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Internal ID UUID6440081336e96501388130
Scientific name Aglaia leptantha
Authority Miq.
First published in Ann. Mus. Bot. Lugduno-Batavi 4: 51 (1868)

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Synonyms Top

Scientific name Authority First published in
Aglaia annamensis Pellegr. Bull. Soc. Bot. France 91: 179 (1945)
Aglaia gamopetala Merr. Univ. Calif. Publ. Bot. 15: 126 (1929)
Aglaia glabriflora Hiern Fl. Brit. India 1: 555 (1875)
Aglaia glabrifolia Merr. Univ. Calif. Publ. Bot. 15: 129 (1929)
Aglaia laevigata Merr. Publ. Bur. Sci. Gov. Lab. 35: 31 (1906)

Common names Top

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Language Common/alternative name
Vietnamese gội trung bộ
Vietnamese ngâu trung bộ

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Varieties (abbr. var.) 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
  • Asia-tropical
    • Indo-China
      • Cambodia
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000524172
Tropicos 50094801
KEW urn:lsid:ipni.org:names:577166-1
The Plant List kew-2626398
Open Tree Of Life 5516760
NCBI Taxonomy 1472161
IUCN Red List 34672
IPNI 577166-1
iNaturalist 189045
GBIF 5597522
Freebase /m/02x7q6w
Wikipedia Aglaia_leptantha

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
Exploring the Potential of Phytocompounds for Targeting Epigenetic Mechanisms in Rheumatoid Arthritis: An In Silico Study Using Similarity Indexing Deshpande SH, Bagewadi ZK, Khan TM, Mahnashi MH, Shaikh IA, Alshehery S, Khan AA, Patil VS, Roy S Molecules 07-Mar-2023
PMCID:PMC10051859
doi:10.3390/molecules28062430
PMID:36985402
Update on Phytochemical and Biological Studies on Rocaglate Derivatives from Aglaia Species Agarwal G, Chang LS, Soejarto DD, Kinghorn AD Planta Med 30-Mar-2021
PMCID:PMC8481333
doi:10.1055/a-1401-9562
PMID:33784769
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
Discovery of new anticancer agents from higher plants Pan L, Chai HB, Kinghorn AD Front Biosci (Schol Ed) 01-Jan-2012
PMCID:PMC3314490
doi:10.2741/257
PMID:22202049
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
Characterization of Silvestrol Pharmacokinetics in Mice Using Liquid Chromatography–Tandem Mass Spectrometry Saradhi UV, Gupta SV, Chiu M, Wang J, Ling Y, Liu Z, Newman DJ, Covey JM, Kinghorn AD, Marcucci G, Lucas DM, Grever MR, Phelps MA, Chan KK AAPS J 16-Apr-2011
PMCID:PMC3160157
doi:10.1208/s12248-011-9273-x
PMID:21499689
Isolation and Characterization of Minor Analogues of Silvestrol and other Constituents from a Large-scale Recollection of Aglaia foveolata Pan L, Kardono LB, Riswan S, Chai H, Carcache de Blanco EJ, Pannell CM, Soejarto DD, McCloud TG, Newman DJ, Kinghorn AD J Nat Prod 12-Oct-2010
PMCID:PMC2993763
doi:10.1021/np100503q
PMID:20939540
The continuing search for antitumor agents from higher plants Pan L, Chai H, Kinghorn AD Phytochem Lett 12-Mar-2010
PMCID:PMC2836022
doi:10.1016/j.phytol.2009.11.005
PMID:20228943
The novel plant-derived agent silvestrol has B-cell selective activity in chronic lymphocytic leukemia and acute lymphoblastic leukemia in vitro and in vivo Lucas DM, Edwards RB, Lozanski G, West DA, Shin JD, Vargo MA, Davis ME, Rozewski DM, Johnson AJ, Su BN, Goettl VM, Heerema NA, Lin TS, Lehman A, Zhang X, Jarjoura D, Newman DJ, Byrd JC, Kinghorn AD, Grever MR Blood 07-May-2009
PMCID:PMC2680369
doi:10.1182/blood-2008-09-175430
PMID:19190247
Discovery of Natural Product Anticancer Agents from Biodiverse Organisms Kinghorn AD, Chin YW, Swanson SM Curr Opin Drug Discov Devel 01-Mar-2009
PMCID:PMC2877274
PMID:19333864
Discovery of anticancer agents of diverse natural origin Kinghorn AD, Carcache de Blanco EJ, Chai HB, Orjala J, Farnsworth NR, Soejarto DD, Oberlies NH, Wani MC, Kroll DJ, Pearce CJ, Swanson SM, Kramer RA, Rose WC, Fairchild CR, Vite GD, Emanuel S, Jarjoura D, Cope FO Pure Appl Chem 01-Jan-2009
PMCID:PMC2765058
doi:10.1351/PAC-CON-08-10-16
PMID:20046887
Infraspecific variation of sulfur-containing bisamides from Aglaia leptantha. Greger H, Pacher T, Vajrodaya S, Bacher M, Hofer O J Nat Prod 01-May-2000
doi:10.1021/NP990542Y
PMID:10843571

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
3-methylsulfanyl-N-[4-[(2-phenylacetyl)amino]butyl]prop-2-enamide 85152186 Click to see CSC=CC(=O)NCCCCNC(=O)CC1=CC=CC=C1 306.40 unknown https://doi.org/10.1021/NP990542Y
Aglaithioduline 10470425 Click to see CSC=CC(=O)NCCCCNC(=O)CC1=CC=CC=C1 306.40 unknown https://doi.org/10.1021/NP990542Y
> Benzenoids / Benzene and substituted derivatives / Phenylacetamides
(E)-3-methylsulfanyl-N-[(2S)-1-(2-phenylacetyl)pyrrolidin-2-yl]prop-2-enamide 163009595 Click to see CSC=CC(=O)NC1CCCN1C(=O)CC2=CC=CC=C2 304.40 unknown https://doi.org/10.1021/NP990542Y
(E)-3-methylsulfanyl-N-[1-(2-phenylacetyl)pyrrolidin-2-yl]prop-2-enamide 10733323 Click to see CSC=CC(=O)NC1CCCN1C(=O)CC2=CC=CC=C2 304.40 unknown https://doi.org/10.1021/NP990542Y
2-phenyl-N-[4-[(2-phenylacetyl)amino]butyl]acetamide 2162324 Click to see C1=CC=C(C=C1)CC(=O)NCCCCNC(=O)CC2=CC=CC=C2 324.40 unknown https://doi.org/10.1021/NP990542Y
3-methylsulfanyl-N-[1-(2-phenylacetyl)pyrrolidin-2-yl]prop-2-enamide 85249149 Click to see CSC=CC(=O)NC1CCCN1C(=O)CC2=CC=CC=C2 304.40 unknown https://doi.org/10.1021/NP990542Y
> Lignans, neolignans and related compounds / Furanoid lignans
(3aS,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 137795855 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1021/NP990542Y
Eudesmin 234823 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1021/NP990542Y
Yangambin 443028 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown https://doi.org/10.1021/NP990542Y
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(2R,3R,4R,5R)-3,4-Dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)tetrahydrofuran 10048436 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1021/NP990542Y
(2R,3S,4R,5R)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane 98683123 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1021/NP990542Y
(2S,3R,4R,5R)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)tetrahydrofuran 21603492 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1021/NP990542Y
3,4-Dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane 4485701 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1021/NP990542Y
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(5E,9E)-3,6,10-trimethyl-7,8-dihydro-4H-cyclodeca[b]furan-11-one 131881530 Click to see CC1=CCC2=C(C(=O)C(=CCC1)C)OC=C2C 230.30 unknown https://doi.org/10.1021/NP990542Y
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-1,6,10,14,18,22-hexaen-3-ol 101588274 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC(C(=C)C)O)C)C)C 426.70 unknown https://doi.org/10.1021/NP990542Y
> Organic acids and derivatives / Vinylogous thioesters
Qsbpeslwdkawrz-qpjjxvbhsa- 10750139 Click to see CSC=CC(=O)NCCCCN 188.29 unknown https://doi.org/10.1021/NP990542Y
> Organic oxygen compounds / Organooxygen compounds / Ethers / Alkyl aryl ethers
Dehydroconiferyl alcohol 129638468 Click to see COC1=C(C#CC(=C1)C=CCO)O 178.18 unknown https://doi.org/10.1021/NP990542Y
> Organoheterocyclic compounds / Pyrrolidines / N-acylpyrrolidines
(E)-3-methylsulfanyl-N-[(2R)-1-[(E)-3-methylsulfanylprop-2-enoyl]pyrrolidin-2-yl]prop-2-enamide 162874686 Click to see CSC=CC(=O)NC1CCCN1C(=O)C=CSC 286.40 unknown https://doi.org/10.1021/NP990542Y
3-methylsulfanyl-N-[1-(3-methylsulfanylprop-2-enoyl)pyrrolidin-2-yl]prop-2-enamide 85265316 Click to see CSC=CC(=O)NC1CCCN1C(=O)C=CSC 286.40 unknown https://doi.org/10.1021/NP990542Y
N-[(2R)-1-[(E)-3-methylsulfanylprop-2-enoyl]pyrrolidin-2-yl]-2-phenylacetamide 163193766 Click to see CSC=CC(=O)N1CCCC1NC(=O)CC2=CC=CC=C2 304.40 unknown https://doi.org/10.1021/NP990542Y
N-[(2S)-1-[(E)-3-methylsulfanylprop-2-enoyl]pyrrolidin-2-yl]-2-phenylacetamide 162992060 Click to see CSC=CC(=O)N1CCCC1NC(=O)CC2=CC=CC=C2 304.40 unknown https://doi.org/10.1021/NP990542Y
N-[1-(3-methylsulfanylprop-2-enoyl)pyrrolidin-2-yl]-2-phenylacetamide 85187863 Click to see CSC=CC(=O)N1CCCC1NC(=O)CC2=CC=CC=C2 304.40 unknown https://doi.org/10.1021/NP990542Y
> Organosulfur compounds / Thioethers / Thioenol ethers
N-(4-aminobutyl)-3-methylsulfanylprop-2-enamide 85255553 Click to see CSC=CC(=O)NCCCCN 188.29 unknown https://doi.org/10.1021/NP990542Y
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-Dehydrodiconiferyl alcohol 11824478 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown https://doi.org/10.1021/NP990542Y
Dehydrodiconiferyl alcohol 5372367 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown https://doi.org/10.1021/NP990542Y

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