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Trichilia hispida

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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 UUID6440493f643fd921058001
Scientific name Trichilia hispida
Authority T.D.Penn.
First published in Fl. Neotrop. Monogr. 28: 73 (1981)

Description Top

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Synonyms Top

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Common names Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
    • Western South America
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001083606
Tropicos 20400605
KEW urn:lsid:ipni.org:names:898953-1
The Plant List tro-20400605
Open Tree Of Life 6125025
NCBI Taxonomy 1640466
IUCN Red List 36096
IPNI 898953-1
iNaturalist 444432
GBIF 3850190
Freebase /m/02y_wkc
Wikipedia Trichilia_hispida

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
Constituents of Trichilia hispida (Meliaceae). 2. A new triterpenoid, hispidone, and bourjotinolone A Shivanand D. Jolad, Joseph J. Hoffmann, Jack R. Cole, Michael S. Tempesta, Robert B. Bates American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/JO01303A044
Constituents of Trichilia hispida (Meliaceae). 4. Hispidols A and B, two new tirucallane triterpenoids Shivanand D. Jolad, Joseph J. Hoffmann, Karl H. Schram, Jack R. Cole, Michael S. Tempesta, Robert B. Bates American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/JO00333A037
Limonoids from Trichilia hirta Diógenes A.G. Cortez, Paulo C. Vieira, João B. Fernandes, G.Fátima G.F. da Silva, A.Gilberto Ferreira Elsevier BV 18-Nov-2003
doi:10.1016/0031-9422(92)90048-U

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 / Triterpenoids
(13alpha,14beta,17alpha,20S,23R,24S)-21,24-Epoxy-23,25-dihydroxy-5alpha-lanost-7-en-3-one 73657077 Click to see CC1(C2CC=C3C(C2(CCC1=O)C)CCC4(C3(CCC4C5CC(C(OC5)C(C)(C)O)O)C)C)C 472.70 unknown https://doi.org/10.1021/JO01303A044
https://doi.org/10.1016/0031-9422(92)90048-U
(5S,9R,10R,13S,14S,17S)-17-[(3S,5R,6S)-5-hydroxy-6-(2-hydroxypropan-2-yl)oxan-3-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162954160 Click to see CC1(C2CC=C3C(C2(CCC1=O)C)CCC4(C3(CCC4C5CC(C(OC5)C(C)(C)O)O)C)C)C 472.70 unknown https://doi.org/10.1021/JO01303A044
(5S,9R,10R,13S,14S,17S)-17-[(3S,5R,6S)-5,6-dihydroxy-7,7-dimethyloxepan-3-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162959266 Click to see CC1(C2CC=C3C(C2(CCC1=O)C)CCC4(C3(CCC4C5CC(C(C(OC5)(C)C)O)O)C)C)C 472.70 unknown https://doi.org/10.1021/JO01303A044
17-(5,6-Dihydroxy-7,7-dimethyloxepan-3-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 73657229 Click to see CC1(C2CC=C3C(C2(CCC1=O)C)CCC4(C3(CCC4C5CC(C(C(OC5)(C)C)O)O)C)C)C 472.70 unknown https://doi.org/10.1021/JO01303A044
Bourjotinolone A 21603611 Click to see CC1(C2CC=C3C(C2(CCC1=O)C)CCC4(C3(CCC4C5CC(C(OC5)C(C)(C)O)O)C)C)C 472.70 unknown https://doi.org/10.1021/JO00333A037
Hispidol B 13967183 Click to see CC(CC(C(C(C)(C)O)O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 476.70 unknown https://doi.org/10.1021/JO00333A037
Hispidone 21603613 Click to see CC1(C2CC=C3C(C2(CCC1=O)C)CCC4(C3(CCC4C5CC(C(C(OC5)(C)C)O)O)C)C)C 472.70 unknown https://doi.org/10.1021/JO00333A037

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Collections Top

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