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Vatica affinis

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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 UUID643ffb29a2fd6120934158
Scientific name Vatica affinis
Authority Thwaites
First published in Enum. Pl. Zeyl. : 404 (1864)

Description Top

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Vatica affinis is a plant species belonging to the Dipterocarpaceae family and found exclusively in Sri Lanka. This species is currently classified as Critically Endangered due to the loss of its natural habitat.

Synonyms Top

No known synonyms.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000423153
KEW urn:lsid:ipni.org:names:321584-1
Open Tree Of Life 168386
NCBI Taxonomy 365571
IUCN Red List 30840
IPNI 321584-1
iNaturalist 182268
GBIF 5669249
Freebase /m/02y_zdk
Wikipedia Vatica_affinis

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
Chemistry and Biology of Resveratrol-Derived Natural Products Keylor MH, Matsuura BS, Stephenson CR Chem Rev 02-Apr-2015
PMCID:PMC4566929
doi:10.1021/cr500689b
PMID:25835567
Leveraging biodiversity knowledge for potential phyto-therapeutic applications Sharma V, Sarkar IN J Am Med Inform Assoc 21-Mar-2013
PMCID:PMC3721164
doi:10.1136/amiajnl-2012-001445
PMID:23518859
Polyphenols from dipterocarp species. Vaticaffinol and ε-viniferin Subramaniam Sotheeswaran, M. Uvais S. Sultanbawa, Sivagnanasundram Surendrakumar, Sinnathamby Balasubramaniam, Peter Bladon Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19850000159
Novel resveratrol tetramer, vaticaffinol, from Vatica affinis Thw. (dipterocarpaceae) M. Uvais S. Sultanbawa, Sivaguanasundram Surendrakumar, Mohamed I. M. Wazeer, Peter Bladon Royal Society of Chemistry (RSC) 30-Mar-2004
doi:10.1039/C39810001204
Three hydroxy ellagic acid methyl ethers, chrysophanol and scopoletin from Shorea worthingtonii and Vatica obscura Y.A. Geevananda, P. Gunawardana, N.Savitri Kumar, M.Uvais S. Sultanbawa Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)91468-7

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
(2R,3R,4S,4aR,10bR)-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one 6543710 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)O)O)OC2=O)O 328.27 unknown https://doi.org/10.1039/P19850000159
3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one 2356 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)O)O)OC2=O)O 328.27 unknown https://doi.org/10.1039/P19850000159
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Acetylursolic acid 619164 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1016/S0031-9422(00)91468-7
Ursolic acid acetate 6475119 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1016/S0031-9422(00)91468-7
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3R,10S,11S,18S,19R,26R,27R)-3,11,19,27-tetrakis(4-hydroxyphenyl)-12,28-dioxaoctacyclo[24.6.1.110,13.02,18.04,9.020,25.029,33.017,34]tetratriaconta-1(33),4(9),5,7,13,15,17(34),20(25),21,23,29,31-dodecaene-5,7,15,21,23,31-hexol 71566774 Click to see C1=CC(=CC=C1C2C3C(C(C4=C(C=C(C=C4O)O)C5C(OC6=CC(=CC3=C56)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=C1C(C(OC1=CC(=C9)O)C1=CC=C(C=C1)O)C1=C2C(=CC(=C1)O)O)O 906.90 unknown https://doi.org/10.1039/C39810001204
https://doi.org/10.1039/P19850000159
5-[(2R,3S)-6-hydroxy-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 5315234 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1039/P19850000159
5-[(2S,3R)-6-hydroxy-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dimethyl-1-benzofuran-3-yl]benzene-1,3-diol 163190492 Click to see CC1(C(C2=C(C=C(C=C2O1)O)C=CC3=CC=C(C=C3)O)(C)C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)O 482.50 unknown https://doi.org/10.1039/C39810001204
5-[6-Hydroxy-2-(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 366354 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1039/P19850000159
5-[6-Hydroxy-2-(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-2,3-dimethyl-1-benzofuran-3-yl]benzene-1,3-diol 162929294 Click to see CC1(C(C2=C(C=C(C=C2O1)O)C=CC3=CC=C(C=C3)O)(C)C4=CC(=CC(=C4)O)O)C5=CC=C(C=C5)O 482.50 unknown https://doi.org/10.1039/C39810001204
> Phenylpropanoids and polyketides / Coumarins and derivatives
5,7,13,14-Tetramethoxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione 162992818 Click to see COC1=CC(=C2C3=C1C(=O)OC4=C3C(=CC(=C4OC)OC)C(=O)O2)OC 358.30 unknown https://doi.org/10.1016/S0031-9422(00)91468-7
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
8-[5-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)-2-hydroxyphenyl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 162865148 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)C4=C5C(=C(C=C4O)O)C(=O)CC(O5)C6=CC(=C(C=C6)O)O 558.50 unknown https://doi.org/10.1039/C39810001204
https://doi.org/10.1039/P19850000159

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