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Vepris bilocularis

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 UUID643ffaaa8a7f0182191492
Scientific name Vepris bilocularis
Authority Engl.
First published in Nat. Pflanzenfam. 3(4): 178 (1896)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Toddalia bilocularis Wight & Arn. Prodr. Fl. Ind. Orient. : 149 (1834)
Cranzia bilocularis Kuntze Revis. Gen. Pl. 1: 99 (1891)
Dipetalum biloculare Dalzell Hooker's J. Bot. Kew Gard. Misc. 2: 38 (1850)

Common names Top

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Language Common/alternative name
Malayalam മൂത്താശ്ശാരി

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-0000420149
Tropicos 100431958
KEW urn:lsid:ipni.org:names:775476-1
Open Tree Of Life 6126647
IPNI 775476-1
iNaturalist 898983
GBIF 3834708
Wikipedia Vepris_bilocularis

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
Pyranoquinolones and acridones from Vepris bilocularis Günter Brader, Markus Bacher, Harald Greger, Otmar Hofer Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(95)00922-1
Structure of veprisone, a constituent of Vepris bilocularis. Govindachari TR, Joshi BS, Sundararajan VN Tetrahedron 01-Jan-1970
doi:10.1016/S0040-4020(01)98523-0
PMID:5879389

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 / Steroids and steroid derivatives / Steroid lactones
2-Descarboxy-2-(methoxycarbonyl)-19-deoxylimonoic acid 16,17-lactone 3646272 Click to see 486.60 unknown https://doi.org/10.1016/S0040-4020(01)98523-0
methyl 2-[(1R,2R,4S,7S,8S,11R,12R,13R,16R)-7-(furan-3-yl)-1,8,12,15,15-pentamethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-13-yl]acetate 21576498 Click to see 486.60 unknown https://doi.org/10.1016/S0040-4020(01)98523-0
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
1-Hydroxy-10-methyl-3-(3-methylbut-2-enoxy)acridin-9-one 101995297 Click to see CC(=CCOC1=CC2=C(C(=C1)O)C(=O)C3=CC=CC=C3N2C)C 309.40 unknown https://doi.org/10.1016/0031-9422(95)00922-1
1,2,3-Trimethoxy-10-methylacridin-9(10h)-one 261727 Click to see 299.32 unknown https://doi.org/10.1016/0031-9422(95)00922-1
Arborinine 5281832 Click to see CN1C2=CC=CC=C2C(=O)C3=C(C(=C(C=C31)OC)OC)O 285.29 unknown https://doi.org/10.1016/0031-9422(95)00922-1
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
2,2-dimethyl-8-(3-methylbut-2-enoxy)-6H-pyrano[3,2-c]quinolin-5-one 101995296 Click to see 311.40 unknown https://doi.org/10.1016/0031-9422(95)00922-1
2,2,6-Trimethyl-8-(3-methylbut-2-enoxy)pyrano[3,2-c]quinolin-5-one 13970990 Click to see 325.40 unknown https://doi.org/10.1016/0031-9422(95)00922-1
7-Methoxyflindersine 101995295 Click to see CC1(C=CC2=C(O1)C3=C(C=C(C=C3)OC)NC2=O)C 257.28 unknown https://doi.org/10.1016/0031-9422(95)00922-1
Haplamine 648601 Click to see 257.28 unknown https://doi.org/10.1016/0031-9422(95)00922-1

Gallery Top

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Collections Top

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