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Isoflavonoids of the Leguminosae

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inferredcites →https://doi.org/10.1002/ejoc.200600742openalex-snapshot
Uncommon 5‐Methoxyisoflavans from Desmodium canum
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.884openalex-snapshot
Profiling isoflavone conjugates in root extracts of lupine species with LC/ESI/MSn systems
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/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/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/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/10.1007/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/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/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/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/10.1016/0031-9422(91)80108-dopenalex-snapshot
Two complex flavanones from the roots ofSophora leachiana
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(95)00653-2openalex-snapshot
Antimicrobial isoflavanones from Desmodium canum
inferredcites →https://doi.org/10.1016/0040-4020(61)80016-1openalex-snapshot
Synthetic analogues of wedelolactone
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.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.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.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.2007.04.007openalex-snapshot
A new isoflavone glucoside from Astragalus membranaceus var. mongholicus
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.2007.03.040openalex-snapshot
Crystal Structure of Vestitone 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.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.2007.08.006openalex-snapshot
Isoflavonoids in non-leguminous taxa: A rarity or a rule?
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.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/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/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/s0031-9422(00)00349-6openalex-snapshot
Two isoflavanones from the stem bark of Erythrina sacleuxii
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(02)00035-3openalex-snapshot
Pyrano-isoflavones with erectile-dysfunction activity from Eriosema kraussianum
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(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)00518-9openalex-snapshot
Conrauinones C and D, two isoflavones from stem bark of Millettia conraui
inferredcites →https://doi.org/10.1016/s0031-9422(98)00266-0openalex-snapshot
Purification of 2-Hydroxyisoflavanone Dehydratase from the Cell Cultures of Pueraria Lobata in Honour of Professor G. H. Neil Towers 75TH Birthday
inferredcites →https://doi.org/10.1016/s0031-9422(98)00514-7openalex-snapshot
Biflavonoids and 4,2′-epoxy-3-phenylcoumarins from the moss Mnium hornum
inferredcites →https://doi.org/10.1016/s0065-2113(05)86003-1openalex-snapshot
Metabolic Engineering of Isoflavone Biosynthesis
inferredcites →https://doi.org/10.1021/jf035053popenalex-snapshot
LC/UV/ESI-MS Analysis of Isoflavones in Edamame and Tofu Soybeans
inferredcites →https://doi.org/10.1021/jf0483117openalex-snapshot
Four New Prenylated Isoflavonoids in Tadehagi triquetrum
inferredcites →https://doi.org/10.1021/jf991002+openalex-snapshot
LC-ESI-MS Study of the Flavonoid Glycoside Malonates of Red Clover (Trifolium pratense)
inferredcites →https://doi.org/10.1021/np020425uopenalex-snapshot
Six New Isoflavones and a 5-Deoxyflavonol Glycoside from the Leaves of Ateleia herbert-smithii
inferredcites →https://doi.org/10.1021/np049854dopenalex-snapshot
Cytotoxic Flavonoids from Platymiscium floribundum
inferredcites →https://doi.org/10.1021/np0502037openalex-snapshot
Rapid Extract Dereplication Using HPLC-SPE-NMR: Analysis of Isoflavonoids from Smirnowia iranica
inferredcites →https://doi.org/10.1021/np050233+openalex-snapshot
Coumestans from Hedysarum multijugum
inferredcites →https://doi.org/10.1021/np0502600openalex-snapshot
Isoflavonoids and Other Compounds from Psorothamnus arborescens with Antiprotozoal Activities
inferredcites →https://doi.org/10.1021/np050341wopenalex-snapshot
Isoflavonoids with Antiestrogenic Activity from Millettia pachycarpa
inferredcites →https://doi.org/10.1021/np058057sopenalex-snapshot
Metabolites of the “Smoke Tree”, Dalea spinosa, Potentiate Antibiotic Activity against Multidrug-Resistant Staphylococcus aureus
inferredcites →https://doi.org/10.1021/np058069dopenalex-snapshot
Antibacterial Compounds from Glycyrrhiza u ralensis
inferredcites →https://doi.org/10.1021/np058070copenalex-snapshot
Rautandiols A and B, Pterocarpans and Cytotoxic Constituents from Neorautanenia m itis ,1
inferredcites →https://doi.org/10.1021/np060189dopenalex-snapshot
Phenolic Constituents of the Roots ofSophoraflavescens
inferredcites →https://doi.org/10.1021/np0703904openalex-snapshot
Brandisianins A−F, Isoflavonoids Isolated from Millettia brandisiana in a Screening Program for Death-Receptor Expression Enhancement Activity
inferredcites →https://doi.org/10.1021/np50052a020openalex-snapshot
Traditional Medicinal Plants of Thailand, VIII. Isoflavonoids of Dalbergia candenatensis
inferredcites →https://doi.org/10.1021/np50064a017openalex-snapshot
Plant Antimutagenic Agents, 5. Isolation and Structure of Two New Isoflavones, Fremontin and Fremontone from Psorothamnus fremontii
inferredcites →https://doi.org/10.1021/np50095a005openalex-snapshot
Antitumor Agents, 138. Rotenoids and Isoflavones as Cytotoxic Constituents from Amorpha fruticosa
inferredcites →https://doi.org/10.1021/np970187gopenalex-snapshot
Conrauinones A and B, Two New Isoflavones from Stem Bark of Millettia conraui
inferredcites →https://doi.org/10.1023/b:conc.0000018105.23722.7dopenalex-snapshot
A New Isoflavone fromAstragalus peregrinus
inferredcites →https://doi.org/10.1039/a815241yopenalex-snapshot
Isoflavonoids and related compounds
inferredcites →https://doi.org/10.1039/b416248jopenalex-snapshot
Isoflavonoids in non-leguminous families: an update
inferredcites →https://doi.org/10.1039/b505071popenalex-snapshot
Furanoflavonoids: an overview
inferredcites →https://doi.org/10.1039/b511238aopenalex-snapshot
Isoflavonoids of the Leguminosae
inferredcites →https://doi.org/10.1039/p19880001237openalex-snapshot
Oligomeric isoflavonoids. Part 2. Structure and synthesis of xanthocercin A and B, the first isoflavono-lignoids
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01378.xopenalex-snapshot
Key amino acid residues required for aryl migration catalysed by the cytochrome P450 2‐hydroxyisoflavanone synthase
inferredcites →https://doi.org/10.1055/s-2004-815447openalex-snapshot
Cancer Chemopreventive Activity of Rotenoids fromDerris trifoliata
inferredcites →https://doi.org/10.1055/s-2005-837841openalex-snapshot
New Cytotoxic Prenylated Isoflavonoids fromBituminaria morisiana
inferredcites →https://doi.org/10.1055/s-2005-871297openalex-snapshot
Neuroprotective Flavonoids fromFlemingia macrophylla
inferredcites →https://doi.org/10.1055/s-2005-873200openalex-snapshot
Antiplasmodial Flavonoids fromErythrina sacleuxii
inferredcites →https://doi.org/10.1055/s-2005-916232openalex-snapshot
New Prenylated Metabolites ofDeguelia longeracemosaand Evaluation of their Antimicrobial Potential
inferredcites →https://doi.org/10.1055/s-2005-916252openalex-snapshot
Activity of Isoflavans of Dalea aurea (Fabaceae) against the Opportunistic Ameba Naegleria fowleri
inferredcites →https://doi.org/10.1055/s-2005-916259openalex-snapshot
Induction of Apoptosis by Isoflavonoids from the Leaves ofMillettia taiwanianain Human Leukemia HL-60 Cells
inferredcites →https://doi.org/10.1074/jbc.274.11.7516openalex-snapshot
Evolution of Plant Defense Mechanisms
inferredcites →https://doi.org/10.1074/jbc.m502239200openalex-snapshot
Structural Elucidation of Chalcone Reductase and Implications for Deoxychalcone Biosynthesis
inferredcites →https://doi.org/10.1074/jbc.m605726200openalex-snapshot
An Isoflavone Conjugate-hydrolyzing β-Glucosidase from the Roots of Soybean (Glycine max) Seedlings
inferredcites →https://doi.org/10.1074/jbc.m605767200openalex-snapshot
Mutational Analysis of the Medicago Glycosyltransferase UGT71G1 Reveals Residues That Control Regioselectivity for (Iso)flavonoid Glycosylation
inferredcites →https://doi.org/10.1074/jbc.m702651200openalex-snapshot
A UDP-Glucose:Isoflavone 7-O-Glucosyltransferase from the Roots of Soybean (Glycine max) Seedlings
inferredcites →https://doi.org/10.1080/10286020500289501openalex-snapshot
Two new arylbenzofurans from the roots of Hedysarum multijugum
inferredcites →https://doi.org/10.1080/10286020500289618openalex-snapshot
Studies on the chemical constituents of Psoralea corylifolia L.
inferredcites →https://doi.org/10.1080/10286020500478633openalex-snapshot
Two new isoflavonoids from the roots ofDalbergia congesta(Grah)
inferredcites →https://doi.org/10.1080/10286020600979894openalex-snapshot
New flavonoids and other constituents from Lespedeza cuneata
inferredcites →https://doi.org/10.1080/10575639708043642openalex-snapshot
Isolation and Synthesis of Two New 3-Arylcoumarin Derivatives from the Root of Glycyrrhiza Glabra (Licorice), and Structure Revision of an Antioxidant Isoflavonoid Glabrene
inferredcites →https://doi.org/10.1080/14786410412331272022openalex-snapshot
Isolation and structural elucidation of a novel rotenoid from the seeds ofClitoria fairchildiana
inferredcites →https://doi.org/10.1080/14786410500046513openalex-snapshot
Dalsympathetin – a new isoflavone gentiobioside from Dalbergia sympathetica (Dennst.)
inferredcites →https://doi.org/10.1080/14786410500160942openalex-snapshot
Two new isoflavonoids fromBowdichia virgilioides
inferredcites →https://doi.org/10.1080/14786410500364627openalex-snapshot
Two new isoflavone derivatives from the roots of an Egyptian collection ofLotus polyphyllos
inferredcites →https://doi.org/10.1080/14786410601130091openalex-snapshot
Isolation and characterisation of bioactive isoflavonoids from the roots ofDalbergia horrida
inferredcites →https://doi.org/10.1093/pcp/pcm125openalex-snapshot
2-Hydroxyisoflavanone Dehydratase is a Critical Determinant of Isoflavone Productivity in Hairy Root Cultures of Lotus japonicus
inferredcites →https://doi.org/10.1104/pp.103.025213openalex-snapshot
Characterization of Leachianone G 2″ -Dimethylallyltransferase, a Novel Prenyl Side-Chain Elongation Enzyme for the Formation of the Lavandulyl Group of Sophoraflavanone G in Sophora flavescens Ait. Cell Suspension Cultures
inferredcites →https://doi.org/10.1104/pp.104.056747openalex-snapshot
Molecular and Biochemical Characterization of 2-Hydroxyisoflavanone Dehydratase. Involvement of Carboxylesterase-Like Proteins in Leguminous Isoflavone Biosynthesis
inferredcites →https://doi.org/10.1104/pp.105.062539openalex-snapshot
Metabolic Engineering of Isoflavonoid Biosynthesis in Alfalfa
inferredcites →https://doi.org/10.1105/tpc.105.035055openalex-snapshot
Crystal Structures of a Multifunctional Triterpene/Flavonoid Glycosyltransferase from Medicago truncatula
inferredcites →https://doi.org/10.1105/tpc.106.041376openalex-snapshot
Structural Basis for Dual Functionality of Isoflavonoid O-Methyltransferases in the Evolution of Plant Defense Responses
inferredcites →https://doi.org/10.1107/s1600536805020325openalex-snapshot
7a-O-Methyldeguelol
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02344.xopenalex-snapshot
Genomics‐based selection and functional characterization of triterpene glycosyltransferases from the model legume Medicago truncatula
inferredcites →https://doi.org/10.1139/v07-120openalex-snapshot
Cytotoxic rotenoloids from the stems of Derris trifoliata
inferredcites →https://doi.org/10.1246/bcsj.38.845openalex-snapshot
The Synthesis of Isoelliptol Isoflavone
inferredcites →https://doi.org/10.1246/cl.2007.1382openalex-snapshot
Synthesis of Glaziovianin A: A Potent Antitumor Isoflavone
inferredcites →https://doi.org/10.1248/cpb.53.419openalex-snapshot
Flavonoids from Millettia nitida var. hirsutissima
inferredcites →https://doi.org/10.1248/cpb.53.847openalex-snapshot
The Isolation and Structure Elucidation of Minor Isoflavonoids from Licorice of Glycyrrhiza glabra Origin
inferredcites →https://doi.org/10.1248/cpb.54.1315openalex-snapshot
Puerariafuran, a New Inhibitor of Advanced Glycation End Products (AGEs) Isolated from the Roots of Pueraria lobata
inferredcites →https://doi.org/10.1248/cpb.54.570openalex-snapshot
Four New Isoflavonoids from the Stem Bark of Erythrina variegata
inferredcites →https://doi.org/10.1248/cpb.54.915openalex-snapshot
In Vitro Leishmanicidal Constituents of Millettia pendula
inferredcites →https://doi.org/10.1248/cpb.55.1181openalex-snapshot
Prenylisoflavone Derivatives from the Roots of Hedysarum scoparium
inferredcites →https://doi.org/10.1248/cpb.55.1402openalex-snapshot
.ALPHA.-Glucosidase Inhibitors from Millettia conraui
inferredcites →https://doi.org/10.1271/bbb.70028openalex-snapshot
A Journey of Twenty-Five Years through the Ecological Biochemistry of Flavonoids
inferredcites →https://doi.org/10.1515/znb-2005-0911openalex-snapshot
Isoflavonoids from Seeds of Millettia griffoniana (Bail), 15
inferredcites →https://doi.org/10.1515/znc-1991-5-602openalex-snapshot
Naturally Occurring Coumaranochroman-4-Ones: A New Class Of Isoflavonoids From Lupins And Jamaican Dogwood
inferredcites →https://doi.org/10.3184/030823407x215591openalex-snapshot
Isoflavones from Psorothamnus arborescens via high-throughput Natural Product Chemistry Methods
inferredcites →https://doi.org/10.3987/com-05-10321openalex-snapshot
Two New Isoflavonoids and a New 2-Arylbenzofuran from the Roots of Erythrina variegata
inferredcites →https://doi.org/10.3987/com-05-10350openalex-snapshot
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Isolation and characterization of a cDNA encoding polyketide reductase in Lotus japonicus

What points at this work

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

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