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Garcinia thwaitesii

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64401d4127909069219870
Scientific name Garcinia thwaitesii
Authority Pierre
First published in Fl. Forest. Cochinch. 5: 4 (1883)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Garcinia ovalifolia var. acutifolia Hook.f. Fl. Brit. India 1: 269 (1874)
Garcinia spicata var. acutifolia (Hook.f.) Vesque Monogr. Phan. 8: 311 (1893)

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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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-0000694691
Tropicos 100340603
KEW urn:lsid:ipni.org:names:428271-1
Open Tree Of Life 6099900
IUCN Red List 30794
IPNI 428271-1
iNaturalist 192569
GBIF 3712495
Freebase /m/02w0ftf
Elurikkus 400621
Wikipedia Garcinia_thwaitesii

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
2,5-dihydroxy-1,6-dimethoxyxanthone and biflavonoids of Garcinia thwaitesii A.A.Leslie Gunatilaka, H.T.Badra Sriyani, Subramaniam Sotheeswaran, Eric S. Waight Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80096-5

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
(3S,10S,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 91744939 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
(3S,4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 40469639 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
(3S,5S,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 40469707 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
Lanosta-8,24-dien-3-ol 856 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
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/10.1016/S0031-9422(00)80096-5
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
2,5-Dihydroxy-1,6-dimethoxyxanthen-9-one 163037850 Click to see 288.25 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3R)-8-[(2S,3S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 162994926 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C5C(=C(C=C4O)O)C(=O)C(C(O5)C6=CC=C(C=C6)O)O)O 558.50 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
(2S,3S)-8-[(2S,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 163086230 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C5C(=C(C=C4O)O)C(=O)C(C(O5)C6=CC(=C(C=C6)O)O)O)O 574.50 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
(2S)-8-[(2R,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 162925605 Click to see 558.50 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
(2S)-8-[(2R,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 162971251 Click to see 542.50 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
[3,8'-Bi-4H-1-benzopyran]-4,4'-dione, 2,2',3,3'-tetrahydro-3',5,5',7,7'-pentahydroxy-2,2'-bis(4-hydroxyphenyl)-, (2S,2'R,3R,3'R)- 5317534 Click to see 558.50 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
8-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 15307520 Click to see 542.50 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
8-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-chroman-3-yl]-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-chroman-4-one 501506 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C5C(=C(C=C4O)O)C(=O)C(C(O5)C6=CC(=C(C=C6)O)O)O)O 574.50 unknown https://doi.org/10.1016/S0031-9422(00)80096-5
Dihydromorelloflavone 11467081 Click to see 558.50 unknown https://doi.org/10.1016/S0031-9422(00)80096-5

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