Calceolaria pinifolia - Unknown
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Internal ID UUID64400eb60c981144943867
Scientific name Calceolaria pinifolia
Authority Cav.
First published in Icon. 5: 26 (1799)

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Synonyms Top

Scientific name Authority First published in
Fagelia pinifolia (Cav.) Kuntze Revis. Gen. Pl. 2: 460 (1891)

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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
  • Southern America
    • Southern South America
      • Argentina Northwest
      • Chile Central
      • Chile North

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000579841
Tropicos 29200652
KEW urn:lsid:ipni.org:names:41564-2
The Plant List kew-2691487
Open Tree Of Life 144465
NCBI Taxonomy 240974
IPNI 41564-2
iNaturalist 806753
GBIF 7375121

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)!
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Title Authors Publication Released IDs
MarkerMiner 1.0: A new application for phylogenetic marker development using angiosperm transcriptomes Chamala S, GarcĂ­a N, Godden GT, Krishnakumar V, Jordon-Thaden IE, De Smet R, Barbazuk WB, Soltis DE, Soltis PS Appl Plant Sci 06-Apr-2015
PMCID:PMC4406834
doi:10.3732/apps.1400115
PMID:25909041
Labdane Diterpenes from Calceolaria densifolia Juan A. Garbarino, Aurora Molinari American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50084A006
Inhibitory effect of sterols from Ruprechtia triflora and diterpenes from Calceolaria pinnifolia on the growth of Mycobacterium tuberculosis. Woldemichael GM, Franzblau SG, Zhang F, Wang Y, Timmermann BN Planta Med 01-Jul-2003
doi:10.1055/S-2003-41109
PMID:12898418

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 / Prenol lipids / Diterpenoids
(1R,4aS,10aR)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 10017708 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1055/S-2003-41109
3-[[(1S,4aR)-7-isopropyl-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]methoxy]-3-oxo-propanoic acid 510089 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)COC(=O)CC(=O)O)C 372.50 unknown https://doi.org/10.1055/S-2003-41109
3-O-[[(1R,4aR,7R,10aS)-7-ethenyl-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthren-1-yl]methyl] 1-O-methyl propanedioate 639656 Click to see CC1(CCC2=C(C1)CCC3C2(CCCC3(C)COC(=O)CC(=O)OC)C)C=C 388.50 unknown https://doi.org/10.1055/S-2003-41109
Dehydroabietinol 15586718 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)CO)C 286.50 unknown https://doi.org/10.1055/S-2003-41109
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Epioleanolic acid 11869658 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/10.1055/S-2003-41109
https://doi.org/10.1021/NP50084A006
3Alpha-Hydroxyurs-12-En-28-Oic Acid 7163177 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1055/S-2003-41109
https://doi.org/10.1021/NP50084A006
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1055/S-2003-41109

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