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Corydalis campulicarpa

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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 UUID644013915d020168430946
Scientific name Corydalis campulicarpa
Authority Hayata
First published in Icon. Pl. Formosan. 3: 15 (1913)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 弯果黄堇

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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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-0000622147
Tropicos 50002733
KEW urn:lsid:ipni.org:names:672117-1
Open Tree Of Life 6130315
IPNI 672117-1
GBIF 5531053
Elurikkus 538565

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)!
Title Authors Publication Released IDs
[Studies on the alkaloids of Formosan Corydalis species. I. Alkaloids of Corydalis campulicarpa Hayata]. Lu ST, Wang SJ, Su TL Yakugaku Zasshi 01-Jul-1971
doi:10.1248/YAKUSHI1947.91.7_778
PMID:5105485

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
(1R,21S)-16,17-dimethoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaen-21-ol 21587563 Click to see COC1=C(C2=C(C=C1)C(C3C4=CC5=C(C=C4CCN3C2)OCO5)O)OC 355.40 unknown https://doi.org/10.1248/YAKUSHI1947.91.7_778
13-Berbinol, 9,10-dimethoxy-2,3-(methylenedioxy)- 10164 Click to see COC1=C(C2=C(C=C1)C(C3C4=CC5=C(C=C4CCN3C2)OCO5)O)OC 355.40 unknown https://doi.org/10.1248/YAKUSHI1947.91.7_778
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine 98570 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C(=C(C=C4)OC)OC)OCO3 369.40 unknown https://doi.org/10.1248/YAKUSHI1947.91.7_778
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown https://doi.org/10.1248/YAKUSHI1947.91.7_778

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