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Lithocarpus irwinii

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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 UUID643fe1adbd489606840491
Scientific name Lithocarpus irwinii
Authority Rehder
First published in J. Arnold Arbor. 1: 127 (1919)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lithocarpus amygdalifolius var. praecipitorum Chun Acta Phytotax. Sin. 10: 208. 1965
Quercus irwinii Hance Ann. Sci. Nat., Bot. , sér. 4, 18: 229 (1862)
Pasania irwinii Oerst. Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1866: 83 (1866)
Synaedrys irwinii Koidz. Bot. Mag. (Tokyo) 30: 195 (1916)

Common names Top

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Language Common/alternative name
Chinese 广南柯
Chinese 港柯

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-0000229986
Tropicos 13100845
KEW urn:lsid:ipni.org:names:358804-1
The Plant List kew-114538
Open Tree Of Life 3930361
IPNI 358804-1
iNaturalist 739699
GBIF 5332318
EOL 1155737

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
Triterpenoids from ten Lithocarpus species of Hong Kong Wai Haan Hui, Phyllis D.S. Ko, Yuk-Chun Lee, Man-Moon Li, Henry R. Arthur Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(75)85187-9

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
(4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicene-2,3-dione 15081673 Click to see CC1C(=O)C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(75)85187-9
4,4,6a,6b,8a,12,14b-Heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol 610148 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1016/0031-9422(75)85187-9
4,4a,6a,6b,8a,11,11,14a-Octamethyl-1,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicene-2,3-dione 17815305 Click to see CC1C(=O)C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(75)85187-9
Taraxasterol 115250 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1016/0031-9422(75)85187-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(Z,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 163082003 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(75)85187-9
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(75)85187-9

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