeshttps://doi.org/10.1016/j.stress.2023.100153openalex-snapshot
Biosynthesis and role of isoflavonoids in legumes under different environmental conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2009.10.116openalex-snapshot
Synthetic access to optically active isoflavans by using allylic substitution
inferred← citeshttps://doi.org/10.1016/j.tet.2011.09.042openalex-snapshot
Total synthesis of the pyranocoumaronochromone lupinalbin H
inferred← citeshttps://doi.org/10.1016/j.tet.2018.03.004openalex-snapshot
A chiral pool approach for asymmetric syntheses of both antipodes of equol and sativan
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132048openalex-snapshot
Facile synthesis of coumaronochromones through palladium-catalyzed intramolecular cross dehydrogenative coupling
inferred← citeshttps://doi.org/10.1016/j.tetasy.2016.09.002openalex-snapshot
Chiral discrimination of natural isoflavanones using (R)- and (S)-BINOL as the NMR chiral solvating agents
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.04.150openalex-snapshot
A simple approach to highly functionalized benzo[b]furans from phenols and aryl iodides via aryl propargyl ethers
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.06.085openalex-snapshot
New synthetic route to (S)-(−)-equol through allylic substitution
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.01.004openalex-snapshot
Synthesis of 5-deoxypterocarpens, pterocarpens, and coumestans by intramolecular Heck reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.01.151openalex-snapshot
Synthesis of novel electron-deficient chromone-fused dienes via phosphine catalyzed [4+2] annulation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.05.121openalex-snapshot
Synthesis of 6a-hydroxypterocarpans via intramolecular benzoin condensation
inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100730openalex-snapshot
The GmSTF1/2–GmBBX4 negative feedback loop acts downstream of blue-light photoreceptors to regulate isoflavonoid biosynthesis in soybean
inferred← citeshttps://doi.org/10.1016/s0959-6380(09)70019-4openalex-snapshot
Chapter 6.4 (2006): Six-membered ring systems: with O and/or S atoms
inferred← citeshttps://doi.org/10.1016/s0959-6380(09)70020-0openalex-snapshot
Chapter 6.4 (2007): Six-membered ring systems: with O and/or S atoms
inferred← citeshttps://doi.org/10.1016/s1672-6529(16)60295-0openalex-snapshot
Wetting characterizations of oilseed rapes
inferred← citeshttps://doi.org/10.1016/s2221-1691(12)60522-xopenalex-snapshot
An insight on genistein as potential pharmacological and therapeutic agent
inferred← citeshttps://doi.org/10.1016/s2222-1808(12)60134-0openalex-snapshot
Phytochemical characterization of brown seaweed Sargassum wightii
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c02709openalex-snapshot
Primary and Secondary Metabolites in Lotus japonicus
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c02061openalex-snapshot
Comprehensive Quantification of (Poly)phenols in Lotus japonicus with and without Arbuscular Mycorrhizal Symbiosis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00932openalex-snapshot
Total Syntheses of Prenylated Isoflavones from Erythrina sacleuxii and Their Antibacterial Activity: 5-Deoxy-3′-prenylbiochanin A and Erysubin F
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00628openalex-snapshot
Standardized LC×LC-ELSD Fractionation Procedure for the Identification of Minor Bioactives via the Enzymatic Screening of Natural Extracts
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00411openalex-snapshot
Prenylated Isoflavones Originating from East African Medicinal Plants Selectively Modulate the α-Glucosidase from Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00681openalex-snapshot
Synthesis of Isoflavones by Tandem Demethylation and Ring-Opening/Cyclization of Methoxybenzoylbenzofurans
inferred← citeshttps://doi.org/10.1021/acs.joc.0c03024openalex-snapshot
Temperature- and Reagent-Controlled ComplementarySyn- andAnti-Selective Enolboration–Aldolization of Substituted Phenylacetates
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01375openalex-snapshot
Scope and Applications of 2,3-Oxidative Aryl Rearrangements for the Synthesis of Isoflavone Natural Products
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02698openalex-snapshot
The Suzuki–Miyaura Cross-Coupling–Claisen Rearrangement–Cross-Metathesis Approach to Prenylated Isoflavones
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00106openalex-snapshot
Gallium-Catalyzed Domino Arylation/Oxycyclization of Allenes with Phenols
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01941openalex-snapshot
Metal-Free Coupling of 2-Vinylphenols and Carboxylic Acids: An Access to 3-Acyloxy-2,3-dihydrobenzofurans
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00817openalex-snapshot
De Novo Syntheses of Coumaronochromones: Application in Total Synthesis of Cristatone II
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01218openalex-snapshot
Enantioselective Synthesis of Isoflavanones by Catalytic Dynamic Kinetic Resolution
inferred← citeshttps://doi.org/10.1021/acschembio.7b00624openalex-snapshot
Biosynthesis of (−)-5-Hydroxy-equol and 5-Hydroxy-dehydroequol from Soy Isoflavone, Genistein Using Microbial Whole Cell Bioconversion
inferred← citeshttps://doi.org/10.1021/acsomega.5c00866openalex-snapshot
Target Isolation of Prenylated Isoflavonoids and Pterocarpans from Acosmium diffusissimum Using LC–MS/MS-Based Molecular Networking
inferred← citeshttps://doi.org/10.1021/ja401731dopenalex-snapshot
Sequential C–H Functionalization Reactions for the Enantioselective Synthesis of Highly Functionalized 2,3-Dihydrobenzofurans
inferred← citeshttps://doi.org/10.1021/jacs.5c02235openalex-snapshot
Deracemization of C(sp3)–H Arylated Carbonyl Compounds via Asymmetric Ion-Pairing Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/jf2010707openalex-snapshot
Increasing Soy Isoflavonoid Content and Diversity by Simultaneous Malting and Challenging by a Fungus to Modulate Estrogenicity
inferred← citeshttps://doi.org/10.1021/jf3006905openalex-snapshot
Quantitation of Flavanols, Proanthocyanidins, Isoflavones, Flavanones, Dihydrochalcones, Stilbenes, Benzoic Acid Derivatives Using Ultraviolet Absorbance after Identification by Liquid Chromatography–Mass Spectrometry
inferred← citeshttps://doi.org/10.1021/jf3021514openalex-snapshot
Germination Dramatically Increases Isoflavonoid Content and Diversity in Chickpea (Cicer arietinum L.) Seeds
inferred← citeshttps://doi.org/10.1021/jf4020203openalex-snapshot
Modulation of Isoflavonoid Composition of Rhizopus oryzae Elicited Soybean (Glycine max) Seedlings by Light and Wounding
inferred← citeshttps://doi.org/10.1021/jf801227qopenalex-snapshot
Isoflavonoid Composition of a Callus Culture of the Relict Tree Maackia amurensis Rupr. et Maxim
inferred← citeshttps://doi.org/10.1021/np4000763openalex-snapshot
Fungal ABC Transporter-Associated Activity of Isoflavonoids from the Root Extract of Dalea formosa
inferred← citeshttps://doi.org/10.1021/np500016zopenalex-snapshot
HPLC-Based Activity Profiling for GABAA Receptor Modulators in Adenocarpus cincinnatus
inferred← citeshttps://doi.org/10.1021/np900271mopenalex-snapshot
Isoflavonoids from Erythrina poeppigiana: Evaluation of Their Binding Affinity for the Estrogen Receptor
inferred← citeshttps://doi.org/10.1038/s41467-021-26361-1openalex-snapshot
De novo biosynthesis of bioactive isoflavonoids by engineered yeast cell factories
inferred← citeshttps://doi.org/10.1038/s41467-023-42393-1openalex-snapshot
Insights into the missing apiosylation step in flavonoid apiosides biosynthesis of Leguminosae plants
inferred← citeshttps://doi.org/10.1038/s41589-025-01914-3openalex-snapshot
Glyceollin biosynthesis in a plant chassis engineered for isoflavone production
inferred← citeshttps://doi.org/10.1038/s41598-021-92964-9openalex-snapshot
Insights into the molecular properties underlying antibacterial activity of prenylated (iso)flavonoids against MRSA
inferred← citeshttps://doi.org/10.1038/s41598-025-98782-7openalex-snapshot
Unraveling the molecular drivers of antibacterial prenylated (iso)flavonoids and chalcones against Streptococcus mutans
inferred← citeshttps://doi.org/10.1039/b616809bopenalex-snapshot
Isoflavonoids of the Leguminosae
inferred← citeshttps://doi.org/10.1039/b718040nopenalex-snapshot
Flavonoids and their glycosides, including anthocyanins
inferred← citeshttps://doi.org/10.1039/c0np00042fopenalex-snapshot
What every chemist should know about plant names
inferred← citeshttps://doi.org/10.1039/c2fo10290kopenalex-snapshot
Prenylated isoflavonoids from plants as selective estrogen receptor modulators (phytoSERMs)
inferred← citeshttps://doi.org/10.1039/c3np70024kopenalex-snapshot
Isoflavonoids of the Leguminosae
inferred← citeshttps://doi.org/10.1039/c3np70104bopenalex-snapshot
Natural product biosynthesis in Medicago species
inferred← citeshttps://doi.org/10.1039/c8np00069gopenalex-snapshot
Isolation of naturally occurring novel isoflavonoids: an update
inferred← citeshttps://doi.org/10.1039/c9ra07198aopenalex-snapshot
A bio-inspired synthesis of hybrid flavonoids from 2-hydroxychalcone driven by visible light
inferred← citeshttps://doi.org/10.1039/d0cb00218fopenalex-snapshot
Brief survey on organometalated antibacterial drugs and metal-based materials with antibacterial activity
inferred← citeshttps://doi.org/10.1039/d1gc04479fopenalex-snapshot
Sustainable electrochemical dehydrogenative C(sp 3 )–H mono/di-alkylations
inferred← citeshttps://doi.org/10.1039/d4np00060aopenalex-snapshot
Total synthesis of isoflavonoids
inferred← citeshttps://doi.org/10.1039/d5np00054hopenalex-snapshot
Rotenoid diversity, distribution and evolution in plant lineages
inferred← citeshttps://doi.org/10.1051/e3sconf/20186703003openalex-snapshot
Effect of mother-in-law’s tongue leaves (Sansevieria trifasciata) extract’s solvent polarity on anti-diabetic activity through in vitro α-glucosidase enzyme inhibition test
inferred← citeshttps://doi.org/10.1055/a-2501-4796openalex-snapshot
A Revised Protecting Group Strategy Enables a Divergent Synthesis of Prenylated Isoflavones from Psoralea corylifolia
inferred← citeshttps://doi.org/10.1055/a-2705-4229openalex-snapshot
Total Synthesis of Vestitol and Medicarpin
inferred← citeshttps://doi.org/10.1055/s-0032-1328300openalex-snapshot
New Concepts, Experimental Approaches, and Dereplication Strategies for the Discovery of Novel Phytoestrogens from Natural Sources
inferred← citeshttps://doi.org/10.1055/s-0037-1610669openalex-snapshot
Palladium-Catalyzed Coupling Reactions on Functionalized 2-Trifluoromethyl-4-chromenone Scaffolds: Synthesis of Highly Functionalized Trifluoromethyl Heterocycles
inferred← citeshttps://doi.org/10.1063/1.4973148openalex-snapshot
Phytochemical analysis and antioxidant capacity of Lycopodium clavatum Linn. from Lake Sebu, South Cotabato, Philippines
inferred← citeshttps://doi.org/10.1071/fp15204openalex-snapshot
Hydrogen-rich water-alleviated ultraviolet-B-triggered oxidative damage is partially associated with the manipulation of the metabolism of (iso)flavonoids and antioxidant defence in Medicago sativa
inferred← citeshttps://doi.org/10.1080/00397911.2012.661910openalex-snapshot
6-Endo Heck Cyclization of 3-(2-Iodophenoxy)methylbenzofurans: A Useful Approach to Pterocarpenes
inferred← citeshttps://doi.org/10.1080/10286020.2020.1845162openalex-snapshot
Three new monocyclic monoterpenoid O-glycosides from the roots of Glycyrrhiza uralensis
inferred← citeshttps://doi.org/10.1080/10286020802217598openalex-snapshot
Two new isoflavanones from Erythrina costaricensis
inferred← citeshttps://doi.org/10.1080/10408398.2015.1045968openalex-snapshot
Dietary Isoflavones as Modulators of Drug Metabolizing Enzymes and Transporters: Effect on Prescription Medicines
inferred← citeshttps://doi.org/10.1080/10715762.2023.2170880openalex-snapshot
Guaiacol oxidation: theoretical insight into thermochemistry of radical processes involving methoxy group demethylation
inferred← citeshttps://doi.org/10.1080/10717544.2021.1979126openalex-snapshot
Gelatin hydrogel/contact lens composites as rutin delivery systems for promoting corneal wound healing
inferred← citeshttps://doi.org/10.1080/10826076.2016.1147461openalex-snapshot
Characterization of polyphenols in Agastache rugosa leaves and inflorescences by UPLC–qTOF–MS following FCPC separation
inferred← citeshttps://doi.org/10.1080/11263504.2018.1478906openalex-snapshot
Metabolic profiling of rhizomes of native populations of the strictly endemic Croatian species Iris adriatica
inferred← citeshttps://doi.org/10.1080/13543776.2017.1339791openalex-snapshot
A patent review of the therapeutic potential of isoflavones (2012-2016)
inferred← citeshttps://doi.org/10.1080/13543776.2026.2642104openalex-snapshot
An updated patent review of isoflavones and isocoumarins (2018–2024)
inferred← citeshttps://doi.org/10.1080/14786410802292286openalex-snapshot
Three new isoflavanones fromErythrina costaricensis
inferred← citeshttps://doi.org/10.1080/14786419.2014.1003062openalex-snapshot
The genusMachaerium(Fabaceae): taxonomy, phytochemistry, traditional uses and biological activities
inferred← citeshttps://doi.org/10.1080/14786419.2018.1425858openalex-snapshot
Sesbagrandiflorain A and B: isolation of two new 2-arylbenzofurans from the stem bark ofSesbania grandiflora
inferred← citeshttps://doi.org/10.1080/15226514.2010.495143openalex-snapshot
Hydrocarbon Phytoremediation in the FamilyFabacea—A Review
inferred← citeshttps://doi.org/10.1088/1742-6596/1013/1/012198openalex-snapshot
Cytotoxic activity of erypogein d from erythrina poeppigiana (leguminosae) against cervical cancer (HeLa), breast cancer (MCF-7) and ovarian cancer (SKOV-3) cells
inferred← citeshttps://doi.org/10.1093/jee/toac198openalex-snapshot
Influence of Wireworm Diet on its Susceptibility to and Control With the Entomopathogenic FungusMetarhizium brunneum(Hypocreales: Clavicipitaceae) in Laboratory and Field Settings
inferred← citeshttps://doi.org/10.1093/jxb/erx177openalex-snapshot
Current understanding of the pathways of flavonoid biosynthesis in model and crop plants
inferred← citeshttps://doi.org/10.1093/nar/gkad980openalex-snapshot
RefMetaPlant: a reference metabolome database for plants across five major phyla
inferred← citeshttps://doi.org/10.1093/pcp/pct057openalex-snapshot
Glycyrrhiza uralensis Transcriptome Landscape and Study of Phytochemicals
inferred← citeshttps://doi.org/10.1094/phyto-12-12-0328-ropenalex-snapshot
Glyceollin is an Important Component of Soybean Plant Defense Against Phytophthora sojae and Macrophomina phaseolina
inferred← citeshttps://doi.org/10.1104/pp.108.123679openalex-snapshot
Molecular Cloning and Characterization of a cDNA for Pterocarpan 4-Dimethylallyltransferase Catalyzing the Key Prenylation Step in the Biosynthesis of Glyceollin, a Soybean Phytoalexin
inferred← citeshttps://doi.org/10.1104/pp.109.143966openalex-snapshot
Post-Genomics Studies of Developmental Processes in Legume Seeds
inferred← citeshttps://doi.org/10.1104/pp.17.00586openalex-snapshot
Identification and Characterization of Daurichromenic Acid Synthase Active in Anti-HIV Biosynthesis
inferred← citeshttps://doi.org/10.1104/pp.18.00655openalex-snapshot
An Aromatic Farnesyltransferase Functions in Biosynthesis of the Anti-HIV Meroterpenoid Daurichromenic Acid
inferred← citeshttps://doi.org/10.1107/s2053229617014966openalex-snapshot
Deciphering composition and connectivity of a natural product with the assistance of MS and 2D NMR
inferred← citeshttps://doi.org/10.1111/cbdd.14353openalex-snapshot
Neuroprotective potential of formononetin, a naturally occurring isoflavone phytoestrogen
inferred← citeshttps://doi.org/10.1111/j.1462-2920.2011.02424.xopenalex-snapshot
Virulence quenching with a prenylated isoflavanone renders the Malagasy legume Dalbergia pervillei resistant to Rhodococcus fascians
inferred← citeshttps://doi.org/10.1111/pbi.12118openalex-snapshot
Co‐expression of Arabidopsis transcription factor, At MYB 12, and soybean isoflavone synthase, Gm IFS 1, genes in tobacco leads to enhanced biosynthesis of isoflavones and flavonols resulting in osteoprotective activity
inferred← citeshttps://doi.org/10.1111/pbi.13335openalex-snapshot
Metabolite‐based genome‐wide association study enables dissection of the flavonoid decoration pathway of wheat kernels
inferred← citeshttps://doi.org/10.1111/tpj.14178openalex-snapshot
Multi‐tissue integration of transcriptomic and specialized metabolite profiling provides tools for assessing the common bean (Phaseolus vulgaris) metabolome
inferred← citeshttps://doi.org/10.1134/s1021443717010101openalex-snapshot
Proteomic analysis of isozymes in Butea superba leaves
inferred← citeshttps://doi.org/10.1134/s106235901903004xopenalex-snapshot
Secondary Metabolites of Micromycetes in Plants of the Family Fabaceae, Genera Lathyrus, Vicia
inferred← citeshttps://doi.org/10.1177/1934578x1701200825openalex-snapshot
Prenylated Isoflavanones from the Stem Bark of Erythrina poeppigiana (Leguminosae) and its Antimalarial Properties
inferred← citeshttps://doi.org/10.1186/1476-511x-9-49openalex-snapshot
Anti-obesity effect of an isoflavone fatty acid ester on obese mice induced by high fat diet and its potential mechanism
inferred← citeshttps://doi.org/10.1186/s12864-023-09918-wopenalex-snapshot
Genome-wide identification and expression analysis of the glycosyl hydrolase family 1 genes in Medicago sativa revealed their potential roles in response to multiple abiotic stresses
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