Coptis quinquefolia - Unknown
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Internal ID UUID6440134464999453339837
Scientific name Coptis quinquefolia
Authority Miq.
First published in Ann. Mus. Bot. Lugduno-Batavi 3: 7 (1867)

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Synonyms Top

Scientific name Authority First published in
Coptis morii Hayata Icon. Pl. Formosan. 3: 9 (1913)
Coptis quinquefolia var. pedatoquinquefolia Koidz. Bot. Mag. (Tokyo) 37: 31 1923
Coptis quinquefolia f. ramosa Makino Bot. Mag. (Tokyo) 25: 227 1911
Coptis quinquefolia var. ramosa (Makino) Ohwi Bull. Natl. Sci. Mus. Tokyo 33: 72 1953
Coptis ramosa (Makino) Tamura Acta Phytotax. Geobot. 17: 118 (1958)

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Language Common/alternative name
Japanese バイカオウレン
Chinese 五葉黃連
Chinese 臺灣黃連
Chinese 五叶黄连

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Varieties (abbr. var.) Top

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Name Authority First published in
Coptis quinquefolia var. shikokumontana Kadota J. Jap. Bot. 79: 316 (2004)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000619870
Tropicos 27100369
KEW urn:lsid:ipni.org:names:710323-1
The Plant List kew-2736126
Open Tree Of Life 830003
NCBI Taxonomy 261444
IPNI 710323-1
iNaturalist 702412
GBIF 7277301
EPPO CPXQU
EOL 2873647
USDA GRIN 423365

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
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
Jatrorrhizine: A Review of Sources, Pharmacology, Pharmacokinetics and Toxicity Zhong F, Chen Y, Chen J, Liao H, Li Y, Ma Y Front Pharmacol 13-Jan-2022
PMCID:PMC8793695
doi:10.3389/fphar.2021.783127
PMID:35095493
Protoberberine alkaloids from Fissistigma balansae Yi-Chen Chia, Fang-Rong Chang, Chao-Ming Li, Yang-Chang Wu Elsevier BV 23-Apr-2003
doi:10.1016/S0031-9422(97)00775-9

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 / Aporphines
Magnoflorine 73337 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C 342.40 unknown https://doi.org/10.1016/S0031-9422(97)00775-9
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberastine 442180 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4C(C3)O)OCO5)OC 352.40 unknown https://doi.org/10.1016/S0031-9422(97)00775-9
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown https://doi.org/10.1016/S0031-9422(97)00775-9
Columbamine 72310 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)O)OC 338.40 unknown https://doi.org/10.1016/S0031-9422(97)00775-9
Coptisine 72322 Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6 320.30 unknown https://doi.org/10.1016/S0031-9422(97)00775-9
Palmatine 19009 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)OC 352.40 unknown https://doi.org/10.1016/S0031-9422(97)00775-9
Thalifendine 3084288 Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)O 322.30 unknown https://doi.org/10.1016/S0031-9422(97)00775-9
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
16-Methoxy-6,8-dioxa-1-azapentacyclo[11.8.0.03,11.05,9.014,19]henicosa-2,4,9,11,13,15,18-heptaen-17-one 25050405 Click to see COC1=CC2=C3C=C4C=C5C(=CC4=CN3CCC2=CC1=O)OCO5 321.30 unknown https://doi.org/10.1016/S0031-9422(97)00775-9
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 10065647 Click to see COC1=C(C2=CN3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)OC)OC 337.40 unknown https://doi.org/10.1016/S0031-9422(97)00775-9

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