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Aglaia crassinervia

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 UUID6440080e5c4b8448863431
Scientific name Aglaia crassinervia
Authority Kurz ex Hiern
First published in Fl. Brit. India 1: 556 (1875)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Aglaia cinerea King J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 64: 66 (1895)
Aglaia pyricarpa Baker f. J. Bot. 62(Suppl.): 20 (1924)
Chisocheton sumatranus Baker f. J. Bot. 62(Suppl.): 18 (1924)

Common names Top

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Language Common/alternative name
Vietnamese gội gân mập

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
  • Asia-tropical
    • Indo-China
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Malaya
      • Philippines
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000524010
Tropicos 100285040
KEW urn:lsid:ipni.org:names:577033-1
The Plant List kew-2626249
Open Tree Of Life 627542
NCBI Taxonomy 306497
IUCN Red List 34752
IPNI 577033-1
iNaturalist 189018
GBIF 5597818
Freebase /m/02x7pqc
Wikipedia Aglaia_crassinervia

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
Antitumor Profile of Carbon-Bridged Steroids (CBS) and Triterpenoids Dembitsky VM, Gloriozova TA, Poroikov VV Mar Drugs 03-Jun-2021
PMCID:PMC8228860
doi:10.3390/md19060324
PMID:34205074
Rocaglamide, Silvestrol and Structurally Related Bioactive Compounds from Aglaia Species Pan L, Woodard JL, Lucas DM, Fuchs JR, Kinghorn AD Nat Prod Rep 02-May-2014
PMCID:PMC4091845
doi:10.1039/c4np00006d
PMID:24788392
Bioactive Flavaglines and Other Constituents Isolated from Aglaia perviridis Pan L, Acuña UM, Li J, Jena N, Ninh TN, Pannell CM, Chai H, Fuchs JR, Carcache de Blanco EJ, Soejarto DD, Kinghorn AD J Nat Prod 09-Jan-2013
PMCID:PMC3606667
doi:10.1021/np3007588
PMID:23301897
The Relevance of Higher Plants in Lead Compound Discovery Programs Kinghorn AD, Pan L, Fletcher JN, Chai H J Nat Prod 08-Jun-2011
PMCID:PMC3158731
doi:10.1021/np200391c
PMID:21650152
Cabraleahy­droxy­lactone from the leaves of Aglaia exima Loong XM, Mohamad K, Awang K, A. Hadi AH, Ng SW Acta Crystallogr Sect E Struct Rep Online 11-Sep-2010
PMCID:PMC2983197
doi:10.1107/S1600536810035208
PMID:21587531
Potential of Plant-Derived Natural Products in the Treatment of Leukemia and Lymphoma Lucas DM, Still PC, Pérez LB, Grever MR, Kinghorn AD Curr Drug Targets 01-Jul-2010
PMCID:PMC2892601
doi:10.2174/138945010791320809
PMID:20370646
Natural Products as Aromatase Inhibitors Balunas MJ, Su B, Brueggemeier RW, Kinghorn AD Anticancer Agents Med Chem 01-Aug-2008
PMCID:PMC3074486
PMID:18690828
Activity-guided isolation of cytotoxic constituents from the bark of Aglaia crassinervia collected in Indonesia. Su BN, Chai H, Mi Q, Riswan S, Kardono LB, Afriastini JJ, Santarsiero BD, Mesecar AD, Farnsworth NR, Cordell GA, Swanson SM, Kinghorn AD Bioorg Med Chem 15-Feb-2006
doi:10.1016/J.BMC.2005.09.012
PMID:16216518

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
(1S,2R,3R,5R,10R,11R,14R,15S)-3-hydroxy-15-[(3S,5R,6R)-5-hydroxy-6-(2-hydroxypropan-2-yl)oxan-3-yl]-2,6,6,10-tetramethylpentacyclo[12.3.1.01,14.02,11.05,10]octadecan-7-one 163092630 Click to see CC1(C2CC(C3(C(C2(CCC1=O)C)CCC45C3(C4)CCC5C6CC(C(OC6)C(C)(C)O)O)C)O)C 488.70 unknown https://doi.org/10.1016/J.BMC.2005.09.012
(5S)-5-[(3R,5R,8R,9R,10R,13S,14R,17R)-3-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-5-methyloxolan-2-one 163010760 Click to see 416.60 unknown https://doi.org/10.1016/J.BMC.2005.09.012
(5S)-5-[(3S,5R,8R,9R,10R,13S,14R,17R)-3-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-5-methyloxolan-2-one 163010763 Click to see 416.60 unknown https://doi.org/10.1016/J.BMC.2005.09.012
[(4aS,6aS,6aS,6bR,8aR,10R,12aR,14bS)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4a-yl]methyl acetate 162917261 Click to see 526.80 unknown https://doi.org/10.1016/J.BMC.2005.09.012
3-Hydroxy-15-[5-hydroxy-6-(2-hydroxypropan-2-yl)oxan-3-yl]-2,6,6,10-tetramethylpentacyclo[12.3.1.01,14.02,11.05,10]octadecan-7-one 163092629 Click to see 488.70 unknown https://doi.org/10.1016/J.BMC.2005.09.012
3alpha,20-Dihydroxy-4,4,14-trimethyl-18-nor-5alpha-cholan-24-oic acid gamma-lactone 124222253 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C5(CCC(=O)O5)C)C)C)C 416.60 unknown https://doi.org/10.1016/J.BMC.2005.09.012
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(1S,2R,3R,5R,7S,10S,11R,14R,15S)-15-[(2R,3S,5R)-5-[(2R)-3,3-dimethyloxiran-2-yl]-2-hydroxyoxolan-3-yl]-3-hydroxy-2,6,6,10-tetramethyl-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] (E)-2-methylbut-2-enoate 163028972 Click to see 570.80 unknown https://doi.org/10.1016/J.BMC.2005.09.012
[(1S,2R,3R,5R,7S,10S,11R,14R,15S)-15-[(2S,3S,5R)-5-[(1R)-1,2-dihydroxy-2-methylpropyl]-2-hydroxyoxolan-3-yl]-3-hydroxy-2,6,6,10-tetramethyl-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] (E)-2-methylbut-2-enoate 162878482 Click to see 588.80 unknown https://doi.org/10.1016/J.BMC.2005.09.012
[15-[5-(1,2-Dihydroxy-2-methylpropyl)-2-hydroxyoxolan-3-yl]-3-hydroxy-2,6,6,10-tetramethyl-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] 2-methylbut-2-enoate 73150603 Click to see 588.80 unknown https://doi.org/10.1016/J.BMC.2005.09.012
[15-[5-(3,3-Dimethyloxiran-2-yl)-2-hydroxyoxolan-3-yl]-3-hydroxy-2,6,6,10-tetramethyl-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] 2-methylbut-2-enoate 73150602 Click to see 570.80 unknown https://doi.org/10.1016/J.BMC.2005.09.012
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
(2S,3R,5S,8R,9S,10S,13S,14S,17Z)-17-ethylidene-2,3-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-16-one 15427647 Click to see 332.50 unknown https://doi.org/10.1016/J.BMC.2005.09.012
> Organoheterocyclic compounds / Benzofurans / Flavaglines
Ferrugin 5089 Click to see 434.50 unknown https://doi.org/10.1016/J.BMC.2005.09.012
Rocaglaol 393602 Click to see 434.50 unknown https://doi.org/10.1016/J.BMC.2005.09.012
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1016/J.BMC.2005.09.012

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