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Carbon-13 chemical shift assignments of chromones and isoflavones
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112577zenodo-depositor-declared
A previously undescribed phenylethanoid glycoside from Callicarpa kwangtungensis Chun acts as an agonist of the Na/K-ATPase signal transduction pathway
inferred← citeshttps://doi.org/10.1002/cbdv.201400208openalex-snapshot
Free‐Radical‐Scavenging, Antityrosinase, and Cellular Melanogenesis Inhibitory Activities of Synthetic Isoflavones
inferred← citeshttps://doi.org/10.1002/cbdv.202200675openalex-snapshot
First Occurrence of Megastigmane Glucosides in a Plant of Retama Genus
inferred← citeshttps://doi.org/10.1002/hlca.201000210openalex-snapshot
Caragisides A – C, New Isoflavone Glucosides from Caragana conferta with Inhibition of Platelet Aggregation
inferred← citeshttps://doi.org/10.1002/hlca.201600117openalex-snapshot
New Phenolic Compounds from the Roots of Lentil (Lens culinaris)
inferred← citeshttps://doi.org/10.1002/jccs.200400210openalex-snapshot
Flavonoids from the Flowers of Pueraria Lobata
inferred← citeshttps://doi.org/10.1002/jctb.1461openalex-snapshot
Biotransformation of isoflavones by Aspergillus niger as biocatalyst
inferred← citeshttps://doi.org/10.1002/jlac.198519851215openalex-snapshot
Haplopappin, ein 8‐(α‐Methylbenzyl)flavonoid aus Haplopapus foliosus
inferred← citeshttps://doi.org/10.1002/mrc.1260240308openalex-snapshot
Carbon‐13 nuclear magnetic resonance spectra of isoflavones
inferred← citeshttps://doi.org/10.1002/mrc.1260240806openalex-snapshot
1H and 13C chemical shift assignments of homoisoflavanones
inferred← citeshttps://doi.org/10.1002/mrc.1260260306openalex-snapshot
Carbon‐13 nuclear magnetic resonance spectra of brominated catechin derivatives: Stereoelectronic effects on chemical shifts
inferred← citeshttps://doi.org/10.1002/mrc.1270220314openalex-snapshot
Carbon‐13 NMR spectra of isocoumarin, N‐methyl‐1(2H)‐isoquinolinone and related compounds
inferred← citeshttps://doi.org/10.1007/978-1-4899-2915-0_2openalex-snapshot
Carbon-13 NMR Spectroscopy of Flavonoids
inferred← citeshttps://doi.org/10.1007/bf00799170openalex-snapshot
Naphthopyrones, Part I Proton magnetic resonance spectral studies of some methylnaphthopyran-2-one and methylnaphthopyran-4-one derivatives
inferred← citeshttps://doi.org/10.1007/bf01120970openalex-snapshot
Naphthopyrones, part II Carbon-13 magnetic resonance spectral studies of some methylnaphthopyran-2-one and methylnaphthopyran-4-one derivatives
inferred← citeshttps://doi.org/10.1007/s10068-020-00815-6openalex-snapshot
A brief history and spectroscopic analysis of soy isoflavones
inferred← citeshttps://doi.org/10.1007/s10600-014-0891-2openalex-snapshot
Secondary Metabolites of Endophytic Fungus Trichoderma sp. YM 311505 of Azadirachta indica
inferred← citeshttps://doi.org/10.1007/s10600-016-1661-0openalex-snapshot
Novel Isoflavone from the Cockroach Periplaneta americana
inferred← citeshttps://doi.org/10.1016/0009-2797(92)90109-xopenalex-snapshot
Effects of synthetic and naturally occurring flavonoids on metabolic activation of benzo[a]pyrene in hamster embryo cell cultures
inferred← citeshttps://doi.org/10.1016/0031-9422(83)80045-4openalex-snapshot
Three isoflavonoids from Iris germanica
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00636-2openalex-snapshot
Two isoflavones from the bark of Petalostemon purpureus
inferred← citeshttps://doi.org/10.1016/0031-9422(95)00743-1openalex-snapshot
Two isoflavones from the bark of Petalostemon purpureus
inferred← citeshttps://doi.org/10.1016/0960-0760(91)90100-jopenalex-snapshot
The estrogenic activity of certain phytoestrogens in the siberian sturgeon Acipenser baeri
inferred← citeshttps://doi.org/10.1016/b978-0-12-819210-8.00002-3openalex-snapshot
Six-Membered Heterocycles
inferred← citeshttps://doi.org/10.1016/b978-0-444-87449-8.50008-0openalex-snapshot
Methods of Signal Assignment
inferred← citeshttps://doi.org/10.1016/b978-008096519-2.00044-8openalex-snapshot
Pyrans and Fused Pyrans: (i) Structure
inferred← citeshttps://doi.org/10.1016/j.bjp.2015.12.004openalex-snapshot
Isoflavone-aglycone fraction from Glycine max: a promising raw material for isoflavone-based pharmaceutical or nutraceutical products
inferred← citeshttps://doi.org/10.1016/j.bmcl.2003.11.074openalex-snapshot
Anti-inflammatory flavonoids and pterocarpanoid from Crotalaria pallida and C. assamica
inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.08.084openalex-snapshot
Isoflavones with unusually modified B-rings and their evaluation as antiproliferative agents
inferred← citeshttps://doi.org/10.1016/j.carbpol.2013.06.062openalex-snapshot
Multiple complexation of cyclodextrin with soy isoflavones present in an enriched fraction
inferred← citeshttps://doi.org/10.1016/j.fitote.2014.02.010openalex-snapshot
Natural phosphodiesterase-4 (PDE4) inhibitors from Crotalaria ferruginea
inferred← citeshttps://doi.org/10.1016/j.molcatb.2003.09.008openalex-snapshot
Biotransformation of isoflavones by Aspergillus niger, as biocatalyst
inferred← citeshttps://doi.org/10.1016/j.molstruc.2009.12.033openalex-snapshot
Synthesis and structural study on heterocyclic compounds 7-decanoyloxy-3-(4′-substitutedphenyl)-4H-1-benzopyran-4-ones: Crystal structure of 7-decanoyloxy-3-(4′-methylphenyl)-4H-1-benzopyran-4-one
inferred← citeshttps://doi.org/10.1016/j.phytochem.2005.03.013openalex-snapshot
Metabolism of daidzein by Nocardia species NRRL 5646 and Mortierella isabellina ATCC 38063
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.06.003openalex-snapshot
Antigenotoxic prenylated flavonoids from stem bark of Erythrina latissima
inferred← citeshttps://doi.org/10.1016/s0031-9422(00)80573-7openalex-snapshot
Isoflavones of Iris spuria
inferred← citeshttps://doi.org/10.1016/s0031-9422(00)89823-4openalex-snapshot
Isoflavones from Garcinia nervosa
inferred← citeshttps://doi.org/10.1016/s0031-9422(96)00560-2openalex-snapshot
A C-methylflavone from Trianthema portulacastrum
inferred← citeshttps://doi.org/10.1016/s0031-9422(98)00624-4openalex-snapshot
Isoflavone glycosides from Centrosema pubescens
inferred← citeshttps://doi.org/10.1016/s0031-9422(99)00459-8openalex-snapshot
Odoratin 7-O-β-D-glucopyranoside from Bowdichia virgilioides
inferred← citeshttps://doi.org/10.1016/s0040-4020(98)01153-3openalex-snapshot
Synthesis of isoflavonoid deuterium labeled polyphenolic phytoestrogens
inferred← citeshttps://doi.org/10.1016/s0305-1978(99)00064-2openalex-snapshot
Flavonoids from Ficus pumila
inferred← citeshttps://doi.org/10.1016/s0367-326x(99)00084-2openalex-snapshot
Constituents from the roots of Bowdichia virgilioides
inferred← citeshttps://doi.org/10.1021/acs.jafc.6b01094openalex-snapshot
Effect of Soy Sauce on Serum Uric Acid Levels in Hyperuricemic Rats and Identification of Flazin as a Potent Xanthine Oxidase Inhibitor
inferred← citeshttps://doi.org/10.1021/ct050063dopenalex-snapshot
Intrinsic Carbon−Carbon Bond Reactivity at the Manganese Center of Oxalate Decarboxylase from Density Functional Theory
inferred← citeshttps://doi.org/10.1021/ic035450hopenalex-snapshot
Role of Solvation in the Reduction of the Uranyl Dication by Water: A Density Functional Study
inferred← citeshttps://doi.org/10.1021/ja0603453openalex-snapshot
C7and C9Carbon-Rich Bridges in Diruthenium Systems: Synthesis, Spectroscopic, and Theoretical Investigations of Different Oxidation States
inferred← citeshttps://doi.org/10.1021/ja068542popenalex-snapshot
Comparative Reactivity of TpRu(L)(NCMe)Ph (L = CO or PMe3): Impact of Ancillary Ligand L on Activation of Carbon−Hydrogen Bonds Including Catalytic Hydroarylation and Hydrovinylation/Oligomerization of Ethylene
inferred← citeshttps://doi.org/10.1021/ja068999zopenalex-snapshot
Metallaborane Reactivity. A Stoichiometric Mechanism for the Insertion of Two Alkynes into an Iridaborane Framework via a Disposable Molybdenum Chaperone
inferred← citeshttps://doi.org/10.1021/ja073224ropenalex-snapshot
On the Sensitivity of f Electrons to Their Chemical Environment
inferred← citeshttps://doi.org/10.1021/jp061851hopenalex-snapshot
Predicting the Energy of the Water Exchange Reaction and Free Energy of Solvation for the Uranyl Ion in Aqueous Solution
inferred← citeshttps://doi.org/10.1021/la052973oopenalex-snapshot
Modeling Adsorption of the Uranyl Dication on the Hydroxylated α-Al2O3(0001) Surface in an Aqueous Medium. Density Functional Study
inferred← citeshttps://doi.org/10.1021/om020303xopenalex-snapshot
Redox-Switchable Second-Order Molecular Polarizabilities with Electron-Rich Iron σ-Aryl Acetylides
inferred← citeshttps://doi.org/10.1021/om030630kopenalex-snapshot
Electron-Rich Piano-Stool Iron σ-Acetylides. Theoretical and Phenomenological Investigation of Electronic Substituent Effects in Iron(II) Acetylides
inferred← citeshttps://doi.org/10.1021/om0505108openalex-snapshot
Electron-Rich Piano-Stool Iron σ-Acetylides. Electronic Structures of Arylalkynyl Iron(III) Radical Cations
inferred← citeshttps://doi.org/10.1021/om050799topenalex-snapshot
Bonding and Substituent Effects in Electron-Rich Mononuclear Ruthenium σ-Arylacetylides of the Formula [(η2-dppe)(η5-C5Me5)Ru(C⋮C)-1,4-(C6H4)X][PF6]n(n= 0, 1; X = NO2, CN, F, H, OMe, NH2)
inferred← citeshttps://doi.org/10.1021/om060989jopenalex-snapshot
Spin Delocalization in Electron-Rich Iron(III) Piano-Stool σ-Acetylides. An Experimental (NMR) and Theoretical (DFT) Investigation
inferred← citeshttps://doi.org/10.1021/om700673mopenalex-snapshot
Charge Transfer through Isomeric Unsaturated Hydrocarbons. Redox Switchable Optical Properties and Electronic Structure of Substituted Indenes with a Pendant Ferrocenyl
inferred← citeshttps://doi.org/10.1039/p19910003005openalex-snapshot
Expedient synthesis of polyhydroxyisoflavones
inferred← citeshttps://doi.org/10.1039/p19920003015openalex-snapshot
Synthesis of the 5-thiorotenoid system from thiochroman-3-one
inferred← citeshttps://doi.org/10.1080/00150190802063377openalex-snapshot
Synthesis and Phase Behaviour of Some New Isoflavone Derivatives
inferred← citeshttps://doi.org/10.1080/026782999205579openalex-snapshot
Synthesis of new mesogenic compounds having the isoflavone core group
inferred← citeshttps://doi.org/10.1080/1028602021000049104openalex-snapshot
Four new isoflavones from Ampelopsis grossedentata
inferred← citeshttps://doi.org/10.1080/13682820701261892openalex-snapshot
Synthesis and mesomorphic properties of 7‐acyloxy‐3‐(4‐acyloxyphenyl)‐4H‐1‐benzopyran‐4‐one
inferred← citeshttps://doi.org/10.1080/14786419.2024.2302318openalex-snapshot
Extraction, rapid preparation and neuroprotective effect of texasin, a main active constituent from Caragana jubata (Pall.) Poir.
inferred← citeshttps://doi.org/10.1107/s0108270111035761openalex-snapshot
Plumeridoid C from the Amazonian traditional medicinal plantHimatanthus sucuuba
inferred← citeshttps://doi.org/10.1111/j.1744-7909.2006.00227.xopenalex-snapshot
Water‐Soluble Constituents of Cudrania tricuspidata (Carr.) Bur.
inferred← citeshttps://doi.org/10.1248/cpb.53.740openalex-snapshot
Isolation and Structure Determination of Bioactive Isoflavones from Callus Culture of Dipteryx odorata
inferred← citeshttps://doi.org/10.1248/cpb.57.346openalex-snapshot
Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities
inferred← citeshttps://doi.org/10.1271/bbb.62.740openalex-snapshot
Potent Antioxidative Isoflavones Isolated from Soybeans Fermented withAspergillus saitoi
inferred← citeshttps://doi.org/10.1271/bbb.68.1051openalex-snapshot
Isoflavones Found in Korean Soybean Paste as 3-Hydroxy-3-methylglutaryl Coenzyme A Reductase Inhibitors
inferred← citeshttps://doi.org/10.1590/0001-3765201920180204openalex-snapshot
Evaluation of the antimicrobial and antioxidant activity of 7-hydroxy-4’, 6-dimethoxy-isoflavone and essential oil from Myroxylon peruiferum L.f
inferred← citeshttps://doi.org/10.3184/030823408x382135openalex-snapshot
Synthesis of isoflavones via base catalysed condensation reaction of deoxybenzoin
inferred← citeshttps://doi.org/10.3797/scipharm.1112-23openalex-snapshot
A New Isoflavone Glycoside from Dalbergia vacciniifolia (Fabaceae)
inferred← citeshttps://doi.org/10.4028/p-hf5bgaopenalex-snapshot
Phytochemical Characterization of Ochna integerrima roots and their In Vitro Anti-Tyrosinase Property
inferred← citeshttps://doi.org/10.4028/www.scientific.net/amr.550-553.1378openalex-snapshot
Chemical Constituents of Boehmeria macrophylla Hornem
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