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Corydalis heterocarpa

Corydalis heterocarpa - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644013a08f0a7815520127
Scientific name Corydalis heterocarpa
Authority Siebold & Zucc.
First published in Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 173 (1845)

Description Top

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Synonyms Top

Scientific name Authority First published in
Corydalis hirtipes B.U.Oh & J.G.Kim J. Pl. Biol. 45: 237 (2002)
Corydalis oldhamii Koidz. Bot. Mag. (Tokyo) 44: 107 (1930)

Common names Top

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Language Common/alternative name
Japanese 筑紫黄華鬘
Japanese ツクシキケマン
Chinese 巨紫堇
Chinese 异果黄堇

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Corydalis heterocarpa var. japonica (Franch. & Sav.) Ohwi Acta Phytotax. Geobot. 13: 181 1943

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Begin at 20°C for 6 weeks, cool to 4°C for 6 weeks, then gradually increase to 10°C over 6 weeks. If no germination, the cycle is repeated.
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.
reported to be a warm germinator like C. ochroleuca and lutea; self seeds

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000622434
Tropicos 24000043
KEW urn:lsid:ipni.org:names:672274-1
The Plant List kew-2738822
Open Tree Of Life 5727953
NCBI Taxonomy 1030656
IPNI 672274-1
iNaturalist 452147
GBIF 5531423
EPPO COYHE
EOL 5473594

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
Salt-Tolerant Plants, Halophytes, as Renewable Natural Resources for Cancer Prevention and Treatment: Roles of Phenolics and Flavonoids in Immunomodulation and Suppression of Oxidative Stress towards Cancer Management Mohammed HA, Emwas AH, Khan RA Int J Mol Sci 08-Mar-2023
PMCID:PMC10048981
doi:10.3390/ijms24065171
PMID:36982245
Libanoridin Isolated from Corydalis heterocarpa Inhibits Adipogenic Differentiation of Bone Marrow-Derived Mesenchymal Stromal Cells Karadeniz F, Oh JH, Jang MS, Seo Y, Kong CS Int J Mol Sci 23-Dec-2022
PMCID:PMC9820566
doi:10.3390/ijms24010254
PMID:36613696
Anticatabolic and Anti-Inflammatory Effects of Myricetin 3-O-β-d-Galactopyranoside in UVA-Irradiated Dermal Cells via Repression of MAPK/AP-1 and Activation of TGFβ/Smad Oh JH, Karadeniz F, Lee JI, Park SY, Seo Y, Kong CS Molecules 14-Mar-2020
PMCID:PMC7144112
doi:10.3390/molecules25061331
PMID:32183404
Screening of promising chemotherapeutic candidates from plants extracts Kinjo J, Nakano D, Fujioka T, Okabe H J Nat Med 16-Apr-2016
PMCID:PMC4935755
doi:10.1007/s11418-016-0992-2
PMID:27086008
Anti-Inflammatory Activity of Heterocarpin from the Salt Marsh Plant Corydalis heterocarpa in LPS-Induced RAW 264.7 Macrophage Cells Kim YA, Kong CS, Park HH, Lee E, Jang MS, Nam KH, Seo Y Molecules 10-Aug-2015
PMCID:PMC6332082
doi:10.3390/molecules200814474
PMID:26266403
Rhamnus davurica leaf extract inhibits Fyn activation by antigen in mast cells for anti-allergic activity Kim JH, Kim AR, Kim HS, Kim HW, Park YH, You JS, Park YM, Her E, Kim HS, Kim YM, Choi WS BMC Complement Altern Med 25-Mar-2015
PMCID:PMC4379541
doi:10.1186/s12906-015-0607-6
PMID:25887889
THE ALKALOIDS OF FUMARIACEOUS PLANTS: XXXV. <i>CORYDALIS PLATYCARPA</i> MAKINO Richard H. F. Manske Canadian Science Publishing 24-Apr-2011
doi:10.1139/CJR43B-002
Biotransformation of Phthalideisoquinoline Alkaloids by Corydalis Tissue Cultures Kinuko Iwasa, Miyoko Kamigauchi, Narao Takao Wiley 17-Oct-2006
doi:10.1002/ARDP.19873200805
Threatened Pollination Systems in Native Flora of the Ogasawara (Bonin) Islands ABE T Ann Bot 01-Aug-2006
PMCID:PMC2803473
doi:10.1093/aob/mcl117
PMID:16790463
[Studies on the alkaloids of fumariaces plants. XII. Alkaloids of Corydalis platycarpa Makino. 3. On the tertiary base]. Tani C, Imanishi I, Nishijo J Yakugaku Zasshi 01-Aug-1970
doi:10.1248/YAKUSHI1947.90.8_1028
PMID:5466157
[Studies on the alkaloids of Fumariaces plants. XI. Alkaloids of Corydalis platycarpa Makino. (2). Dehydrocapaurimine]. Tani C, Imanishi I, Nishijo J Yakugaku Zasshi 01-Jul-1970
doi:10.1248/YAKUSHI1947.90.7_903
PMID:5465405
[Studies on the alkaloids of fumariaceos plants. X. Alkaloids of Corydalis platycarpa Makino. I]. Tani C, Imanishi I, Nishijo J Yakugaku Zasshi 01-Mar-1970
doi:10.1248/YAKUSHI1947.90.3_407
PMID:5464177

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 / Phthalide isoquinolines
beta-Narcotine 31411 Click to see CN1CCC2=CC3=C(C(=C2C1C4C5=C(C(=C(C=C5)OC)OC)C(=O)O4)OC)OCO3 413.40 unknown https://doi.org/10.1002/ARDP.19873200805
Noscapine 275196 Click to see CN1CCC2=CC3=C(C(=C2C1C4C5=C(C(=C(C=C5)OC)OC)C(=O)O4)OC)OCO3 413.40 unknown https://doi.org/10.1002/ARDP.19873200805
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(+/-)-Isocorypalmine 10220 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown https://doi.org/10.1139/CJR43B-002
(13aS)-2,3,10-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-1,9-diol 12302410 Click to see COC1=C(C2=C(CC3C4=C(C(=C(C=C4CCN3C2)OC)OC)O)C=C1)O 357.40 unknown https://doi.org/10.1248/YAKUSHI1947.90.7_903
(1S,24S)-24-methyl-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.02,10.04,8.015,23.016,20]tetracosa-2,4(8),9,15(23),16(20),21-hexaene 162885455 Click to see CC1C2C3=CC4=C(C=C3CCN2CC5=C1C=CC6=C5OCO6)OCO4 337.40 unknown https://doi.org/10.1248/YAKUSHI1947.90.3_407
(S)-Cheilanthifoline 440582 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)O 325.40 unknown https://doi.org/10.1248/YAKUSHI1947.90.8_1028
(S)-Tetrahydrocolumbamine 440229 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown https://doi.org/10.1139/CJR43B-002
2,3,10-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-1,9-diol 12302408 Click to see COC1=C(C2=C(CC3C4=C(C(=C(C=C4CCN3C2)OC)OC)O)C=C1)O 357.40 unknown https://doi.org/10.1248/YAKUSHI1947.90.7_903
2,9,10-trimethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-3-ol 5316090 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)O)OC 355.40 unknown https://doi.org/10.1139/CJR43B-002
24-Methyl-5,7,17,19-tetraoxa-13-azahexacyclo[11.11.0.02,10.04,8.015,23.016,20]tetracosa-2,4(8),9,15(23),16(20),21-hexaene 5321847 Click to see CC1C2C3=CC4=C(C=C3CCN2CC5=C1C=CC6=C5OCO6)OCO4 337.40 unknown https://doi.org/10.1248/YAKUSHI1947.90.3_407
Chelianthifoline 5117621 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)O 325.40 unknown https://doi.org/10.1248/YAKUSHI1947.90.8_1028
Corybulbine 10316181 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)O)OC 355.40 unknown https://doi.org/10.1139/CJR43B-002
Corypalmine 185605 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)OC 341.40 unknown https://doi.org/10.1248/YAKUSHI1947.90.3_407
Discretinine 11186895 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)OC 341.40 unknown https://doi.org/10.1248/YAKUSHI1947.90.3_407
DL-Tetrahydropalmatine 5417 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown https://doi.org/10.1248/YAKUSHI1947.90.8_1028
https://doi.org/10.1248/YAKUSHI1947.90.3_407
Tetrahydropalmatine 72301 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown https://doi.org/10.1248/YAKUSHI1947.90.3_407
https://doi.org/10.1248/YAKUSHI1947.90.8_1028
> Alkaloids and derivatives / Protopine alkaloids
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/YAKUSHI1947.90.8_1028

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