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Dalbergia sissoo

Dalbergia sissoo - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fd70c39f4d425303420
Scientific name Dalbergia sissoo
Authority Roxb. ex DC.
First published in Prodr.2: 416 (1825)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Amerimnon sissoo (Roxb. ex DC.) Kuntze Revis. Gen. Pl.1: 159 (1891)
Pterocarpus sissoo Roxb. ex Wight & Arn. Prodr. Fl. Ind. Orient.1: 264 (1834)
Dalbergia pendula Ten. Rendiconto Accad. Sci. Soc. Borbon. Napoli1: 409 (1842)
Endespermum diversifolium Blume ex Miq. Fl. Ned. Ind.1(1): 128 (1855)

Common names Top

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Language Common/alternative name
English sissoo
English sissoo tree
English sissu
English sisoo
English shisham
English rose wood
English indian rosewood
English sisu
Arabic ساسم
Arabic سرسوع
German shesham
German sheesham
Persian شیشم
Persian سیسم
Persian جگ
French shisham
French sheesham
French sesham
French bois de sesham
French sissoo
Gujarati સીસમ
Hebrew דלברגיה
Hebrew סיסם
Hebrew סיסם הודי
Hindi शीशम
Japanese シッソノキ
Kannada ಸೀಸಂ
Korean 인디언 로즈우드
Korean 북인도황단
Malayalam ശിംശപാ
Malayalam ശിംശപ
Marathi शिसव
Burmese ကုလားပိတောက်
Nepali सिसौ
Punjabi ਟਾਹਲੀ
Punjab ٹاہلی
sd ٽالهي
Tamil சிசே மரம்
Telugu ఇరిడి
Telugu సిసూ
Urdu شیشم
Urdu ٹاہلی
Urdu ٹالی
Urdu indian rosewood
Chinese 印度黄檀
Chinese 印度黃檀
Chinese 印度檀
Chinese 降香
Chinese 茶檀

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Sudan
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Free State
      • Northern Provinces
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
  • Asia-temperate
    • Arabian Peninsula
      • Oman
    • China
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Palestine
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar
    • Malesia
      • Jawa
      • Sumatera
  • Southern America
    • Brazil
      • Brazil Southeast
    • Caribbean
      • Cuba
      • Dominican Republic
      • Leeward Islands
      • Puerto Rico
    • Central America
      • Panamá

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000172499
UNII 3LLA21QJ2X
Florida Plant Atlas 1447
USDA Plants DASI
Tropicos 13018086
INPN 447175
KEW urn:lsid:ipni.org:names:490469-1
The Plant List ild-1870
Open Tree Of Life 93966
NCBI Taxonomy 107308
Nature Serve 2.130140
IUCN Red List 62022617
IPNI 490469-1
iNaturalist 161584
GBIF 2968532
Freebase /m/02rn5sr
EPPO DAGSI
EOL 639922
USDA GRIN 13169
Wikipedia Dalbergia_sissoo
CMAUP NPO1830

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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Disease spectrum and its molecular characterisation in the lentil production system of lower-Indo Gangetic plains Nazneen H, Das R, Das A, Dutta S, Bhattacharya S, Patar S, Roy S, Gupta S, Kumar S Front Plant Sci 23-Feb-2024
PMCID:PMC10920269
doi:10.3389/fpls.2024.1199016
PMID:38463566
An appraisal of traditional knowledge of plant poisoning of livestock and its validation through acute toxicity assay in rats Rasool F, Nizamani ZA, Ahmad KS, Parveen F, Khan SA, Sabir N Front Pharmacol 14-Feb-2024
PMCID:PMC10900104
doi:10.3389/fphar.2024.1328133
PMID:38420196
Genetic Diversity and Structure of Terminalia bellerica (Gaertn. Roxb.) Population in India as Revealed by Genetic Analysis Umesh Kanna S, Parthiban KT, Senthilraja K, Venkatesan S, Udhaya Nandhini D, Mohan Kumar S, Dhasarathan M, Kumaresan P, Sai MJ, Raveendran M, Geethalakshmi V Plants (Basel) 06-Feb-2024
PMCID:PMC10892032
doi:10.3390/plants13040470
PMID:38498452
Prey selection by leopards (Panthera pardus fusca) in the mid‐hill region of Nepal Baral K, Bhandari S, Adhikari B, Kunwar RM, Sharma HP, Aryal A, Ji W Ecol Evol 05-Feb-2024
PMCID:PMC10844760
doi:10.1002/ece3.10924
PMID:38322006
Use of Trichoderma in the Production of Forest Seedlings Ferreira NC, Ramos ML, Gatto A Microorganisms 23-Jan-2024
PMCID:PMC10893047
doi:10.3390/microorganisms12020237
PMID:38399641
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
Apoptosis induction capability of silver nanoparticles capped with Acorus calamus L. and Dalbergia sissoo Roxb. Ex DC. against lung carcinoma cells Thakkar AB, Subramanian RB, Thakkar VR, Bhatt SV, Chaki S, Vaidya YH, Patel V, Thakor P Heliyon 15-Jan-2024
PMCID:PMC10831608
doi:10.1016/j.heliyon.2024.e24400
PMID:38304770
Effect of Crown Layers on Reproductive Effort and Success in Andromonoecious Aesculus indica (Wall. ex Camb.) Hook (Sapindaceae) in a Temperate Forest of Garhwal Himalaya Pradhan P, Sukumaran A, Khanduri VP, Singh B, Rawat D, Riyal MK, Kumar M, Pinto MM Plants (Basel) 10-Jan-2024
PMCID:PMC10818387
doi:10.3390/plants13020183
PMID:38256737
Investigating the phenology and interactions of competitive plant species co-occurring with invasive Lantana camara in Indian Himalayan Region Kumar A, Singh S, Kumar D, Singh RK, Gupta AK, Premkumar K, Chand HB, Kewat AK Sci Rep 03-Jan-2024
PMCID:PMC10764828
doi:10.1038/s41598-023-50287-x
PMID:38172161
LC–MS profiling, in vitro and in silico C-ABL kinase inhibitory approach to identify potential anticancer agents from Dalbergia sissoo leaves Naik HN, Kanjariya D, Parveen S, Ahmed I, Meena A, Patel H, Meena R, Jauhari S Sci Rep 02-Jan-2024
PMCID:PMC10761914
doi:10.1038/s41598-023-49995-1
PMID:38167560
Osteoarthritis in the Elderly Population: Preclinical Evidence of Nutrigenomic Activities of Flavonoids Naselli F, Bellavia D, Costa V, De Luca A, Raimondi L, Giavaresi G, Caradonna F Nutrients 28-Dec-2023
PMCID:PMC10780745
doi:10.3390/nu16010112
PMID:38201942
Electricity generation and oxidoreductase potential during dye discoloration by laccase-producing Ganoderma gibbosum in fungal fuel cell Umar A, Abid I, Antar M, Dufossé L, Hajji-Hedfi L, Elshikh MS, Shahawy AE, Abdel-Azeem AM Microb Cell Fact 14-Dec-2023
PMCID:PMC10720082
doi:10.1186/s12934-023-02258-0
PMID:38098010
Biogenic silver nanoparticles: Synthesis, applications and challenges in food sector with special emphasis on aquaculture Khursheed S, Dutta J, Ahmad I, Rather MA, Badroo IA, Bhat TA, Ahmad I, Amin A, Shah A, Qadri T, Habib H Food Chem X 07-Dec-2023
PMCID:PMC10740048
doi:10.1016/j.fochx.2023.101051
PMID:38144846
Chromosome-scale genomes of commercially important mahoganies, Swietenia macrophylla and Khaya senegalensis Sahu SK, Liu M, Wang G, Chen Y, Li R, Fang D, Sahu DN, Mu W, Wei J, Liu J, Zhao Y, Zhang S, Lisby M, Liu X, Xu X, Li L, Wang S, Liu H, He C Sci Data 25-Nov-2023
PMCID:PMC10676371
doi:10.1038/s41597-023-02707-w
PMID:38007506

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives
(2R,4R,6R)-4-hydroxy-2-methoxy-6-[(1S)-1-phenylprop-2-enyl]cyclohexan-1-one 162849289 Click to see COC1CC(CC(C1=O)C(C=C)C2=CC=CC=C2)O 260.33 unknown https://doi.org/10.1021/NP070478H
(2S,4R,5S)-4-hydroxy-5-methoxy-2-[(1R)-1-phenylprop-2-enyl]cyclohexan-1-one 11470966 Click to see COC1CC(=O)C(CC1O)C(C=C)C2=CC=CC=C2 260.33 unknown https://doi.org/10.1021/NP070478H
4-Hydroxy-2-methoxy-6-(1-phenylprop-2-enyl)cyclohexan-1-one 72965579 Click to see COC1CC(CC(C1=O)C(C=C)C2=CC=CC=C2)O 260.33 unknown https://doi.org/10.1021/NP070478H
4-Hydroxy-5-methoxy-2-(1-phenylprop-2-enyl)cyclohexan-1-one 72956785 Click to see COC1CC(=O)C(CC1O)C(C=C)C2=CC=CC=C2 260.33 unknown https://doi.org/10.1021/NP070478H
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Damascenine 21368 Click to see CNC1=C(C=CC=C1OC)C(=O)OC 195.21 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzophenones
Cearoin 3938139 Click to see COC1=C(C=C(C(=C1)O)C(=O)C2=CC=CC=C2)O 244.24 unknown https://doi.org/10.1021/NP070478H
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
2-(1-Phenylprop-2-enyl)benzene-1,4-diol 67642141 Click to see C=CC(C1=CC=CC=C1)C2=C(C=CC(=C2)O)O 226.27 unknown https://doi.org/10.1021/NP070478H
2-[(S)-1-Phenyl-2-propenyl]hydroquinone 24769835 Click to see C=CC(C1=CC=CC=C1)C2=C(C=CC(=C2)O)O 226.27 unknown https://doi.org/10.1021/NP070478H
2-methoxy-5-[(1S)-1-phenylprop-2-enyl]benzene-1,4-diol 162950293 Click to see COC1=C(C=C(C(=C1)O)C(C=C)C2=CC=CC=C2)O 256.30 unknown https://doi.org/10.1021/NP070478H
4-(1-Phenylprop-2-enyl)benzene-1,3-diol 72965285 Click to see C=CC(C1=CC=CC=C1)C2=C(C=C(C=C2)O)O 226.27 unknown https://doi.org/10.1021/NP070478H
4-[(1S)-1-phenylprop-2-enyl]benzene-1,3-diol 11447476 Click to see C=CC(C1=CC=CC=C1)C2=C(C=C(C=C2)O)O 226.27 unknown https://doi.org/10.1021/NP070478H
Obtusaquinol 10467594 Click to see COC1=C(C=C(C(=C1)O)C(C=C)C2=CC=CC=C2)O 256.30 unknown https://doi.org/10.1021/NP070478H
> Benzenoids / Benzene and substituted derivatives / Styrenes
(4R)-4-hydroxy-2,5-dimethoxy-4-[(E)-3-phenylprop-2-enyl]cyclohexa-2,5-dien-1-one 163188571 Click to see COC1=CC(=O)C(=CC1(CC=CC2=CC=CC=C2)O)OC 286.32 unknown https://doi.org/10.1021/NP070478H
(4S)-4-hydroxy-3-methoxy-4-[(E)-3-phenylprop-2-enyl]cyclohex-2-en-1-one 163194459 Click to see COC1=CC(=O)CCC1(CC=CC2=CC=CC=C2)O 258.31 unknown https://doi.org/10.1021/NP070478H
2,5-Dimethoxy-4-hydroxy-4-[(E)-3-phenyl-2-propenyl]-2,5-cyclohexadiene-1-one 24761040 Click to see COC1=CC(=O)C(=CC1(CC=CC2=CC=CC=C2)O)OC 286.32 unknown https://doi.org/10.1021/NP070478H
4-Hydroxy-2,5-dimethoxy-4-(3-phenylprop-2-enyl)cyclohexa-2,5-dien-1-one 163021936 Click to see COC1=CC(=O)C(=CC1(CC=CC2=CC=CC=C2)O)OC 286.32 unknown https://doi.org/10.1021/NP070478H
4-Hydroxy-3-methoxy-4-(3-phenylprop-2-enyl)cyclohex-2-en-1-one 72805767 Click to see COC1=CC(=O)CCC1(CC=CC2=CC=CC=C2)O 258.31 unknown https://doi.org/10.1021/NP070478H
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-7-epi-Syringaresinol 4'-glucoside 4486984 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
Acanthoside B 443024 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
Episyringaresinol 4'-O-beta-D-glncopyranoside 45482321 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Margolonone 189726 Click to see CC1=CC2=C(C=C1C(=O)O)C(=O)CC3C2(CCC(=O)C3(C)C)C 314.40 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
https://doi.org/10.1016/J.BMCL.2011.12.036
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3R,4S,5S,6R)-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-17-[(2S)-2-[(2S,3R,4S,5S,6R)-6-[[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-6-methylhept-5-en-2-yl]-12-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 21674162 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)O)O)O)O)C 1049.20 unknown https://doi.org/10.1021/NP070478H
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1076/PHBI.37.1.54.6310
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Estradiol 5757 Click to see CC12CCC3C(C1CCC2O)CCC4=C3C=CC(=C4)O 272.40 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1076/PHBI.37.1.54.6310
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1076/PHBI.37.1.54.6310
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1076/PHBI.37.1.54.6310
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
(1R,2S,4S,5S)-2-methoxy-5-[(1R)-1-phenylprop-2-enyl]cyclohexane-1,4-diol 11380002 Click to see COC1CC(C(CC1O)C(C=C)C2=CC=CC=C2)O 262.34 unknown https://doi.org/10.1021/NP070478H
2-Methoxy-5-(1-phenylprop-2-enyl)cyclohexane-1,4-diol 72824426 Click to see COC1CC(C(CC1O)C(C=C)C2=CC=CC=C2)O 262.34 unknown https://doi.org/10.1021/NP070478H
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4R,6S)-4-hydroxy-3-methoxy-6-[(1S)-1-phenylprop-2-enyl]cyclohex-2-en-1-one 162906650 Click to see COC1=CC(=O)C(CC1O)C(C=C)C2=CC=CC=C2 258.31 unknown https://doi.org/10.1021/NP070478H
(4R,6S)-4-hydroxy-6-[(1S)-1-phenylprop-2-enyl]cyclohex-2-en-1-one 162920647 Click to see C=CC(C1CC(C=CC1=O)O)C2=CC=CC=C2 228.29 unknown https://doi.org/10.1021/NP070478H
4-Hydroxy-3-methoxy-6-(1-phenylprop-2-enyl)cyclohex-2-en-1-one 72805766 Click to see COC1=CC(=O)C(CC1O)C(C=C)C2=CC=CC=C2 258.31 unknown https://doi.org/10.1021/NP070478H
4-Hydroxy-6-(1-phenylprop-2-enyl)cyclohex-2-en-1-one 85416296 Click to see C=CC(C1CC(C=CC1=O)O)C2=CC=CC=C2 228.29 unknown https://doi.org/10.1021/NP070478H
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3aR)-2,3,3abeta,4,5,9,9abeta,9balpha-Octahydro-4beta-acetoxy-6,9alpha-dimethyl-9beta-hydroxy-3-methylene-azuleno[4,5-b]furan-2-one 14466136 Click to see CC1=C2C=CC(C2C3C(C(C1)OC(=O)C)C(=C)C(=O)O3)(C)O 304.34 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(2E)-2-[(3,4-dihydroxyphenyl)methylidene]-4-methoxy-4-oxobutanoic acid 57390741 Click to see COC(=O)CC(=CC1=CC(=C(C=C1)O)O)C(=O)O 252.22 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
2-[(3,4-Dihydroxyphenyl)methylidene]-4-methoxy-4-oxobutanoic acid 76534893 Click to see COC(=O)CC(=CC1=CC(=C(C=C1)O)O)C(=O)O 252.22 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-2-(3,4-Dihydroxyphenyl)-6,7-dihydroxy-2,3-dihydrochromen-4-one 102196479 Click to see C1C(OC2=CC(=C(C=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP070478H
(2S)-6,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one 24769836 Click to see C1C(OC2=CC(=C(C=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1021/NP070478H
(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/NP070478H
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/10.1021/NP070478H
6,7-Dihydroxy-2-phenyl-2,3-dihydrochromen-4-one 70649071 Click to see C1C(OC2=CC(=C(C=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1021/NP070478H
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/NP070478H
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1021/NP070478H
Plathymenin 12314367 Click to see C1C(OC2=CC(=C(C=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP070478H
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Norartocarpetin 5481970 Click to see C1=CC(=C(C=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 286.24 unknown https://doi.org/10.1076/PHBI.37.1.54.6310
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12313332 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/10.1016/J.BMCL.2011.12.036
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
Kaempferol-3-O-rutinoside 5318767 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/10.1016/J.BMCL.2011.12.036
Rutin 5280805 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)O 610.50 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
Vitamin P 5293655 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)O 610.50 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(+)-Medicarpin 73067 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1021/NP070478H
(6aS,11aS)-9-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,4-diol 102184129 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4O)O 286.28 unknown https://doi.org/10.1021/NP070478H
3-Hydroxy-4,9-dimethoxypterocarpan 14077265 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4OC)O 300.30 unknown https://doi.org/10.1021/NP070478H
4-Hydroxymedicarpin 11536537 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4O)O 286.28 unknown https://doi.org/10.1021/NP070478H
6H-Benzofuro[3,2-c][1]benzopyran-3,10-diol, 6a,11a-dihydro-9-methoxy-, (6aS,11aS)- 44446857 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/NP070478H
9-Methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol 623060 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1021/NP070478H
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/NP070478H
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 5,7-dihydroxy-3-(4-hydroxyphenyl)-4-oxochromene-8-carboxylate 162867109 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C(=O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 476.40 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
https://doi.org/10.1076/PHBI.37.1.54.6310
Tectorigenin 5281811 Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1076/PHBI.37.1.54.6310
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
3-Genistein-8-C-glucoside 5472471 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 154496626 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
Genistein 8-C-glucoside 5281757 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
https://doi.org/10.1016/J.BMCL.2011.12.036
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-[4-[(2S,3R,4S,5R,6R)-6-[[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-5-hydroxy-6,7-dimethoxychromen-4-one 162956771 Click to see COC1=C(C(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O)OC 608.50 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
3-[4-[(2S,3R,4S,5R,6S)-6-[[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-5-hydroxy-7-methoxychromen-4-one 162949654 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
3-[4-[(2S,3R,4S,5S,6R)-6-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-5-hydroxy-6,7-dimethoxychromen-4-one 162956770 Click to see COC1=C(C(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O)OC 608.50 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
3-[4-[(2S,3R,4S,5S,6R)-6-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-5-hydroxy-7-methoxychromen-4-one 162949655 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
3-[4-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-5-hydroxy-6,7-dimethoxychromen-4-one 162956769 Click to see COC1=C(C(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O)OC 608.50 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
3-[4-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-5-hydroxy-7-methoxychromen-4-one 162949653 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
5-hydroxy-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(2,4,5-trimethoxyphenyl)chromen-4-one 57390787 Click to see COC1=CC(=C(C=C1C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 536.50 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
5-Hydroxy-6-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(2,4,5-trimethoxyphenyl)chromen-4-one 138644962 Click to see COC1=CC(=C(C=C1C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 536.50 unknown https://doi.org/10.1016/0031-9422(73)85048-4
https://doi.org/10.1016/J.BMCL.2011.12.036
5-hydroxy-7-methoxy-3-[4-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 154497291 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
5-hydroxy-8-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(2,4,5-trimethoxyphenyl)chromen-4-one 14779765 Click to see COC1=CC(=C(C=C1C2=COC3=C(C2=O)C(=CC(=C3OC)OC4C(C(C(C(O4)CO)O)O)O)O)OC)OC 536.50 unknown https://doi.org/10.1016/0031-9422(80)87054-3
5-hydroxy-8-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-3-(2,4,5-trimethoxyphenyl)chromen-4-one 102077547 Click to see COC1=CC(=C(C=C1C2=COC3=C(C2=O)C(=CC(=C3OC)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)OC)OC 698.60 unknown https://doi.org/10.1016/0031-9422(80)87054-3
5-Hydroxy-8-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(2,4,5-trimethoxyphenyl)chromen-4-one 14779764 Click to see COC1=CC(=C(C=C1C2=COC3=C(C2=O)C(=CC(=C3OC)OC4C(C(C(C(O4)CO)O)O)O)O)OC)OC 536.50 unknown https://doi.org/10.1016/0031-9422(80)87054-3
5-Hydroxy-8-methoxy-7-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-3-(2,4,5-trimethoxyphenyl)chromen-4-one 163068699 Click to see COC1=CC(=C(C=C1C2=COC3=C(C2=O)C(=CC(=C3OC)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)OC)OC 698.60 unknown https://doi.org/10.1016/0031-9422(80)87054-3
7-[(2-O-D-Apio-beta-D-furanosyl-beta-D-glucopyranosyl)oxy]-5-hydroxy-3-(4-methoxyphenyl)-4H-1-benzopyran-4-one 14236609 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
https://doi.org/10.1016/J.BMCL.2011.12.036
7-[(2S,3R,4S,5R,6R)-6-[[(2R,3S,4R)-4-[[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-(4-methoxyphenyl)chromen-4-one 163084827 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC5C(C(CO5)(COC6C(C(CO6)(CO)O)O)O)O)O)O)O 710.60 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
7-[(2S,3R,4S,5R,6R)-6-[[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-(4-hydroxyphenyl)-6-methoxychromen-4-one 162886884 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
7-[(2S,3R,4S,5R,6R)-6-[[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-(4-methoxyphenyl)chromen-4-one 161291495 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-(4-hydroxyphenyl)-6-methoxychromen-4-one 5323552 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-6-methoxy-3-(2,4,5-trimethoxyphenyl)chromen-4-one 57399533 Click to see COC1=CC(=C(C=C1C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)OC)OC 668.60 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
7-[(2S,3R,4S,5S,6R)-6-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-(4-hydroxyphenyl)-6-methoxychromen-4-one 23786445 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
7-[(2S,3R,4S,5S,6R)-6-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-(4-methoxyphenyl)chromen-4-one 45359960 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
7-[(2S,3R,4S,5S,6R)-6-[[(2S,3R,4S)-4-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxyoxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-(4-methoxyphenyl)chromen-4-one 163084826 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC5C(C(CO5)(COC6C(C(CO6)(CO)O)O)O)O)O)O)O 710.60 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
7-[[6-O-(5-O-D-Apio-beta-D-furanosyl-D-apio-beta-D-furanosyl)-beta-D-glucopyranosyl]oxy]-4'-methoxy-5-hydroxyisoflavone 57396079 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC5C(C(CO5)(COC6C(C(CO6)(CO)O)O)O)O)O)O)O 710.60 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
https://doi.org/10.1016/J.BMCL.2011.12.036
7-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-(4-hydroxyphenyl)-6-methoxychromen-4-one 20980952 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
Genistin 5281377 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
Lanceolarin 5492234 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
Prunetin 4'-O-glucoside 16398538 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
Prunetrin 5918474 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1016/S0031-9422(01)00195-9
Sissotrin 5280781 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
Sissotrin with HPLC, 99+% [5928-26-7] 45934014 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1076/PHBI.37.1.54.6310
Sissotrine 5358913 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-O-Methylorobol 5319744 Click to see COC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(+)-Vestitol 177149 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown https://doi.org/10.1021/NP070478H
Vestitol 92503 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown https://doi.org/10.1021/NP070478H
Vestitol, (-)- 182259 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown https://doi.org/10.1021/NP070478H
> 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/NP070478H
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/NP070478H
Pratensein 5281803 Click to see COC1=C(C=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxyformononetin 5280551 Click to see COC1=CC(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown https://doi.org/10.1021/NP070478H
Biochanin A 5280373 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O 284.26 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
https://doi.org/10.1076/PHBI.37.1.54.6310
Caviunin 6708635 Click to see COC1=CC(=C(C=C1C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O)OC)OC 374.30 unknown https://doi.org/10.1016/J.BMCL.2011.12.036
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/NP070478H
Irisolidone 5281781 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O 314.29 unknown https://doi.org/10.1076/PHBI.37.1.54.6310
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Muningin 252471 Click to see COC1=C(C(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)O)OC)O 314.29 unknown https://doi.org/10.1076/PHBI.37.1.54.6310
Prunetin 5281804 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1076/PHBI.37.1.54.6310
> 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/NP070478H
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/NP070478H
2',3,4,4'-tetrahydroxy Chalcone 2483 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O)O 272.25 unknown https://doi.org/10.1021/NP070478H
Butein 5281222 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O)O 272.25 unknown https://doi.org/10.1021/NP070478H
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/10.1021/NP070478H
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/10.1021/NP070478H
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
3-Methoxy-4-(3-phenyl-2-propenyl)-1,2-benzenediol 11777169 Click to see COC1=C(C=CC(=C1O)O)CC=CC2=CC=CC=C2 256.30 unknown https://doi.org/10.1021/NP070478H
3-Methoxy-4-(3-phenylprop-1-enyl)benzene-1,2-diol 163025154 Click to see COC1=C(C=CC(=C1O)O)C=CCC2=CC=CC=C2 256.30 unknown https://doi.org/10.1021/NP070478H
> Phenylpropanoids and polyketides / Neoflavonoids / Dalbergiones
(5R,6S)-5,6-dihydroxy-2-methoxy-5-[(1R)-1-phenylprop-2-enyl]cyclohex-2-ene-1,4-dione 163055796 Click to see COC1=CC(=O)C(C(C1=O)O)(C(C=C)C2=CC=CC=C2)O 288.29 unknown https://doi.org/10.1021/NP070478H
(S)-4-Methoxydalbergione 10400054 Click to see COC1=CC(=O)C(=CC1=O)C(C=C)C2=CC=CC=C2 254.28 unknown https://doi.org/10.1021/NP070478H
(S)-4'-Hydroxy-4-methoxydalbergione 44257558 Click to see COC1=CC(=O)C(=CC1=O)C(C=C)C2=CC=C(C=C2)O 270.28 unknown https://doi.org/10.1021/NP070478H
2,3-Dihydroxy-2-(1-phenyl-2-propenyl)-5-methoxy-5-cyclohexene-1,4-dione 24761039 Click to see COC1=CC(=O)C(C(C1=O)O)(C(C=C)C2=CC=CC=C2)O 288.29 unknown https://doi.org/10.1021/NP070478H
4-Methoxydalbergione 99926 Click to see COC1=CC(=O)C(=CC1=O)C(C=C)C2=CC=CC=C2 254.28 unknown https://doi.org/10.1021/NP070478H
Dalbergione 3015195 Click to see C=CC(C1=CC=CC=C1)C2=CC(=O)C=CC2=O 224.25 unknown https://doi.org/10.1021/NP070478H
Dalbergione, 4-methoxy-4'-hydroxy- 3950721 Click to see COC1=CC(=O)C(=CC1=O)C(C=C)C2=CC=C(C=C2)O 270.28 unknown https://doi.org/10.1021/NP070478H
S-dalbergione 44448235 Click to see C=CC(C1=CC=CC=C1)C2=CC(=O)C=CC2=O 224.25 unknown https://doi.org/10.1021/NP070478H
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
Dalbergin 442768 Click to see COC1=C(C=C2C(=CC(=O)OC2=C1)C3=CC=CC=C3)O 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Pinosylvin 5280457 Click to see C1=CC=C(C=C1)C=CC2=CC(=CC(=C2)O)O 212.24 unknown via CMAUP database
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database

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