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Rubia wallichiana

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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 UUID643feb51371e3341839637
Scientific name Rubia wallichiana
Authority Decne.
First published in Mém. Couronnés Acad. Roy. Sci. Bruxelles (4to) 12: 61 (1837)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rubia asperrima Decne. Mém. Couronnés Acad. Roy. Sci. Bruxelles (4to) 12: 61 (1837)

Common names Top

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Language Common/alternative name
Chinese 多花茜草
Chinese 多花茜草（光垄茜草）
Chinese 小红藤
Chinese 茜草
Chinese 三爪龙
Chinese 红丝线

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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • Nepal
      • West Himalaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000298664
Tropicos 100252738
KEW urn:lsid:ipni.org:names:765383-1
The Plant List kew-180449
Open Tree Of Life 3872642
NCBI Taxonomy 1905583
IPNI 765383-1
GBIF 2892342
EOL 1108068
CMAUP NPO3011

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
Arula-7 powder improves diarrhea and intestinal epithelial tight junction function associated with its regulation of intestinal flora in calves infected with pathogenic Escherichia coli O1 Chen H, Jia Z, He M, Chen A, Zhang X, Xu J, Wang C Microbiome 05-Aug-2023
PMCID:PMC10403850
doi:10.1186/s40168-023-01616-9
PMID:37542271
Microbial and Plant Derived Low Risk Pesticides Having Nematocidal Activity Evidente A Toxins (Basel) 03-Dec-2022
PMCID:PMC9787815
doi:10.3390/toxins14120849
PMID:36548747
Current advances on the phytochemical composition, pharmacologic effects, toxicology, and product development of Phyllanthi Fructus Yan X, Li Q, Jing L, Wu S, Duan W, Chen Y, Chen D, Pan X Front Pharmacol 19-Oct-2022
PMCID:PMC9626985
doi:10.3389/fphar.2022.1017268
PMID:36339628
Ethnoveterinary Survey Conducted in Baiku Yao Communities in Southwest China Luo B, Hu Q, Lai K, Bhatt A, Hu R Front Vet Sci 25-Jan-2022
PMCID:PMC8822042
doi:10.3389/fvets.2021.813737
PMID:35146017
Reusing wasteroot of Rubia wallichiana dyeing from Monpa of Tibet in China Yang R, Zhang Y, Ranjitkar S, Li M, Guo Y, Yan X, Wang C, Stepp JR, Yang L Sci Rep 12-Jul-2021
PMCID:PMC8275625
doi:10.1038/s41598-021-93848-8
PMID:34253840
Monpa, memory, and change: an ethnobotanical study of plant use in Mêdog County, South-east Tibet, China Li S, Zhang Y, Guo Y, Yang L, Wang Y J Ethnobiol Ethnomed 30-Jan-2020
PMCID:PMC6993401
doi:10.1186/s13002-020-0355-7
PMID:32000826
1,4-Naphthoquinone Triggers Nematode Lethality by Inducing Oxidative Stress and Activating Insulin/IGF Signaling Pathway in Caenorhabditis elegans Wang J, Zeng G, Huang X, Wang Z, Tan N Molecules 13-May-2017
PMCID:PMC6154497
doi:10.3390/molecules22050798
PMID:28505088
Traditional use and management of NTFPs in Kangchenjunga Landscape: implications for conservation and livelihoods Uprety Y, Poudel RC, Gurung J, Chettri N, Chaudhary RP J Ethnobiol Ethnomed 03-May-2016
PMCID:PMC4855762
doi:10.1186/s13002-016-0089-8
PMID:27142597
Biologically active arborinane-type triterpenoids and anthraquinones from Rubia yunnanensis. Fan JT, Kuang B, Zeng GZ, Zhao SM, Ji CJ, Zhang YM, Tan NH J Nat Prod 28-Oct-2011
doi:10.1021/NP2002918
PMID:21973054
Antibacterial activity of anthraquinone derivatives from Heterophyllaea pustulata (Rubiaceae). Comini LR, Montoya SC, Páez PL, Argüello GA, Albesa I, Cabrera JL J Photochem Photobiol B 07-Feb-2011
doi:10.1016/J.JPHOTOBIOL.2010.09.009
PMID:20965744
1,3-Dihydr­oxy-2-methoxy­methyl-9,10-anthraquinone from Rennellia elliptica Korth. Ismail NH, Osman CP, Ahmad R, Awang K, Ng SW Acta Crystallogr Sect E Struct Rep Online 29-May-2009
PMCID:PMC2969543
doi:10.1107/S1600536809017607
PMID:21583274
Cytotoxic Anthraquinones from the Stems of Rubia wallichiana Decne Tian‐Shung Wu, Dau‐Min Lin, Li‐Shian Shi, Amooru Gangaiah Damu, Ping‐Chung Kuo, Yao‐Hau Kuo Wiley 28-Jul-2005
doi:10.1002/CHIN.200403232
Cytotoxic anthraquinones from the stems of Rubia wallichiana Decne. Wu TS, Lin DM, Shi LS, Damu AG, Kuo PC, Kuo YH Chem Pharm Bull (Tokyo) 01-Aug-2003
doi:10.1248/CPB.51.948
PMID:12913233
Triterpenoids from Rubia yunnanensis. Liou MJ, Wu TS J Nat Prod 01-Sep-2002
doi:10.1021/NP020038K
PMID:12350148

Phytochemical Profile Top

Add a new one!
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 / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
2-Anthracenecarboxylic acid, 9,10-dihydro-1,3-dihydroxy-9,10-dioxo-, methyl ester 149791 Click to see COC(=O)C1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 298.25 unknown https://doi.org/10.1248/CPB.51.948
Methyl 1-hydroxy-9,10-dioxoanthracene-2-carboxylate 2870897 Click to see COC(=O)C1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 282.25 unknown https://doi.org/10.1248/CPB.51.948
Munjistin 1-methyl ether 101939212 Click to see COC1=C2C(=CC(=C1C(=O)O)O)C(=O)C3=CC=CC=C3C2=O 298.25 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
1-hydroxy-2-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyanthracene-9,10-dione 162962165 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)C(=O)C5=CC=CC=C5C4=O)O)CO)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1248/CPB.51.948
1-Hydroxy-2-(hydroxymethyl)-3-methoxyanthracene-9,10-dione 10085264 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3C2=O)O)CO 284.26 unknown https://doi.org/10.1248/CPB.51.948
1-Hydroxy-2-methoxyanthraquinone 80103 Click to see COC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown https://doi.org/10.1248/CPB.51.948
1-hydroxy-2-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyanthracene-9,10-dione 162920856 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 548.50 unknown https://doi.org/10.1248/CPB.51.948
1-Hydroxy-2-methyl-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyanthracene-9,10-dione 53463989 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 548.50 unknown https://doi.org/10.1248/CPB.51.948
1-Hydroxy-2-methylanthraquinone 160817 Click to see CC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 238.24 unknown https://doi.org/10.1248/CPB.51.948
1-Hydroxy-3-methoxy-2-methylanthracene-9,10-dione 10611938 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)OC 268.26 unknown https://doi.org/10.1248/CPB.51.948
1-Hydroxy-3-methoxyanthracene-9,10-dione 13412786 Click to see COC1=CC2=C(C(=C1)O)C(=O)C3=CC=CC=C3C2=O 254.24 unknown https://doi.org/10.1002/CHIN.200403232
https://doi.org/10.1248/CPB.51.948
1-Hydroxy-5-methoxy-2-methylanthracene-9,10-dione 13970503 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC=C3OC)O 268.26 unknown https://doi.org/10.1248/CPB.51.948
1,8-Dihydroxy-2-methylanthraquinone 11253808 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C(=CC=C3)O)O 254.24 unknown https://doi.org/10.1248/CPB.51.948
Anthraquinone base + 2O, MeOH, O-Hex-Pen 21917783 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)C(=O)C5=CC=CC=C5C4=O)O)CO)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1248/CPB.51.948
Digiferruginol 32209 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)CO)O 254.24 unknown https://doi.org/10.1248/CPB.51.948
Lucidin primeveroside 160180 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)C(=O)C5=CC=CC=C5C4=O)O)CO)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1248/CPB.51.948
https://doi.org/10.1002/CHIN.200403232
Rubiadinprimeveroside 213463 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 548.50 unknown https://doi.org/10.1002/CHIN.200403232
https://doi.org/10.1248/CPB.51.948
Rubiawallin A 85951330 Click to see COC1=CC2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3O)OC 284.26 unknown https://doi.org/10.1248/CPB.51.948
Rubiawallin B 10945434 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=C(C=C3)OC)O 268.26 unknown https://doi.org/10.1248/CPB.51.948
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
[6-(4,7-Dihydroxy-3-methyl-9,10-dioxoanthracen-2-yl)oxy-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl acetate 14539982 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C(=C4C(=C3)C(=O)C5=C(C4=O)C=CC(=C5)O)O)C)COC(=O)C)O)O)O)O)O 620.60 unknown https://doi.org/10.1248/CPB.51.948
1,2-Dihydroxy-3-methoxy-4-methylanthracene-9,10-dione 163192670 Click to see CC1=C2C(=C(C(=C1OC)O)O)C(=O)C3=CC=CC=C3C2=O 284.26 unknown https://doi.org/10.1002/CHIN.200403232
1,2-Dihydroxy-3-methylanthraquinone 429241 Click to see CC1=CC2=C(C(=C1O)O)C(=O)C3=CC=CC=C3C2=O 254.24 unknown https://doi.org/10.1002/CHIN.200403232
1,3-Dihydroxyanthraquinone 196978 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC(=C3)O)O 240.21 unknown https://doi.org/10.1002/CHIN.200403232
https://doi.org/10.1248/CPB.51.948
1,3-Dimethoxy-2-hydroxy-9,10-anthraquinone 15118825 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3C2=O)OC)O 284.26 unknown https://doi.org/10.1248/CPB.51.948
1,3,6-trihydroxy-2-methyl-9,10-anthraquinone-3-O-(6'-O-acetyl)-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 70698136 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C(=C4C(=C3)C(=O)C5=C(C4=O)C=CC(=C5)O)O)C)COC(=O)C)O)O)O)O)O 620.60 unknown https://doi.org/10.1248/CPB.51.948
1,3,6-trihydroxy-2-methyl-9,10-anthraquinone-3-O-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranoside 57335470 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C(=C4C(=C3)C(=O)C5=C(C4=O)C=CC(=C5)O)O)C)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1248/CPB.51.948
1,3,6-Trihydroxy-2-methylanthracene-9,10-dione 5319801 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=C(C2=O)C=C(C=C3)O)O 270.24 unknown https://doi.org/10.1021/NP2002918
https://doi.org/10.1248/CPB.51.948
2-(Methoxymethyl)-1,3-dihydroxyanthraquinone 149782 Click to see COCC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 284.26 unknown https://doi.org/10.1248/CPB.51.948
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-1,6-dihydroxy-2-methylanthracene-9,10-dione 14539977 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C(=C4C(=C3)C(=O)C5=C(C4=O)C=CC(=C5)O)O)C)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1248/CPB.51.948
Alizarin 1-methyl ether 80309 Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown https://doi.org/10.1002/CHIN.200403232
https://doi.org/10.1248/CPB.51.948
Lucidin 10163 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)CO)O 270.24 unknown https://doi.org/10.1002/CHIN.200403232
https://doi.org/10.1248/CPB.51.948
Nordamnacanthal 160712 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)C=O)O 268.22 unknown https://doi.org/10.1248/CPB.51.948
Purpurin 6683 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3O)O)O 256.21 unknown https://doi.org/10.1248/CPB.51.948
https://doi.org/10.1002/CHIN.200403232
Rubiadin 124062 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown https://doi.org/10.1248/CPB.51.948
https://doi.org/10.1016/J.JPHOTOBIOL.2010.09.009
https://doi.org/10.1002/CHIN.200403232
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Aminobenzoic acids and derivatives / Aminobenzoic acids
2-((Carboxymethyl)amino)-4-chlorobenzoic acid 11107141 Click to see C1=CC(=C(C=C1Cl)NCC(=O)O)C(=O)O 229.62 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
1,2-Benzenedi(carboxylic-14C)acid, dibutyl ester 171810 Click to see CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC 282.33 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[3-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 4546425 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC 388.40 unknown https://doi.org/10.1002/CHIN.200403232
https://doi.org/10.1248/CPB.51.948
Medioresinol 181681 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC 388.40 unknown https://doi.org/10.1248/CPB.51.948
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see CCCCCCCCCCCC(=O)O 200.32 unknown https://doi.org/10.1248/CPB.51.948
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.1002/CHIN.200403232
https://doi.org/10.1248/CPB.51.948
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45358157 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1248/CPB.51.948
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1248/CPB.51.948
https://doi.org/10.1002/CHIN.200403232
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17R)-17-[(E,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-3,10,13-trimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene 50930798 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)C)C)C)C(C)C 410.70 unknown via CMAUP database
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/CPB.51.948
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP020038K
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/10.1248/CPB.51.948
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/10.1002/CHIN.200403232
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/10.1248/CPB.51.948
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Stigmasta-5,22-dien-3beta-yl alpha-D-glucopyranoside 101689889 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown via CMAUP database
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/10.1021/NP020038K
https://doi.org/10.1002/CHIN.200403232
https://doi.org/10.1248/CPB.51.948
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Maltol 8369 Click to see CC1=C(C(=O)C=CO1)O 126.11 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1248/CPB.51.948
https://doi.org/10.1002/CHIN.200403232
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-6-methoxy-8-(3-methylbut-1-enyl)chromen-2-one 162876382 Click to see CC(C)C=CC1=C2C(=CC(=C1O)OC)C=CC(=O)O2 260.28 unknown https://doi.org/10.1002/CHIN.200403232
https://doi.org/10.1248/CPB.51.948
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1002/CHIN.200403232
https://doi.org/10.1248/CPB.51.948
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
[(4S,12R,15S,16S)-14,14-dimethyl-6-oxo-4-phenyl-3,11,13-trioxatetracyclo[8.6.0.02,7.012,16]hexadeca-1(10),2(7),8-trien-15-yl] acetate 42607797 Click to see CC(=O)OC1C2C(OC3=C2C4=C(C=C3)C(=O)CC(O4)C5=CC=CC=C5)OC1(C)C 394.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate(1-) 25201972 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)[O-] 285.23 unknown via CMAUP database
Apigenin-7-olate 25200950 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)[O-])O 269.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-3-methyl-3,4-dihydro-2H-chromene-5,7-diol 44445800 Click to see CC1CC2=C(C=C(C=C2OC1C3=CC(=C(C=C3)O)O)O)O 288.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
5-Hydroxy-3-(4-hydroxyphenyl)-8-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13965469 Click to see COC1=C(C=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.51.948

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