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Oxytropis falcata

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fdc0eebcf4312025659
Scientific name Oxytropis falcata
Authority Bunge
First published in Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7, 22(1): 156 (1874)

Description Top

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Synonyms Top

Scientific name Authority First published in
Oxytropis holdereri Ulbr. Notizbl. Königl. Bot. Gart. Berlin3: 193 (1902)
Oxytropis falcata var. falcata Bunge
Oxytropis hedinii Ulbr. Beibl. Bot. Jahrb. Syst.35: 680 (1905)
Astragalus holdereri (Ulbr.) Kuntze Deutsche Bot. Monatsschr.21: 173 (1903)
Spiesia falcata (Bunge) Kuntze Revis. Gen. Pl.1: 206 (1891)
Oxytropis falcata f. albiflora Y.H.Wu Acta Bot. Boreal.-Occid. Sin.28: 1910 (2008)
Oxytropis falcata var. maquensis C.W.Chang Acta Bot. Boreal.-Occid. Sin.7: 202 (1987)
Oxytropis popovii Vassilcz. Novosti Sist. Vyssh. Rast.6: 152 (1970)

Common names Top

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Language Common/alternative name
Chinese 棘豆
Chinese 莪大夏
Chinese 镰形棘豆
Chinese 镰荚棘豆
Chinese 镰荚棘豆（镰形棘豆）

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000198975
Tropicos 13031070
KEW urn:lsid:ipni.org:names:511449-1
The Plant List ild-45486
Open Tree Of Life 3925864
Observations.org 124876
NCBI Taxonomy 1479707
IUCN Red List 19891895
IPNI 179589-2
iNaturalist 138721
GBIF 5360815
EPPO OXRFA
EOL 680214
Elurikkus 527989
CMAUP NPO2765

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Response of species dominance and niche of plant community to wetland degradation along alpine lake riparian Wu S, Dong S, Wang Z, Li S, Ma C, Li Z Front Plant Sci 25-Mar-2024
PMCID:PMC10999619
doi:10.3389/fpls.2024.1352834
PMID:38590743
Traditional Tibetan medicine: therapeutic potential in lung diseases Li C, Li Y, Huang X, Li S, Sangji K, Gu R Front Pharmacol 18-Mar-2024
PMCID:PMC10986185
doi:10.3389/fphar.2024.1365911
PMID:38567353
Meeting abstracts from botanical symposium 2022: exploring innovative approaches in Chinese medicines—from bench to bedside N/A Chin Med 01-Sep-2023
PMCID:PMC10472541
doi:10.1186/s13020-023-00796-8
PMID:37658405
From In Silico Simulation between TGF-β Receptors and Quercetin to Clinical Insight of a Medical Device Containing Allium cepa: Its Efficacy and Tolerability on Post-Surgical Scars Cosio T, Costanza G, Coniglione F, Romeo A, Iacovelli F, Diluvio L, Dika E, Shumak RG, Rossi P, Bianchi L, Falconi M, Campione E Life (Basel) 21-Aug-2023
PMCID:PMC10455185
doi:10.3390/life13081781
PMID:37629638
A systematic review of the research progress of traditional Chinese medicine against pulmonary fibrosis: from a pharmacological perspective Qin S, Tan P, Xie J, Zhou Y, Zhao J Chin Med 03-Aug-2023
PMCID:PMC10398979
doi:10.1186/s13020-023-00797-7
PMID:37537605
A Review of Classification, Biosynthesis, Biological Activities and Potential Applications of Flavonoids Chen S, Wang X, Cheng Y, Gao H, Chen X Molecules 25-Jun-2023
PMCID:PMC10343696
doi:10.3390/molecules28134982
PMID:37446644
Editorial: Actinobacteria plant interaction: recent molecular tools and biology Wang Z, Kumar A, Singh P, Solanki MK Front Microbiol 10-May-2023
PMCID:PMC10206216
doi:10.3389/fmicb.2023.1209699
PMID:37234536
Effects of natural products on skin inflammation caused by abnormal hormones secreted by the adrenal gland Xie W, Zhang C, Wang T, Wang J, Fu F Front Pharmacol 03-May-2023
PMCID:PMC10188947
doi:10.3389/fphar.2023.1156271
PMID:37205913
Pangenome analysis of the genus Herbiconiux and proposal of four new species associated with Chinese medicinal plants Deng Y, Jiang ZM, Han XF, Su J, Yu LY, Liu WH, Zhang YQ Front Microbiol 28-Feb-2023
PMCID:PMC10011130
doi:10.3389/fmicb.2023.1119226
PMID:36925467
Traditional Tibetan medicine to fight against COVID-19: Basic theory and therapeutic drugs Zhang K, Wang L, Peng J, Sangji K, Luo Y, Zeng Y, Zeweng Y, Fan G Front Pharmacol 16-Feb-2023
PMCID:PMC9978713
doi:10.3389/fphar.2023.1098253
PMID:36874035
Flavonoid Components, Distribution, and Biological Activities in Taxus: A review Wei Q, Li QZ, Wang RL Molecules 10-Feb-2023
PMCID:PMC9959731
doi:10.3390/molecules28041713
PMID:36838700
Wound healing properties of a new formulated flavonoid-rich fraction from Dodonaea viscosa Jacq. leaves extract Subramanian S, Duraipandian C, Alsayari A, Ramachawolran G, Wong LS, Sekar M, Gan SH, Subramaniyan V, Seethalakshmi S, Jeyabalan S, Dhanasekaran S, Chinni SV, Mat Rani NN, Wahab S Front Pharmacol 02-Feb-2023
PMCID:PMC9932054
doi:10.3389/fphar.2023.1096905
PMID:36817128
Variation characteristics of different plant functional groups in alpine desert steppe of the Altun Mountains, northern Qinghai-Tibet Plateau Zhang A, Li X, Zeng F, Jiang Y, Wang R Front Plant Sci 13-Sep-2022
PMCID:PMC9513480
doi:10.3389/fpls.2022.961692
PMID:36176676
A Comprehensive Review of Natural Compounds for Wound Healing: Targeting Bioactivity Perspective Trinh XT, Long NV, Van Anh LT, Nga PT, Giang NN, Chien PN, Nam SY, Heo CY Int J Mol Sci 24-Aug-2022
PMCID:PMC9455684
doi:10.3390/ijms23179573
PMID:36076971
7-Hydroxyflavone Alleviates Myocardial Ischemia/Reperfusion Injury in Rats by Regulating Inflammation Zhang Q, Peng Y, Liu J, Yang Y, Hu Z, Zhou Y, Ma J, Zhang D Molecules 23-Aug-2022
PMCID:PMC9458087
doi:10.3390/molecules27175371
PMID:36080137

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Acetophenones
(5-Acetyl-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-3-yl) 4-acetyloxy-2-methylbut-2-enoate 163009733 Click to see CC(=C)C1C(C2=C(O1)C=CC(=C2)C(=O)C)OC(=O)C(=CCOC(=O)C)C 358.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.010
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives
N-Formyl-4-hydroxybenzamide 71370414 Click to see C1=CC(=CC=C1C(=O)NC=O)O 165.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.010
N-Formylbenzamide 151196 Click to see C1=CC=C(C=C1)C(=O)NC=O 149.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.010
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
4-Hydroxybenzamide 65052 Click to see C1=CC(=CC=C1C(=O)N)O 137.14 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.010
N-[(S)-2-Hydroxy-2-phenylethyl]benzamide 6542363 Click to see C1=CC=C(C=C1)C(CNC(=O)C2=CC=CC=C2)O 241.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.010
> Lignans, neolignans and related compounds / Cyclobutane lignans
(3beta,4alpha-Diphenylcyclobutane-1beta,2alpha-diyl)bis[(2,4-dihydroxyphenyl)methanone] 102228233 Click to see C1=CC=C(C=C1)C2C(C(C2C(=O)C3=C(C=C(C=C3)O)O)C(=O)C4=C(C=C(C=C4)O)O)C5=CC=CC=C5 480.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-ene-11,22-diol 44253988 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6O)C)C)C)C)(C)CO)O 472.70 unknown https://doi.org/10.1021/NP900199X
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-22-methoxy-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-ol 44253989 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6OC)C)C)C)C)(C)CO)O 486.70 unknown https://doi.org/10.1021/NP900199X
(1R,2R,5S,6R,9R,10S,11S,14S,15R,19S,21R,22R)-10-(hydroxymethyl)-22-methoxy-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-ol 163008794 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6OC)C)C)C)C)(C)CO)O 486.70 unknown https://doi.org/10.1021/NP900199X
(2R,4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid 21594159 Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)(C)C(=O)O 472.70 unknown https://doi.org/10.1021/NP900199X
(3S,4S,4aR,6aR,6bS,8aR,9R,11R,12aS,14aR,14bR)-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol 14335966 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(CC5O)(C)CO)C)C)C)(C)CO)O 474.70 unknown https://doi.org/10.1021/NP900199X
(4aS,6bR,9S,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,2,4a,6a,6b,9,12a-heptamethyl-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picen-3-one 5321410 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C)C)C)(C)CO)O)C)C 456.70 unknown https://doi.org/10.1021/NP900199X
(4R,4aS,6aS,6bR,8aS,12aR,14aS,14bS)-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,4a,5,6,7,8,10,12,12a,14,14a-dodecahydropicene-3,9-dione 133561860 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)C)C 454.70 unknown https://doi.org/10.1021/NP900199X
10-(Hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-ene-11,22-diol 74975619 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6O)C)C)C)C)(C)CO)O 472.70 unknown https://doi.org/10.1021/NP900199X
10-(Hydroxymethyl)-22-methoxy-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-ol 74975620 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6OC)C)C)C)C)(C)CO)O 486.70 unknown https://doi.org/10.1021/NP900199X
11-Hydroxy-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-22-one 162948673 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C)C)(C)CO)O 470.70 unknown https://doi.org/10.1021/NP900199X
24-Hydroxy-beta-amyrin 14167253 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C)C 442.70 unknown https://doi.org/10.1021/NP900199X
3-Oxoazukisapogenol 44253990 Click to see CC12CCC(CC1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)CO)C)(C)C(=O)O 470.70 unknown https://doi.org/10.1021/NP900199X
3,24-Dihydroxy-12-oleanen-22-one 13632870 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)O)C)C 456.70 unknown https://doi.org/10.1021/NP900199X
3beta,22beta,24-Trihydroxyoleana-12-ene-30-oic acid gamma-lactone 102482971 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C)C)(C)CO)O 470.70 unknown https://doi.org/10.1021/NP900199X
4-(Hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 14167252 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C)C 442.70 unknown https://doi.org/10.1021/NP900199X
4-(Hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,4a,5,6,7,8,10,12,12a,14,14a-dodecahydropicene-3,9-dione 124222318 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)C)C 454.70 unknown https://doi.org/10.1021/NP900199X
4,11-Bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol 5315488 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(CC5O)(C)CO)C)C)C)(C)CO)O 474.70 unknown https://doi.org/10.1021/NP900199X
9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-2-carboxylic acid 74975621 Click to see CC12CCC(CC1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)CO)C)(C)C(=O)O 470.70 unknown https://doi.org/10.1021/NP900199X
9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 85182077 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)C)C 456.70 unknown https://doi.org/10.1021/NP900199X
Abrisapogenol E 14335968 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(CC5O)(C)CO)C)C)C)(C)CO)O 474.70 unknown https://doi.org/10.1021/NP900199X
Azukisapogenol 73744576 Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)(C)C(=O)O 472.70 unknown https://doi.org/10.1021/NP900199X
CID 429190 429190 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C 458.70 unknown https://doi.org/10.1021/NP900199X
Melilotigenin B 91895471 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)C)C 454.70 unknown https://doi.org/10.1021/NP900199X
Melilotigenin C 10551785 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)C)C 456.70 unknown https://doi.org/10.1021/NP900199X
Soyasapogenol B 115012 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C 458.70 unknown https://doi.org/10.1021/NP900199X
Soyasapogenol E 13632872 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)O)C)C 456.70 unknown https://doi.org/10.1021/NP900199X
> Organoheterocyclic compounds / Benzopyrans
4a-hydroxy-3-(2-hydroxy-3,4-dimethoxyphenyl)-3,4,5,6-tetrahydro-2H-chromen-7-one 75254139 Click to see COC1=C(C(=C(C=C1)C2CC3(CCC(=O)C=C3OC2)O)O)OC 320.30 unknown https://doi.org/10.1021/NP100339U
Oxytropisoflavan B 46918734 Click to see COC1=C(C(=C(C=C1)C2CC3(CCC(=O)C=C3OC2)O)O)OC 320.30 unknown https://doi.org/10.1021/NP100339U
> Organoheterocyclic compounds / Indoles and derivatives / Benzoylindoles
Oxytrofalcatin A 46850030 Click to see C1=CC=C(C=C1)C(=O)N2C=C(C3=CC=CC=C32)O 237.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.010
Oxytrofalcatin B 46850031 Click to see C1=CC=C2C(=C1)C(=CN2C(=O)C3=CC=C(C=C3)O)O 253.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.010
Oxytrofalcatin C 46850032 Click to see COC1=CN(C2=CC=CC=C21)C(=O)C3=CC=C(C=C3)O 267.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.010
Oxytrofalcatin D 46850205 Click to see COC1=CN(C2=C1C(=CC=C2)O)C(=O)C3=CC=C(C=C3)O 283.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.010
Oxytrofalcatin E 46850206 Click to see CC(=CCC1=C(C=CC(=C1)C(=O)N2C=C(C3=CC=CC=C32)O)O)C 321.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.010
Oxytrofalcatin F 46850207 Click to see C1=CC=C2C(=C1)C(=CN2C(=O)C3=CC(=CC=C3)O)O 253.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.010
> Organoheterocyclic compounds / Tetrahydrofurans
(3S)-3-methyl-5-[(1R,2S,4S)-1,3,3-trimethyl-7-oxabicyclo[2.2.1]heptan-2-yl]pent-1-en-3-ol 162992138 Click to see CC1(C2CCC(C1CCC(C)(C=C)O)(O2)C)C 238.37 unknown https://doi.org/10.1021/NP900199X
3-Methyl-5-(1,3,3-trimethyl-7-oxabicyclo[2.2.1]heptan-2-yl)pent-1-en-3-ol 85107207 Click to see CC1(C2CCC(C1CCC(C)(C=C)O)(O2)C)C 238.37 unknown https://doi.org/10.1021/NP900199X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown https://doi.org/10.1021/NP100339U
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)- 1889 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1007/S10600-009-9291-4
https://doi.org/10.1021/NP100339U
5,7-Dihydroxyflavanone 238782 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1007/S10600-009-9291-4
7-Hydroxyflavanone 1890 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown https://doi.org/10.1021/NP100339U
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1007/S10600-009-9291-4
https://doi.org/10.1021/NP100339U
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1007/S10600-009-9291-4
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1007/S10600-009-9291-4
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown https://doi.org/10.1007/S10600-009-9291-4
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/S10600-009-9291-4
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1007/S10600-009-9291-4
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/S10600-009-9291-4
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1007/S10600-009-9291-4
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1007/S10600-009-9291-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5R,6R)-4,5-Dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 10919701 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 60200223 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)O)O)O)O 608.50 unknown https://doi.org/10.1021/NP300292F
3-[(2S,5R,6R)-4,5-dihydroxy-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 44391816 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1021/NP300292F
3-[6-O-(3-O-beta-D-Xylopyranosyl-alpha-L-rhamnopyranosyl)-beta-D-galactopyranosyloxy]-4',5,7-trihydroxyflavone 21668680 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)OC6C(C(C(CO6)O)O)O)O 726.60 unknown via CMAUP database
4',5,7-Trihydroxy-3-[2-O-alpha-L-rhamnopyranosyl-6-O-(3-O-beta-D-xylopyranosyl-alpha-L-rhamnopyranosyl)-beta-D-galactopyranosyloxy]flavone 10865825 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)COC6C(C(C(C(O6)C)O)OC7C(C(C(CO7)O)O)O)O)O)O)O)O)O 872.80 unknown via CMAUP database
Biorobin 15944778 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/NP300292F
Oxytroflavoside A 60200065 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)COC(=O)CC(C)(CC(=O)O)O)O)O)O)O)O 752.70 unknown https://doi.org/10.1021/NP300292F
Oxytroflavoside B 60200066 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)OC(=O)CC(C)(CC(=O)O)O)O)O)O 752.70 unknown https://doi.org/10.1021/NP300292F
Oxytroflavoside C 60200220 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)OC(=O)CC(C)(CC(=O)O)O)O)O)O)O 752.70 unknown https://doi.org/10.1021/NP300292F
Oxytroflavoside D 60200221 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC)C4=CC=C(C=C4)O)O)O)O)O 606.50 unknown https://doi.org/10.1021/NP300292F
Oxytroflavoside E 60200222 Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC)C4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 768.70 unknown https://doi.org/10.1021/NP300292F
Oxytroflavoside G 60200370 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 754.70 unknown https://doi.org/10.1021/NP300292F
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 3-O-[alpha-L-rhamnopyranosyl(1->2)-beta-D-galactopyranosyl]-7-O-alpha-L-rhamnopyranoside 57397583 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)CO)O)O)O)O)O 740.70 unknown via CMAUP database
Kaempferol 3-rutinoside 7-rhamnoside 21676297 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1021/NP300292F
Robinin 5281693 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1021/NP300292F
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-7-Methoxyflavanone 688883 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=CC=C3 254.28 unknown https://doi.org/10.1021/NP100339U
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxychroman-4-one 348130 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1021/NP100339U
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1007/S10600-009-9291-4
https://doi.org/10.1021/NP100339U
5-Hydroxy-7-methoxyflavanone 4101463 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1007/S10600-009-9291-4
https://doi.org/10.1021/NP100339U
7-Methoxyflavanone 2825024 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=CC=C3 254.28 unknown https://doi.org/10.1021/NP100339U
Liquiritigenin 7-methylether 14157884 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=C(C=C3)O 270.28 unknown https://doi.org/10.1021/NP100339U
Methyl-liquiritigenin 10265122 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=C(C=C3)O 270.28 unknown https://doi.org/10.1021/NP100339U
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1021/NP100339U
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one 26088035 Click to see C1C(C(=O)C2=C(O1)C=C(C=C2)O)CC3=CC=C(C=C3)O 270.28 unknown https://doi.org/10.1021/NP100339U
7,4'-Dihydroxyhomoisoflavanone 3759709 Click to see C1C(C(=O)C2=C(O1)C=C(C=C2)O)CC3=CC=C(C=C3)O 270.28 unknown https://doi.org/10.1021/NP100339U
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(6aR,11aR)-9-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,10-diol 154804627 Click to see COC1=C(C2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O)O 286.28 unknown https://doi.org/10.1021/NP100339U
(6aR)-9,10-Dimethoxy-6aalpha,11aalpha-dihydro-6H-benzofuro[3,2-c][1]benzopyran-3,8-diol 46918735 Click to see COC1=C(C=C2C3COC4=C(C3OC2=C1OC)C=CC(=C4)O)O 316.30 unknown https://doi.org/10.1021/NP100339U
(l)-Edunol 182148 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=CC5=C(C=C34)OCO5)C 352.40 unknown https://doi.org/10.1021/NP100339U
3-Hydroxy-8,9-methylenedioxy-2-prenylpterocarpan 494278 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=CC5=C(C=C34)OCO5)C 352.40 unknown https://doi.org/10.1021/NP100339U
3-Hydroxy-8,9-methylenedioxypterocarpane 363863 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown https://doi.org/10.1021/NP100339U
9,10-dimethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,8-diol 46919617 Click to see COC1=C(C=C2C3COC4=C(C3OC2=C1OC)C=CC(=C4)O)O 316.30 unknown https://doi.org/10.1021/NP100339U
Maackiain 91510 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown https://doi.org/10.1021/NP100339U
Vesticarpan 44257448 Click to see COC1=C(C2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O)O 286.28 unknown https://doi.org/10.1021/NP100339U
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein 5281708 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 254.24 unknown https://doi.org/10.1021/NP100339U
Pseudobaptigenin 5281805 Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O 282.25 unknown https://doi.org/10.1021/NP100339U
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavanquinones
5-[(3R)-7-hydroxy-3,4-dihydro-2H-chromen-3-yl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione 10403457 Click to see COC1=C(C(=O)C(=CC1=O)C2CC3=C(C=C(C=C3)O)OC2)OC 316.30 unknown https://doi.org/10.1021/NP100339U
Pendulone 5320464 Click to see COC1=C(C(=O)C(=CC1=O)C2CC3=C(C=C(C=C3)O)OC2)OC 316.30 unknown https://doi.org/10.1021/NP100339U
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
5,7-dihydroxy-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxyphenyl]chromen-4-one;Sophoricoside 6078194 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown https://doi.org/10.1021/NP100339U
7-Hydroxy-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 23815384 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown https://doi.org/10.1021/NP100339U
Daidzein-4'-glucoside 49862229 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown https://doi.org/10.1021/NP100339U
Sophoricoside 5321398 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown https://doi.org/10.1021/NP100339U
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 2-O-methylated isoflavonoids
(3R)-3-(6-methoxy-1,3-benzodioxol-5-yl)-3,4-dihydro-2H-chromen-7-ol 163092609 Click to see COC1=CC2=C(C=C1C3CC4=C(C=C(C=C4)O)OC3)OCO2 300.30 unknown https://doi.org/10.1021/NP100339U
Astraciceran 156986 Click to see COC1=CC2=C(C=C1C3CC4=C(C=C(C=C4)O)OC3)OCO2 300.30 unknown https://doi.org/10.1021/NP100339U
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-Methoxydaidzein 5319422 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown https://doi.org/10.1021/NP100339U
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(R)-Isomucronulatol 10380176 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)OC 302.32 unknown https://doi.org/10.1021/NP100339U
4-[(1R,2R)-2-hydroxy-1-[(3R)-7-hydroxy-3-(2-hydroxy-3,4-dimethoxyphenyl)-3,4-dihydro-2H-chromen-6-yl]-3-(4-hydroxyphenyl)propyl]benzene-1,3-diol 162916051 Click to see COC1=C(C(=C(C=C1)C2CC3=CC(=C(C=C3OC2)O)C(C4=C(C=C(C=C4)O)O)C(CC5=CC=C(C=C5)O)O)O)OC 560.60 unknown https://doi.org/10.1021/NP100339U
4-[2-hydroxy-1-[7-hydroxy-3-(2-hydroxy-3,4-dimethoxyphenyl)-3,4-dihydro-2H-chromen-6-yl]-3-(4-hydroxyphenyl)propyl]benzene-1,3-diol 75254138 Click to see COC1=C(C(=C(C=C1)C2CC3=CC(=C(C=C3OC2)O)C(C4=C(C=C(C=C4)O)O)C(CC5=CC=C(C=C5)O)O)O)OC 560.60 unknown https://doi.org/10.1021/NP100339U
Isomucronulatol 602152 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)OC 302.32 unknown https://doi.org/10.1021/NP100339U
Oxytropisoflavan A 46918733 Click to see COC1=C(C(=C(C=C1)C2CC3=CC(=C(C=C3OC2)O)C(C4=C(C=C(C=C4)O)O)C(CC5=CC=C(C=C5)O)O)O)OC 560.60 unknown https://doi.org/10.1021/NP100339U
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
(3R)-3-(2,3-Dihydroxy-4-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-ol 15939757 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)O 288.29 unknown https://doi.org/10.1021/NP100339U
2H-1-Benzopyran-7-ol, 3,4-dihydro-3-(3-hydroxy-2,4-dimethoxyphenyl)-, (3R)- 13873811 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)OC)O 302.32 unknown https://doi.org/10.1021/NP100339U
7,5',6'-Trihydroxy-4'-methoxyisoflavan 5326316 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)O 288.29 unknown https://doi.org/10.1021/NP100339U
Calycosin 5280448 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown https://doi.org/10.1021/NP100339U
Mucronulatol 4484949 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)OC)O 302.32 unknown https://doi.org/10.1021/NP100339U
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxybiochanin A 5282075 Click to see COC1=CC(=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown https://doi.org/10.1021/NP100339U
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1021/NP100339U
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Isoformononetin 3764 Click to see COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O 268.26 unknown https://doi.org/10.1021/NP100339U
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',4'-Dihydroxydihydrochalcone 586491 Click to see C1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2)O)O 242.27 unknown https://doi.org/10.1021/NP100339U
https://doi.org/10.1007/S10600-009-9291-4
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2-Hydroxy-4-methoxyphenyl)-3-phenylprop-2-en-1-one 265720 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=CC=C2)O 254.28 unknown https://doi.org/10.1021/NP100339U
https://doi.org/10.1007/S10600-009-9291-4
2-Propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)- 592216 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O 270.28 unknown https://doi.org/10.1021/NP100339U
2-Propen-1-one, 1-(2,4-dihydroxyphenyl)-3-phenyl- 344530 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown https://doi.org/10.1007/S10600-009-9291-4
https://doi.org/10.1021/NP100339U
2'-Hydroxy-4'-Methoxychalcone 5380645 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=CC=C2)O 254.28 unknown https://doi.org/10.1021/NP100339U
https://doi.org/10.1007/S10600-009-9291-4
2',4'-Dihydroxychalcone 5376979 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown https://doi.org/10.1007/S10600-009-9291-4
https://doi.org/10.1021/NP300292F
https://doi.org/10.1021/NP100339U
4,2'-Dihydroxy-4'-methoxychalcone 6537040 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O 270.28 unknown https://doi.org/10.1021/NP100339U
Chalcone, 2',4'-dihydroxy-4-methoxy- 166795 Click to see COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 270.28 unknown via CMAUP database
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1007/S10600-009-9291-4
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1007/S10600-009-9291-4
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
1-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 193568 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C 324.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
1-(4-Hydroxy-2-methoxyphenyl)-3-phenylprop-2-en-1-one 71442332 Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=CC=C2 254.28 unknown https://doi.org/10.1007/S10600-009-9291-4
4-[(2R)-2-hydroxy-3-(4-hydroxyphenyl)propyl]benzene-1,3-diol 162986392 Click to see C1=CC(=CC=C1CC(CC2=C(C=C(C=C2)O)O)O)O 260.28 unknown https://doi.org/10.1021/NP100339U
4-[2-Hydroxy-3-(4-hydroxyphenyl)propyl]benzene-1,3-diol 21722173 Click to see C1=CC(=CC=C1CC(CC2=C(C=C(C=C2)O)O)O)O 260.28 unknown https://doi.org/10.1021/NP100339U
4'-Hydroxy-2'-methoxychalcone 13842401 Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=CC=C2 254.28 unknown https://doi.org/10.1007/S10600-009-9291-4

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