Crepidiastrum chelidoniifolium

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Internal ID UUID643fcc8b4502f546879630
Scientific name Crepidiastrum chelidoniifolium
Authority (Makino) Pak & Kawano
First published in Mem. Fac. Sci. Kyoto Univ., Ser. Biol. , n.s., 15(1-2): 56 (1992)

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Synonyms Top

Scientific name Authority First published in
Paraixeris chelidoniifolia (Makino) Nakai Bot. Mag. (Tokyo) 34: 156 (1920)
Crepidiastrum koidzumianum (Kitam.) Pak & Kawano Mem. Fac. Sci. Kyoto Univ., Ser. Biol. , n.s., 15(1-2): 57 (1992)
Paraixeris koidzumiana (Kitam.) Tzvelev Fl. URSS xxix. 400 (1964), in obs.
Paraixeris saxatilis (A.I.Baranov) Tzvelev Fl. URSS 29: 400 (1964)
Youngia chelidoniifolia (Makino) Kitam. Acta Phytotax. Geobot. 11: 128 (1942)
Lactuca chelidoniifolia Makino Bot. Mag. (Tokyo) 12: 47 (1898)
Youngia koidzumiana Kitam. Acta Phytotax. Geobot. 11: 127 (1942)
Ixeris saxatilis (A.I.Baranov) Soják Novit. Bot. Delect. Seminum Horti Bot. Univ. Carol. Prag. 1962: 50 (1962) (1962)
Ixeris chelidoniifolia (Makino) Stebbins J. Bot. 75: 46 (1937)
Crepidiastrum saxatile (A.I.Baranov) Pak & Kawano Mem. Fac. Sci. Kyoto Univ., Ser. Biol. , n.s., 15(1-2): 57 (1992)
Lactuca saxatilis A.I.Baranov Zap. Kharbin. Obshch. Estestvoisp. Etnogr. 12: 34. 1954

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Language Common/alternative name
Korean 까치고들빼기
Chinese 少花黄瓜菜

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Primorye

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000063836
Tropicos 50117860
KEW urn:lsid:ipni.org:names:1117225-2
The Plant List gcc-20801
IPNI 1117225-2
iNaturalist 938903
GBIF 3145167
EOL 5112114

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
The inhibition of diacylglycerol acyltransferase by terpenoids from Youngia koidzumiana. Dat NT, Cai XF, Rho MC, Lee HS, Bae K, Kim YH Arch Pharm Res 01-Feb-2005
doi:10.1007/BF02977708
PMID:15789744

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
1-Nonadecanol 80281 Click to see CCCCCCCCCCCCCCCCCCCO 284.50 unknown https://doi.org/10.1007/BF02977708
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1007/BF02977708
Methyl Ursolate 636516 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown https://doi.org/10.1007/BF02977708
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1007/BF02977708
Ursolic acid methyl ester 89432794 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown https://doi.org/10.1007/BF02977708
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1007/BF02977708
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/10.1007/BF02977708
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-hydroxy-3,6-dimethyl-9-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3a,4,5,7,9a,9b-hexahydro-3H-azuleno[4,5-b]furan-2-one 162966621 Click to see CC1C2C(CC(=C3CC=C(C3C2OC1=O)COC4C(C(C(C(O4)CO)O)O)O)C)O 426.50 unknown https://doi.org/10.1007/BF02977708

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