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Walsura trifoliolata

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 UUID643ffa48cf867667567988
Scientific name Walsura trifoliolata
Authority (A.Juss.) Harms
First published in Nat. Pflanzenfam. ed. 2 , 19b(1): 119 (1940)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Walsura piscidia Roxb. Fl. Ind. ed. 1832 , 2: 387 (1832)
Trichilia coriacea B.Heyne ex Wall. Numer. List : n.º 1265 (1829)
Heynea trifoliolata A.Juss. Bull. Sci. Nat. Géol. 23: 238 (1830)
Illigera obtusa Meisn. Prodr. 15(1): 251 (1864)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Walsura trifoliolata subsp. acuminata (Trimen) T.P.Clark Blumea 38: 265 (1994)
Walsura trifoliolata subsp. trifoliolata

Varieties (abbr. var.) Top

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Name Authority First published in
Walsura trifoliolata var. ternata (Roxb.) H.O.Saxena Fl. Orissa 1: 284 (1994)

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-0000418019
Tropicos 100425422
KEW urn:lsid:ipni.org:names:579951-1
Open Tree Of Life 5516732
NCBI Taxonomy 1437462
IPNI 579951-1
iNaturalist 981181
GBIF 7271382
USDA GRIN 467646
Wikipedia Walsura_trifoliolata
CMAUP NPO26224

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
Sharpless Asymmetric Dihydroxylation: An Impressive Gadget for the Synthesis of Natural Products: A Review Mushtaq A, Zahoor AF, Bilal M, Hussain SM, Irfan M, Akhtar R, Irfan A, Kotwica-Mojzych K, Mojzych M Molecules 17-Mar-2023
PMCID:PMC10051988
doi:10.3390/molecules28062722
PMID:36985698

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see 382.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Piscidinol A 12004524 Click to see 474.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Epoxyazadiradione 49863985 Click to see 466.60 unknown via CMAUP database
methyl (1S,2R,3S,4R,8R,9S,10R,13R,15R)-2-acetyloxy-13-(furan-3-yl)-9-(2-methoxy-2-oxoethyl)-4,8,10,12-tetramethyl-7-oxo-16-oxatetracyclo[8.6.0.03,8.011,15]hexadeca-5,11-diene-4-carboxylate 93473232 Click to see 540.60 unknown via CMAUP database
Nimbidic acid 185704 Click to see CC1=C2C(CC1C3=COC=C3)OC4C2(C(C5(C(CC(C6(C5C4OC6)C)O)O)C)CC(=O)O)C 458.50 unknown via CMAUP database
Nimbin 108058 Click to see 540.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database

Gallery Top

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Collections Top

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