Helicteres angustifolia - Unknown
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Internal ID UUID64401ff73cdff905130117
Scientific name Helicteres angustifolia
Authority L.
First published in Sp. Pl. : 963 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Helicteres parviflora Ridl. J. Straits Branch Roy. Asiat. Soc. 59: 77 (1911)
Helicteres virgata Wall. ex G.Don Gen. Hist. 1: 508 (1831)
Helicteres salicifolia C.Presl Reliq. Haenk. 2: 139 (1835)
Oudemansia virgata (Wall. ex G.Don) Hassk. Retzia 1: 134 (1855)
Oudemansia javensis var. angustifolia (L.) Hassk. Retzia 1: 134 1855
Helicteres angustifolia var. virgata Kuntze Revis. Gen. Pl. 1: 79 1891
Helicteres angustifolia var. acuminatissima Kuntze Revis. Gen. Pl. 1: 79 1891
Helicteres angustifolia var. gaudichaudii Kuntze Revis. Gen. Pl. 1: 79 1891
Helicteres angustifolia var. meyeniana Kuntze Revis. Gen. Pl. 1: 79 1891
Helicteres angustifolia var. naumanniana Kuntze Revis. Gen. Pl. 1: 79 1891
Helicteres angustifolia var. obtusa (Wall. ex Kurz) Pierre Fl. Forest. Cochinch. 13: t. 211, f. 14–25 t. 211, f. 14-25 1889

Common names Top

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Language Common/alternative name
Chinese 山油麻
Chinese 山芝麻
Chinese 坡油麻

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Malaya
      • Philippines

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000718077
Tropicos 30401866
KEW urn:lsid:ipni.org:names:823419-1
The Plant List kew-2843159
Open Tree Of Life 283046
NCBI Taxonomy 190244
IPNI 823419-1
iNaturalist 556220
GBIF 5547507
EPPO HCTAN
EOL 2889498
USDA GRIN 423432
CMAUP NPO7216

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
Purification and Structural Characterization of Polysaccharides from Polygonum multiflorum Thunb. and Their Immunostimulatory Activity in RAW264.7 Cells Gou Y, Gu D, Fan J, Yang J, Zan K, Liu J, Jin H, Wang Y, Wei F, Ma S Foods 19-Mar-2024
PMCID:PMC10969798
doi:10.3390/foods13060932
PMID:38540922
Correction: Zhang et al. Genotype–Environment Interaction and Horizontal and Vertical Distributions of Heartwood for Acacia melanoxylon R.Br. Genes 2023, 14, 1299 Zhang R, Zeng B, Chen T, Hu B Genes (Basel) 09-Feb-2024
PMCID:PMC10887675
doi:10.3390/genes15020221
PMID:38397249
Mulberry Leaf Polysaccharides Attenuate Oxidative Stress Injury in Peripheral Blood Leukocytes by Regulating Endoplasmic Reticulum Stress Jiang W, Lin Y, Qian L, Lu S, Shen H, Ge X, Miao L Antioxidants (Basel) 23-Jan-2024
PMCID:PMC10886326
doi:10.3390/antiox13020136
PMID:38397734
Editorial: Oxidative stress link associated with mitochondrial bioenergetics: relevance in cell aging and age-related pathologies Kalra RS, Kumar S, Tomar D Front Cell Dev Biol 05-Sep-2023
PMCID:PMC10509040
doi:10.3389/fcell.2023.1273420
PMID:37736499
Bioactivity-guided fractionation of Helicteres angustifolia L. extract and its molecular evidence for tumor suppression Li K, Sun S, Xiao L, Zhang Z Front Cell Dev Biol 22-Jun-2023
PMCID:PMC10323433
doi:10.3389/fcell.2023.1157172
PMID:37427379
Genotype–Environment Interaction and Horizontal and Vertical Distributions of Heartwood for Acacia melanoxylon R.Br Zhang R, Zeng B, Chen T, Hu B Genes (Basel) 20-Jun-2023
PMCID:PMC10298161
doi:10.3390/genes14061299
PMID:37372479
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
Antibacterial and Antifungal Terpenes from the Medicinal Angiosperms of Asia and the Pacific: Haystacks and Gold Needles Wiart C, Kathirvalu G, Raju CS, Nissapatorn V, Rahmatullah M, Paul AK, Rajagopal M, Sathiya Seelan JS, Rusdi NA, Lanting S, Sulaiman M Molecules 04-May-2023
PMCID:PMC10180233
doi:10.3390/molecules28093873
PMID:37175283
Ethnobotanical study on herbal tea drinks in Guangxi, China Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064729
doi:10.1186/s13002-023-00579-3
PMID:37004116
Specialized metabolites from plants as a source of new multi-target antiviral drugs: a systematic review Ponticelli M, Bellone ML, Parisi V, Iannuzzi A, Braca A, de Tommasi N, Russo D, Sileo A, Quaranta P, Freer G, Pistello M, Milella L Phytochem Rev 12-Mar-2023
PMCID:PMC10008214
doi:10.1007/s11101-023-09855-2
PMID:37359711
Multifunctional Roles of Betulinic Acid in Cancer Chemoprevention: Spotlight on JAK/STAT, VEGF, EGF/EGFR, TRAIL/TRAIL-R, AKT/mTOR and Non-Coding RNAs in the Inhibition of Carcinogenesis and Metastasis Farooqi AA, Turgambayeva A, Tashenova G, Tulebayeva A, Bazarbayeva A, Kapanova G, Abzaliyeva S Molecules 21-Dec-2022
PMCID:PMC9822120
doi:10.3390/molecules28010067
PMID:36615262
Structure–immunomodulatory activity relationships of dietary polysaccharides Chen R, Xu J, Wu W, Wen Y, Lu S, El-Seedi HR, Zhao C Curr Res Food Sci 28-Aug-2022
PMCID:PMC9445227
doi:10.1016/j.crfs.2022.08.016
PMID:36082139
Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China Lu Z, Chen H, Lin C, Ou G, Li J, Xu W J Ethnobiol Ethnomed 21-Jun-2022
PMCID:PMC9210605
doi:10.1186/s13002-022-00544-6
PMID:35729593
A Comprehensive Review of Rosmarinic Acid: From Phytochemistry to Pharmacology and Its New Insight Guan H, Luo W, Bao B, Cao Y, Cheng F, Yu S, Fan Q, Zhang L, Wu Q, Shan M Molecules 20-May-2022
PMCID:PMC9143754
doi:10.3390/molecules27103292
PMID:35630768
Metabolic stimulation-elicited transcriptional responses and biosynthesis of acylated triterpenoids precursors in the medicinal plant Helicteres angustifolia Huang Y, An W, Yang Z, Xie C, Liu S, Zhan T, Pan H, Zheng X BMC Plant Biol 25-Feb-2022
PMCID:PMC8876399
doi:10.1186/s12870-022-03429-8
PMID:35216551

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 / Naphthalenes / Naphthoquinones
(4R)-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5(13),6,8-tetraene-10,11-dione 139071911 Click to see CC1COC2=C(C(=O)C(=O)C3=C(C=CC1=C32)C)C 242.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
https://doi.org/10.1016/0031-9422(90)80061-K
(4R)-6-methoxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13)-tetraene-10,11-dione 162876729 Click to see CC1COC2=C(C(=O)C(=O)C3=C2C1=C(C=C3C)OC)C 272.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
https://doi.org/10.1016/0031-9422(90)80061-K
(4S)-6-hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13)-tetraene-10,11-dione 73353443 Click to see CC1COC2=C(C(=O)C(=O)C3=C2C1=C(C=C3C)O)C 258.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
https://doi.org/10.1016/0031-9422(90)80061-K
6-Methoxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13)-tetraene-10,11-dione 14544217 Click to see CC1COC2=C(C(=O)C(=O)C3=C2C1=C(C=C3C)OC)C 272.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
https://doi.org/10.1016/0031-9422(90)80061-K
Mansonone E 94303 Click to see CC1COC2=C(C(=O)C(=O)C3=C(C=CC1=C32)C)C 242.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
https://doi.org/10.1016/0031-9422(90)80061-K
Mansonone F 94304 Click to see CC1=C2C3=C(C=C1)C(=COC3=C(C(=O)C2=O)C)C 240.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
https://doi.org/10.1016/0031-9422(90)80061-K
Mansonone H 615515 Click to see CC1COC2=C(C(=O)C(=O)C3=C2C1=C(C=C3C)O)C 258.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
https://doi.org/10.1016/S0031-9422(00)81461-2
https://doi.org/10.1016/0031-9422(90)80061-K
> Benzenoids / Phenols / Methoxyphenols
3-(4-Hydroxy-3-methoxyphenyl)-prop-2-enol 9983 Click to see COC1=C(C=CC(=C1)C=CCO)O 180.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Coniferyl alcohol 1549095 Click to see COC1=C(C=CC(=C1)C=CCO)O 180.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
4-[6-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 234817 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Syringaresinol 100067 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Lariciresinol 23815394 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-3-furanmethanol 134203 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Methyl 3-phenylpropionate 7643 Click to see COC(=O)CCC1=CC=CC=C1 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Heptadecanoic acid, 4-methyl- 5319673 Click to see CCCCCCCCCCCCCC(C)CCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4As,8aS)-1-[(3S)-5-hydroxy-3-methylpentyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 11130717 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCO 310.50 unknown via CMAUP database
(3S)-5-[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 93233226 Click to see CC1=CC(=O)C2C(CCCC2(C1CCC(C)CC(=O)O)C)(C)C 320.50 unknown via CMAUP database
(4aalpha)-2-Hydroxy-2beta,5,5,8abeta-tetramethyldecalin-1beta-((R)-3-methylvaleric acid) 11868539 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)O 324.50 unknown via CMAUP database
Labdanolic acid 11186394 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)O 324.50 unknown via CMAUP database
methyl (3S)-5-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoate 7057547 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)OC 338.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1,2-Naphthalenedione, 6-hydroxy-3,8-dimethyl-5-(1-methylethyl)- 608583 Click to see CC1=CC2=C(C(=CC(=C2C(C)C)O)C)C(=O)C1=O 244.28 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Ledol 92812 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aS,5bR,7aR,9S,11aR,11bR,13aR,13bR)-5a-(benzoyloxymethyl)-9-hydroxy-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 11692717 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)O)C)C(=O)O 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
(1R,3aS,5aS,5bR,7aR,9S,11aS,11bR,13aR,13bS)-9-acetyloxy-5a-(benzoyloxymethyl)-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 163035404 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)OC(=O)C)C)C(=O)O 618.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 51892422 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
[(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 479957 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)CO 484.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
[3a-(Hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 3129301 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)CO 484.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
5a-(Benzoyloxymethyl)-9-hydroxy-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 73063852 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)O)C)C(=O)O 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
9-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 74340583 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)C(=O)O 618.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
https://doi.org/10.1002/CBDV.200890053
9-Acetyloxy-5a-(benzoyloxymethyl)-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 73201167 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)OC(=O)C)C)C(=O)O 618.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
CID 21120946 21120946 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)OC(=O)C)C)C(=O)OC 632.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Helicteric acid 15940296 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)OC(=O)C)C)C(=O)O 618.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
methyl (1R,3aS,5aS,5bR,7aR,9S,11aR,11bR,13aR,13bR)-5a-(benzoyloxymethyl)-9-hydroxy-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 11685744 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)O)C)C(=O)OC 590.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
methyl (1R,3aS,5aS,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-acetyloxy-5a-[(4-hydroxybenzoyl)oxymethyl]-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 102186522 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=C(C=C6)O)C)(C)C)OC(=O)C)C)C(=O)OC 648.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Methyl 10-acetyloxy-6a-(benzoyloxymethyl)-2,2,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 5319672 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC)COC(=O)C6=CC=CC=C6)C)C 632.90 unknown via CMAUP database
Methyl 5a-(benzoyloxymethyl)-9-hydroxy-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 73061531 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)O)C)C(=O)OC 590.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Methyl 9-acetyloxy-5a-[(4-hydroxybenzoyl)oxymethyl]-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 163069808 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=C(C=C6)O)C)(C)C)OC(=O)C)C)C(=O)OC 648.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Methyl helicterate 5319671 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)OC(=O)C)C)C(=O)OC 632.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Methyl helicterilate 128136 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC)COC(=O)C6=CC=CC=C6)C)C 632.90 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Pyracrenic acid 6439576 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)C(=O)O 618.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
https://doi.org/10.1002/CBDV.200890053
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
(8S,9R,10S,13S,14S,16R,17R)-2,16-dihydroxy-4,4,10,13-tetramethyl-17-[(2R,5R)-2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl]-7,8,9,12,14,15,16,17-octahydrocyclopenta[a]phenanthrene-3,11-dione 163020405 Click to see CC1(C2=CCC3C4CC(C(C4(CC(=O)C3C2(C=C(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C 518.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
2,16-Dihydroxy-4,4,10,13-tetramethyl-17-(2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl)-7,8,9,12,14,15,16,17-octahydrocyclopenta[a]phenanthrene-3,11-dione 163020404 Click to see CC1(C2=CCC3C4CC(C(C4(CC(=O)C3C2(C=C(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C 518.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Tetrahydroxy bile acids, alcohols and derivatives
(2S,8S,9R,10S,13S,14S,16R,17R)-17-[(E,2R)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-2,16-dihydroxy-4,4,10,13-tetramethyl-1,2,7,8,9,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,11-dione 163066852 Click to see CC1(C2=CCC3C4CC(C(C4(CC(=O)C3C2(CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C 502.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
17-(2,6-Dihydroxy-6-methyl-3-oxohept-4-en-2-yl)-2,16-dihydroxy-4,4,10,13-tetramethyl-1,2,7,8,9,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,11-dione 163066851 Click to see CC1(C2=CCC3C4CC(C(C4(CC(=O)C3C2(CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C 502.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
(8S,9R,10R,13R,14S,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-17-[(2R,5S)-2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl]-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthrene-3,11-dione 57402770 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2C=C(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C 532.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
[6-hydroxy-6-(16-hydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2-sulfooxy-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methyl-5-oxohept-3-en-2-yl] acetate 73241701 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)OS(=O)(=O)O)C)C)C)O)O 638.80 unknown https://doi.org/10.1248/CPB.54.1605
cucurbitacin B 2-sulfate 16093748 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)OS(=O)(=O)O)C)C)C)O)O 638.80 unknown https://doi.org/10.1248/CPB.54.1605
Cucurbitacin D 5281318 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 516.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Cucurbitacin J 441819 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2C=C(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C 532.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids
(2R,3R,7R,8S,9S,10R,13S,14S,17S)-17-[(1S)-1-hydroxy-2-methoxyethyl]-3-methoxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-2,7-diol 102186523 Click to see CC12CCC3C(C1CCC2C(COC)O)C(C=C4C3(CC(C(C4)OC)O)C)O 394.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
17-(1-hydroxy-2-methoxyethyl)-3-methoxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-2,7-diol 162855230 Click to see CC12CCC3C(C1CCC2C(COC)O)C(C=C4C3(CC(C(C4)OC)O)C)O 394.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2S,8S,9R,10R,13R,14S,16R,17R)-16-hydroxy-4,4,9,13,14-pentamethyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-[(2R,5R)-2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl]-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 163007626 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C 696.80 unknown https://doi.org/10.1248/CPB.54.1605
[6-hydroxy-6-[16-hydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methyl-5-oxohept-3-en-2-yl] acetate 72968961 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)C)O)O 720.80 unknown https://doi.org/10.1248/CPB.54.1605
16-hydroxy-4,4,9,13,14-pentamethyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-(2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 73241702 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C 696.80 unknown https://doi.org/10.1248/CPB.54.1605
17-(2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl)-16-hydroxy-4,4,9,13,14-pentamethyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 73804168 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 678.80 unknown https://doi.org/10.1248/CPB.54.1605
Arvenin I 6441104 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)C)O)O 720.80 unknown https://doi.org/10.1248/CPB.54.1605
arvenin III 21579640 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 678.80 unknown https://doi.org/10.1248/CPB.54.1605
> 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/10.1016/J.PHYTOCHEM.2006.03.005
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Organoheterocyclic compounds / Naphthofurans
(3aS,5aR,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran 12838593 Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C 236.39 unknown via CMAUP database
8,12-Epoxy-13,14,15,16-tetranorlabdane 11861328 Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C 236.39 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dihydrodehydrodiconiferyl alcohol 384679 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-(3,4-Dimethoxyphenyl)-2-propenal 107557 Click to see COC1=C(C=C(C=C1)C=CC=O)OC 192.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
3,4-Dimethoxy cinnamaldehyde 5375268 Click to see COC1=C(C=C(C=C1)C=CC=O)OC 192.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid 639655 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
3-(3,4-dihydroxyphenyl)-2-[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid 5099 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Rosmarinic acid 5281792 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
6,10,11-Trihydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(13),4,9,11-tetraen-3-one 75059643 Click to see CC1CC(C2=C(C(=O)OC3=C2C1=C(C(=C3C)O)O)C)O 276.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Vcbhabvpyyfxjs-xrgyyrrgsa- 44631546 Click to see CC1CC(C2=C(C(=O)OC3=C2C1=C(C(=C3C)O)O)C)O 276.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> 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 via CMAUP database
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 via CMAUP database
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 via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-8-O-glucuronides
(2S,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]oxy-3,4-dihydroxy-5-sulfooxyoxane-2-carboxylic acid 163106804 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)OS(=O)(=O)O)O 542.40 unknown https://doi.org/10.3987/COM-94-6710
(2S,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-3,4-dihydroxy-5-sulfooxyoxane-2-carboxylic acid 5318672 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)OS(=O)(=O)O 556.50 unknown https://doi.org/10.3987/COM-94-6710
methyl (2S,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate 163193559 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)OC)O)O)O 490.40 unknown https://doi.org/10.3987/COM-94-6710
Methyl 6-[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate 162898551 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)OC)O)O)O 490.40 unknown https://doi.org/10.3987/COM-94-6710
> 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-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 5315208 Click to see C1C(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 596.50 unknown via CMAUP database
3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 42613954 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)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown via CMAUP database
3-[(6-O-beta-D-Xylopyranosyl-beta-D-glucopyranosyl)oxy]-4',5,7-trihydroxy-3'-methoxyflavone 102148697 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
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.PHYTOCHEM.2006.03.005
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.PHYTOCHEM.2006.03.005
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 via CMAUP database
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 via CMAUP database
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
Myricetin-3-O-rutinoside 21577860 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)O 626.50 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
[5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-8-yl] (2S,3S,4S,5R,6R)-3,4,5,6-tetrahydroxyoxane-2-carboxylate 163003716 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC(=O)C4C(C(C(C(O4)O)O)O)O)O 492.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
[5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-8-yl] 3,4,5,6-tetrahydroxyoxane-2-carboxylate 163003715 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC(=O)C4C(C(C(C(O4)O)O)O)O)O 492.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown via CMAUP database
Ermanin 5352001 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,8-Dihydroxy-7,4'-dimethoxyflavone 15289454 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)O 314.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown via CMAUP database
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-Phenylpropionic acid 107 Click to see C1=CC=C(C=C1)CCC(=O)O 150.17 unknown via CMAUP database

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