Coptis trifolia - Unknown
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Details Top

Internal ID UUID64401344978c5648911113
Scientific name Coptis trifolia
Authority Salisb.
First published in Trans. Linn. Soc. London 8: 305 (1807)

Description Top

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Synonyms Top

Scientific name Authority First published in
Anemone groenlandica O.F.Müll. Fl. Dan. [Oeder] t. 566.
Anemone groenlandica Oeder Fl. Dan. 4(10): 5 (1771)
Chryza borealis Raf. Med. Repos. 5: 352 (1808)
Coptis daisetsuensis Tatew. ex Miyabe & Tatew. Trans. Sapporo Nat. Hist. Soc. xiv. 2 (1935), in syn.
Coptis groenlandica Fernald Rhodora 31: 142 (1929)
Coptis trifolia subsp. groenlandica (Oeder) Hultén Fl. Aleutian Isl. : 178 (1937)
Coptis trifolia var. groenlandica Fassett Trans. Wisconsin Acad. Sci. 38: 195 (1946)
Coptis trifolia var. semiplena Miyabe & Tatew. Trans. Sapporo Nat. Hist. Soc. 14: 2 1935
Helleborus pumilus Salisb. Prodr. Stirp. Chap. Allerton : 374 (1796)
Helleborus trifoliatus Houtt. Nat. Hist. 2(9): 262 (1778)
Helleborus trifolius L. Sp. Pl. : 558 (1753)
Helleborus trilobus Lam. Encycl. 3: 98 (1789)
Isopyrum trifolium Britton Bull. Torrey Bot. Club 18: 265 (1891)

Common names Top

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Language Common/alternative name
English threeleaf goldthread
Arabic كوبتس تريفوليا
Arabic عرق الذهب
Arabic كوبتس ثلاثي الورق
Arabic كوبتس غرونلاند
Arabic خيط الذهب
German dreiblättriger goldfaden
French coptide du groenland
French coptide trifoliée
French coptide trifoliolée
French savoyane
French sawayane
Japanese ミツバオウレン
pdc goldwatzel

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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Maintain seeds at a constant 10°C.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
hydrophilic, plant in peat based medium

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Eastern Asia
      • Japan
    • Russian Far East
      • Kamchatka
      • Khabarovsk
      • Kuril Islands
      • Magadan
      • Primorye
      • Sakhalin
    • Siberia
      • Yakutskiya
  • Northern America
    • Eastern Canada
      • Labrador
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Minnesota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Southeastern U.S.A.
      • District Of Columbia
      • Maryland
    • Subarctic America
      • Alaska
      • Aleutian Islands
      • Greenland
      • Northwest Territorie
      • Nunavut
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000619881
UNII JXD8M951VX
Canadensys 8471
USDA Plants COTR2
Tropicos 27100081
INPN 762066
KEW urn:lsid:ipni.org:names:710328-1
The Plant List kew-2736138
Open Tree Of Life 982768
Observations.org 148378
NCBI Taxonomy 38790
Nature Serve 2.154777
IPNI 710328-1
iNaturalist 126251
GBIF 3033632
Freebase /m/0gf3sc
WisFlora 3200
FEIS plants/forb/coptri
EPPO CPXTR
EOL 594145
USDA GRIN 402567
Wikipedia Coptis_trifolia
CMAUP NPO28627.1

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
Addressing the preventive and therapeutic perspective of berberine against diabetes Shrivastava S, Sharma A, Saxena N, Bhamra R, Kumar S Heliyon 03-Nov-2023
PMCID:PMC10663750
doi:10.1016/j.heliyon.2023.e21233
PMID:38027723
Coptisine Inhibits Influenza Virus Replication by Upregulating p21 He MF, Liang JH, Shen YN, Zhang CW, Yang KY, Liu LC, Xie Q, Hu C, Song X, Wang Y Molecules 14-Jul-2023
PMCID:PMC10386263
doi:10.3390/molecules28145398
PMID:37513270
Role of Fenugreek, Cinnamon, Curcuma longa, Berberine and Momordica charantia in Type 2 Diabetes Mellitus Treatment: A Review Cortez-Navarrete M, Pérez-Rubio KG, Escobedo-Gutiérrez MD Pharmaceuticals (Basel) 30-Mar-2023
PMCID:PMC10145167
doi:10.3390/ph16040515
PMID:37111272
Scale‐dependent effects of marine subsidies on the island biogeographic patterns of plants Obrist DS, Fitzpatrick OT, Brown NE, Hanly PJ, Nijland W, Reshitnyk LY, Wickham SB, Darimont CT, Reynolds JD, Starzomski BM Ecol Evol 09-Sep-2022
PMCID:PMC9461347
doi:10.1002/ece3.9270
PMID:36177118
Vascular Plants Flora of Mire Ecosystem of the Bolshoy Shantar Island (the Far East of Russia) Kuptsova VA, Antonova LA, Chakov VV Plants (Basel) 08-Mar-2022
PMCID:PMC8948750
doi:10.3390/plants11060723
PMID:35336605
Current Advances in Coptidis Rhizoma for Gastrointestinal and Other Cancers He L, Zhong Z, Chen M, Liang Q, Wang Y, Tan W Front Pharmacol 03-Jan-2022
PMCID:PMC8762280
doi:10.3389/fphar.2021.775084
PMID:35046810
Floristic Changes in the Understory Vegetation of Mixed Temperate New England Freshwater Island Forests over a Period of 33 Years Holland MM, Winkler M Plants (Basel) 18-Nov-2020
PMCID:PMC7698944
doi:10.3390/plants9111600
PMID:33218069
Vegetation changes in temperate ombrotrophic peatlands over a 35 year period Pinceloup N, Poulin M, Brice MH, Pellerin S PLoS One 13-Feb-2020
PMCID:PMC7018058
doi:10.1371/journal.pone.0229146
PMID:32053706
Rhizoma Coptidis and Berberine as a Natural Drug to Combat Aging and Aging-Related Diseases via Anti-Oxidation and AMPK Activation Xu Z, Feng W, Shen Q, Yu N, Yu K, Wang S, Chen Z, Shioda S, Guo Y Aging Dis 01-Dec-2017
PMCID:PMC5758350
doi:10.14336/AD.2016.0620
PMID:29344415
Correction: Long-Term Regional Shifts in Plant Community Composition Are Largely Explained by Local Deer Impact Experiments Frerker K, Sabo A, Waller D PLoS One 13-Sep-2017
PMCID:PMC5597238
doi:10.1371/journal.pone.0185037
PMID:28902901
The Mouthwash War - Chlorhexidine vs. Herbal Mouth Rinses: A Meta-Analysis Manipal S, Hussain S, Wadgave U, Duraiswamy P, Ravi K J Clin Diagn Res 01-May-2016
PMCID:PMC4948542
doi:10.7860/JCDR/2016/16578.7815
PMID:27437366
Beyond a Climate-Centric View of Plant Distribution: Edaphic Variables Add Value to Distribution Models Beauregard F, de Blois S PLoS One 21-Mar-2014
PMCID:PMC3962442
doi:10.1371/journal.pone.0092642
PMID:24658097
New reports of nuclear DNA content for 407 vascular plant taxa from the United States Bai C, Alverson WS, Follansbee A, Waller DM Ann Bot 24-Oct-2012
PMCID:PMC3503501
doi:10.1093/aob/mcs222
PMID:23100602
Post-Disturbance Plant Community Dynamics following a Rare Natural-Origin Fire in a Tsuga canadensis Forest Murray BD, Holmes SA, Webster CR, Witt JC PLoS One 21-Aug-2012
PMCID:PMC3424231
doi:10.1371/journal.pone.0043867
PMID:22928044
Flora and Vegetation of Tasiilaq, Formerly Angmagssalik, Southeast Greenland: A Comparison of Data Between Around 1900 and 2007 Daniëls FJ, de Molenaar JG Ambio 24-Aug-2011
PMCID:PMC3357867
doi:10.1007/s13280-011-0171-3
PMID:21954727

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
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Epiberberine 160876 Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC5=C(C4=C3)OCO5)OC 336.40 unknown https://doi.org/10.1016/0031-9422(92)90073-Y
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Catalpic acid 5385589 Click to see CCCCC=CC=CC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols / 1,2-diacyl-3-O-beta-D-galactosyl-sn-glycerols
[(2S)-2-[(9Z,12Z)-octadeca-9,12-dienoyl]oxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] (Z)-octadec-9-enoate 10509461 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC 781.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4bR,6R,7R,8aS)-2-ethenyl-1,6,7-trihydroxy-2,4b,8,8-tetramethyl-1,5,6,7,8a,9-hexahydrophenanthren-3-one 56954823 Click to see CC1(C2CC=C3C(C(C(=O)C=C3C2(CC(C1O)O)C)(C)C=C)O)C 332.40 unknown via CMAUP database
(1R,4S,6S,9S,10S,13S)-6-hydroxy-5,5,9,13-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-7,12-dione 5352023 Click to see CC1(C2CCC34CC(C=C3)(C(=O)CC4C2(CC(=O)C1O)C)C)C 316.40 unknown via CMAUP database
(5beta,10alpha,13R)-3alpha-Hydroxypimara-8(14),15-diene-12-one 101448906 Click to see CC1(C2CCC3=CC(C(=O)CC3C2(CCC1O)C)(C)C=C)C 302.50 unknown via CMAUP database
17-Norkaur-15-ene-3,12-dione, 13-methyl-, (8I(2),13I(2))- 100926172 Click to see CC1(C2CCC34CC(C=C3)(C(=O)CC4C2(CCC1=O)C)C)C 300.40 unknown via CMAUP database
Beyerene 107412 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C=C4)C)C)C 272.50 unknown via CMAUP database
Ent-pimara-8(14),15-diene 12314280 Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C 272.50 unknown via CMAUP database
yucalexin B-22 44448252 Click to see CC1(C2CCC34CC(C=C3)(C(=O)CC4C2(CC(C1O)O)C)C)C 318.40 unknown via CMAUP database
yucalexin P-15 44448251 Click to see CC1(C2CC=C3C(C(C(=O)C=C3C2(CC(=O)C1O)C)(C)C=C)O)C 330.40 unknown via CMAUP database
yucalexin P-17 44448241 Click to see CC1(C2CCC3=CC(C(CC3C2(CC(=O)C1O)C)O)(C)C=C)C 318.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
ent-Kaurene 11966109 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)C 272.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(16S)-16-Hydroxy-13,16-secotrachyloba-13-ene-3-one 100926173 Click to see CC1(C2CCC34CC(C(CC3C2(CCC1=O)C)C=C4)(C)O)C 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(2R,4aR,6aR,6bR,8aR,12aR,14aS,14bR)-2,4a,6b,9,9,12a,14a-heptamethyl-10-oxo-3,4,5,6a,7,8,8a,11,12,13,14,14b-dodecahydro-1H-picene-2-carboxylic acid 102134163 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4(C3=CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 454.70 unknown via CMAUP database
Isotaraxerol 12443227 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
Taraxerone 92785 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
7-[(2E,6Z)-3,7-dimethyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyocta-2,6-dienoxy]-6-methoxychromen-2-one 163188175 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)CCC=C(C)COC3C(C(C(C(O3)CO)O)O)O 506.50 unknown https://doi.org/10.1016/0031-9422(92)90073-Y
7-[(2E,6Z)-3,7-dimethyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxyocta-2,6-dienoxy]-6-methoxychromen-2-one 163188420 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC(=CCCC(=CCOC3=C(C=C4C=CC(=O)OC4=C3)OC)C)C)O)O)O)O)O)O 652.70 unknown https://doi.org/10.1016/0031-9422(92)90073-Y
7-[(2E,6Z)-3,7-dimethyl-8-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxyocta-2,6-dienoxy]-6-methoxychromen-2-one 163009914 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC(=CCCC(=CCOC3=C(C=C4C=CC(=O)OC4=C3)OC)C)C)O)O)O)O)O)O 652.70 unknown https://doi.org/10.1016/0031-9422(92)90073-Y
7-[(2E,6Z)-3,7-dimethyl-8-[(2R,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyocta-2,6-dienoxy]-6-methoxychromen-2-one 162882433 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)CCC=C(C)COC3C(C(C(C(O3)CO)O)O)O 506.50 unknown https://doi.org/10.1016/0031-9422(92)90073-Y
7-[3,7-Dimethyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyocta-2,6-dienoxy]-6-methoxychromen-2-one 162882432 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)CCC=C(C)COC3C(C(C(C(O3)CO)O)O)O 506.50 unknown https://doi.org/10.1016/0031-9422(92)90073-Y
7-[3,7-Dimethyl-8-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxyocta-2,6-dienoxy]-6-methoxychromen-2-one 163009912 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC(=CCCC(=CCOC3=C(C=C4C=CC(=O)OC4=C3)OC)C)C)O)O)O)O)O)O 652.70 unknown https://doi.org/10.1016/0031-9422(92)90073-Y
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 38359273 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown via CMAUP database
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 via CMAUP database
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown via CMAUP database
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14R,17R)-17-[(E,1R,4S)-4-ethyl-1,5-dimethyl-hex-2-enyl]-8,10,13-trimethyl-1,2,3,4,7,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 23246947 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2(CC=C4C3(CCC(C4)O)C)C)C)C(C)C 426.70 unknown via CMAUP database
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 12943207 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C)C(C)C 410.70 unknown via CMAUP database
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/10.1016/0031-9422(92)90073-Y
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/10.1016/0031-9422(92)90073-Y
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/10.1016/0031-9422(92)90073-Y
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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Epilotaustralin 185818 Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 261.27 unknown via CMAUP database
Linamarin 11128 Click to see CC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 247.24 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-((6-O-(beta-D-apiofuranosyl)beta-D-glucopyranosyl)oxy)propane 10316099 Click to see CC(C)OC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O 354.35 unknown via CMAUP database
ethyl beta-D-glucopyranoside 121667 Click to see CCOC1C(C(C(C(O1)CO)O)O)O 208.21 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
16-Methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one 11723579 Click to see COC1=CC2=C3C=C4C=CC5=C(C4=CN3CCC2=CC1=O)OCO5 321.30 unknown https://doi.org/10.1016/0031-9422(92)90073-Y
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/0031-9422(92)90073-Y
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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
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

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