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Internal ID UUID644018b6b7b0d119269492
Scientific name Dysoxylum lenticellare
Authority Gillespie
First published in Bull. Bernice P. Bishop Mus. 83: 13 (1931)

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Synonyms Top

Scientific name Authority First published in
Didymocheton lenticellare (Gillespie) Harms Nat. Pflanzenfam. ed. 2 , 19b:157 (1940)

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Distribution (via POWO/KEW) Top

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Database ID/link to page
World Flora Online wfo-0000658657
Tropicos 100327685
KEW urn:lsid:ipni.org:names:578199-1
The Plant List kew-2780028
Open Tree Of Life 6124835
IPNI 578199-1
GBIF 3849659

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 CentralĀ®) and other sources (DOI number only)!
Title Authors Publication Released IDs
ChemInform Abstract: The Stem Constituents of Dysoxylum lenticellare. A. J. ALADESANMI Wiley 24-May-2016
doi:10.1002/CHIN.198844329
Additional alkaloids from the stem of Dysoxylum lenticellare Adetunji J. Aladesanmi, Joseph J. Hoffmann Elsevier BV 21-Nov-2007
doi:10.1016/S0031-9422(06)80125-1
Molluscicidal properties of the new constituents from the stem of <i>Dysoxylum lenticellare</i> on <i>Biomphalaria glabrata</i> A. J. Aladesanmi, C. O. Adewunmi Wiley 18-Oct-2006
doi:10.1002/PTR.2650040211
Molluscicidal activities of <i>Dysoxylum lenticellare</i> gillespie constituents on <i>Biomphalaria glabrata</i> say C. O. Adewunmi, A. J. Aladesanmi Wiley 18-Oct-2006
doi:10.1002/PTR.2650020211
The Constituents of Dysoxylum lenticellare. I. Phenylethylisoquinoline, Homoerythrina, and Dibenzazecine Alkaloids Adetunji J. Aladesanmi, Charles J. Kelley, John D. Leary American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50025A014
Ferrubietolide: X-ray crystal structure of a novel bis-diterpene from Dysoxylum Ienticellare Kay D. Onan, Charles J. Kelley, Chamnan Patarapanich, John D. Leary, Adetunji J. Aladesanmi Royal Society of Chemistry (RSC) 30-Mar-2004
doi:10.1039/C39850000121
A biflavonoid from Dysoxylum lenticellare gillespie Kan He, Barbara N. Timmermann, Adetunji J. Aladesanmi, Lu Zeng Elsevier BV 01-May-2003
doi:10.1016/0031-9422(96)00010-6
Molluscicidal activity of linn. and linn. Sushma Singh, D.K. Singh Elsevier BV 25-Jul-2002
doi:10.1016/S0045-6535(98)00565-7
Lenticellarine, a molluscicidal alkaloid from Dysoxylum lenticellare Adetunji J. Aladesanmi, Clement O. Adewunmi, Charles J. Kelley, John D. Leary, Ted A. Bischoff, Xiaolin Zhang, John K. Snyder Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83018-8
Phytochemical and pharmacological investigation of the cardioactive constituents of the leaf of Dysoxylum lenticellare. Aladesanmi AJ, Ilesanmi OR J Nat Prod 01-Nov-1987
doi:10.1021/NP50054A004
PMID:3443856
Isolation and Characterization of Lenticellarine, a Novel Alkaloid from Dysozylum lenticellare. Aladesanmi AJ, Kelley CJ, Leary JD Planta Med 01-Dec-1986
doi:10.1055/S-2007-969304
PMID:17345459
Two diterpenes and acetophenone from Dysoxylum lenticellare. Aladesanmi AJ, Kelley CJ, Leary JD Planta Med 01-Feb-1986
doi:10.1055/S-2007-969082
PMID:3703995

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
> Alkaloids and derivatives / Erythrina alkaloids / Homoerythrinane alkaloids
(1S,16S,17R)-4,5,6,16,17-pentamethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraene 101664515 Click to see COC1CC23C(=CC1OC)CCN2CCCC4=C(C(=C(C=C34)OC)OC)OC 389.50 unknown https://doi.org/10.1016/S0031-9422(06)80125-1
(1S,19S,20R)-9,19,20-trimethoxy-5,7-dioxa-14-azapentacyclo[12.7.0.01,17.02,10.04,8]henicosa-2,4(8),9,17-tetraene 14061842 Click to see COC1CC23C(=CC1OC)CCN2CCCC4=C(C5=C(C=C34)OCO5)OC 373.40 unknown https://doi.org/10.1002/CHIN.198844329
(1S,20S)-9,20-dimethoxy-5,7-dioxa-14-azapentacyclo[12.7.0.01,17.02,10.04,8]henicosa-2,4(8),9,17-tetraene 14061845 Click to see COC1CC=C2CCN3C2(C1)C4=CC5=C(C(=C4CCC3)OC)OCO5 343.40 unknown https://doi.org/10.1002/PTR.2650020211
3-Epi-schelhammericine 296196 Click to see COC1CC=C2CCN3C2(C1)C4=CC5=C(C=C4CCC3)OCO5 313.40 unknown https://doi.org/10.1021/NP50054A004
https://doi.org/10.1002/CHIN.198844329
https://doi.org/10.1002/PTR.2650020211
https://doi.org/10.1021/NP50025A014
4,5,6,16,17-Pentamethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraene 162967570 Click to see COC1CC23C(=CC1OC)CCN2CCCC4=C(C(=C(C=C34)OC)OC)OC 389.50 unknown https://doi.org/10.1016/S0031-9422(06)80125-1
9,19,20-Trimethoxy-5,7-dioxa-14-azapentacyclo[12.7.0.01,17.02,10.04,8]henicosa-2,4(8),9,17-tetraene 14061841 Click to see COC1CC23C(=CC1OC)CCN2CCCC4=C(C5=C(C=C34)OCO5)OC 373.40 unknown https://doi.org/10.1002/CHIN.198844329
> Alkaloids and derivatives / Phenethylisoquinoline alkaloids
Homolaudanosine 11046919 Click to see CN1CCC2=CC(=C(C=C2C1CCC3=CC(=C(C=C3)OC)OC)OC)OC 371.50 unknown https://doi.org/10.1021/NP50054A004
https://doi.org/10.1002/PTR.2650020211
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol 342803 Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCCCCC)O 424.80 unknown https://doi.org/10.1039/C39850000121
Ginnol 16057860 Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCCCCC)O 424.80 unknown https://doi.org/10.1039/C39850000121
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,4aS,4bS,8aR,10aR)-2-ethenyl-10a-methoxy-2,4b,8,8-tetramethyl-1,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene 163093814 Click to see CC1(CCCC2(C1CCC3(C2CCC(C3)(C)C=C)OC)C)C 304.50 unknown https://doi.org/10.1002/CHIN.198844329
2-Ethenyl-10a-methoxy-2,4b,8,8-tetramethyl-1,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene 14061846 Click to see CC1(CCCC2(C1CCC3(C2CCC(C3)(C)C=C)OC)C)C 304.50 unknown https://doi.org/10.1002/CHIN.198844329
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1039/C39850000121
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Isocopalane and spongiane diterpenoids
beta-Hydroxysandaracopimarene 44559814 Click to see CC1CCC2C3(CCCC(C3CCC2(C1C=C)O)(C)C)C 290.50 unknown https://doi.org/10.1021/NP50054A004
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Phyllocladene 101289537 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)C 272.50 unknown https://doi.org/10.1002/PTR.2650020211
https://doi.org/10.1002/CHIN.198844329
https://doi.org/10.1021/NP50054A004
https://doi.org/10.1039/C39850000121
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1'S,4'S,4aS,8R,9'S,10'R,11bS,12'R)-4,4,5',5',9',11b-hexamethyl-13'-propan-2-ylspiro[1,2,3,4a,5,6-hexahydronaphtho[2,1-f][1]benzofuran-8,15'-tetracyclo[10.2.2.01,10.04,9]hexadec-13-ene]-9-one 101282293 Click to see CC(C)C1=CC23CCC4C(CCCC4(C2CC1CC35C6=C(C=C7C(=C6)CCC8C7(CCCC8(C)C)C)OC5=O)C)(C)C 568.90 unknown https://doi.org/10.1039/C39850000121
https://doi.org/10.1016/S0045-6535(98)00565-7
4,4,5',5',9',11b-Hexamethyl-13'-propan-2-ylspiro[1,2,3,4a,5,6-hexahydronaphtho[2,1-f][1]benzofuran-8,15'-tetracyclo[10.2.2.01,10.04,9]hexadec-13-ene]-9-one 163002962 Click to see CC(C)C1=CC23CCC4C(CCCC4(C2CC1CC35C6=C(C=C7C(=C6)CCC8C7(CCCC8(C)C)C)OC5=O)C)(C)C 568.90 unknown https://doi.org/10.1039/C39850000121
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone 7469 Click to see CC(=O)C1=CC=C(C=C1)O 136.15 unknown https://doi.org/10.1002/PTR.2650020211
https://doi.org/10.1002/CHIN.198844329
https://doi.org/10.1021/NP50054A004
https://doi.org/10.1055/S-2007-969082
> Organoheterocyclic compounds / Azaspirodecane derivatives
methyl (1R,3S,11R,13R,14E)-3-methoxy-14-(2-methoxy-2-oxoethylidene)-9-azatetracyclo[7.5.0.01,6.011,13]tetradec-5-ene-13-carboxylate 101691088 Click to see COC1CC=C2CCN3C2(C1)C(=CC(=O)OC)C4(CC4C3)C(=O)OC 347.40 unknown https://doi.org/10.1002/PTR.2650040211
https://doi.org/10.1016/0031-9422(88)83018-8
https://doi.org/10.1055/S-2007-969304
methyl (1S,3R,4S,11S,13S,14E)-3,4-dimethoxy-14-(2-methoxy-2-oxoethylidene)-9-azatetracyclo[7.5.0.01,6.011,13]tetradec-5-ene-13-carboxylate 101664183 Click to see COC1CC23C(=CC1OC)CCN2CC4CC4(C3=CC(=O)OC)C(=O)OC 377.40 unknown https://doi.org/10.1016/S0031-9422(06)80125-1
methyl (1S,3R,4S,11S,13S,14E)-4-hydroxy-3-methoxy-14-(2-methoxy-2-oxoethylidene)-9-azatetracyclo[7.5.0.01,6.011,13]tetradec-5-ene-13-carboxylate 101664184 Click to see COC1CC23C(=CC1O)CCN2CC4CC4(C3=CC(=O)OC)C(=O)OC 363.40 unknown https://doi.org/10.1016/S0031-9422(06)80125-1
Methyl 3,4-dimethoxy-14-(2-methoxy-2-oxoethylidene)-9-azatetracyclo[7.5.0.01,6.011,13]tetradec-5-ene-13-carboxylate 163026556 Click to see COC1CC23C(=CC1OC)CCN2CC4CC4(C3=CC(=O)OC)C(=O)OC 377.40 unknown https://doi.org/10.1016/S0031-9422(06)80125-1
Methyl 4-hydroxy-3-methoxy-14-(2-methoxy-2-oxoethylidene)-9-azatetracyclo[7.5.0.01,6.011,13]tetradec-5-ene-13-carboxylate 162869799 Click to see COC1CC23C(=CC1O)CCN2CC4CC4(C3=CC(=O)OC)C(=O)OC 363.40 unknown https://doi.org/10.1016/S0031-9422(06)80125-1
> Organoheterocyclic compounds / Dibenzazecins
Dysazecine 158826 Click to see CN1CCCC2=CC3=C(C=C2C4=CC(=C(C=C4CC1)OC)OC)OCO3 355.40 unknown https://doi.org/10.1002/PTR.2650020211
https://doi.org/10.1021/NP50025A014
https://doi.org/10.1021/NP50054A004
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Dysoxyline 44559821 Click to see CN1CCC2=CC(=C(C=C2C1CCC3=CC4=C(C=C3)OCO4)OC)OC 355.40 unknown https://doi.org/10.1002/PTR.2650020211
https://doi.org/10.1021/NP50025A014
https://doi.org/10.1021/NP50054A004
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
6-[5-(5,7-Dihydroxy-4-oxochromen-2-yl)-2-methoxyphenyl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 101993112 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C5C(=C4O)C(=O)C=C(O5)C6=CC=C(C=C6)O)OC 566.50 unknown https://doi.org/10.1016/0031-9422(96)00010-6
Bilobetin 5315459 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O 552.50 unknown https://doi.org/10.1016/0031-9422(96)00010-6
Isoginkgetin 5318569 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)OC 566.50 unknown https://doi.org/10.1016/0031-9422(96)00010-6

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