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Stemona cochinchinensis

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440225eaecb9779377799
Scientific name Stemona cochinchinensis
Authority Gagnep.
First published in Bull. Soc. Bot. France 81: 146 (1934)

Description Top

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Synonyms Top

Scientific name Authority First published in
Stemona hutanguriana Chuakul Kew Bull. 55: 977 (2000)

Common names Top

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Language Common/alternative name
Vietnamese bách bộ nam bộ

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000740153
Tropicos 100262094
KEW urn:lsid:ipni.org:names:821984-1
The Plant List kew-288256
Open Tree Of Life 3967328
Observations.org 524383
NCBI Taxonomy 2801494
IPNI 821984-1
GBIF 2863338
EOL 1082497
Elurikkus 319805

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
Two New N-Oxide Alkaloids from Stemona cochinchinensis Lin L, Bao H, Wang A, Tang C, Dien PH, Ye Y Molecules 03-Dec-2014
PMCID:PMC6271367
doi:10.3390/molecules191220257
PMID:25479189
New Finding of an Anti-TB Compound in the Genus Marsypopetalum (Annonaceae) from a Traditional Herbal Remedy of Laos Elkington BG, Sydara K, Newsome A, Hwang CH, Lankin DC, Simmler C, Napolitano JG, Ree R, Graham JG, Gyllenhaal C, Bouamanivong S, Souliya O, Pauli GF, Franzblau SG, Soejarto DD J Ethnopharmacol 11-Dec-2013
PMCID:PMC3933013
doi:10.1016/j.jep.2013.11.057
PMID:24333958
Phytochemical studies on Stemona aphylla: isolation of a new stemofoline alkaloid and six new stemofurans. Sastraruji T, Chaiyong S, Jatisatienr A, Pyne SG, Ung AT, Lie W J Nat Prod 28-Jan-2011
doi:10.1021/NP100668S
PMID:21126060
Biological evaluation of plants of Laos used in the treatment of tuberculosis in Lao traditional medicine Elkington BG, Southavong B, Sydara K, Souliya O, Vanthanouvong M, Nettavong K, Thammachack B, Pak DH, Riley MC, Franzblau SG, Soejarto DD Pharm Biol 01-Jan-2009
PMCID:PMC3071617
doi:10.1080/13880200802398002
PMID:21479105
Pyrrolo- and pyridoazepine alkaloids as chemical markers in Stemona species. Schinnerl J, Brem B, But PP, Vajrodaya S, Hofer O, Greger H Phytochemistry 01-May-2007
doi:10.1016/J.PHYTOCHEM.2007.03.002
PMID:17449078
Cochinchistemonine, a novel skeleton alkaloid from Stemona cochinchinensis Li-Gen Lin, Chun-Ping Tang, Pham-Huu Dien, Ren-Sheng Xu, Yang Ye Elsevier BV 08-Jan-2007
doi:10.1016/J.TETLET.2007.01.013
Insecticidal pyrido[1,2-a]azepine alkaloids and related derivatives from Stemona species. Kaltenegger E, Brem B, Mereiter K, Kalchhauser H, Kählig H, Hofer O, Vajrodaya S, Greger H Phytochemistry 01-Aug-2003
doi:10.1016/S0031-9422(03)00332-7
PMID:12877922

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 / Stemona alkaloids / Stemoamide-type alkaloids
4-methyl-2-[(1S,2R,3S,6R,11S)-3-methyl-11-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-5-oxa-10-azatricyclo[8.3.0.02,6]tridecan-4-yl]-2H-furan-5-one 11058214 Click to see CC1CC(OC1=O)C2CCC3N2CCCC4C3C(C(O4)C5C=C(C(=O)O5)C)C 389.50 unknown https://doi.org/10.1016/S0031-9422(03)00332-7
Protostemonine 25256772 Click to see CC1CC(OC1=O)C2CCC3N2CCCC4C3C(C(=C5C(=C(C(=O)O5)C)OC)O4)C 417.50 unknown https://doi.org/10.1016/S0031-9422(03)00332-7
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
(5E)-5-[(1S,4S,5R,6S,8S,9S,13R)-9-butyl-4-methyl-2,14-dioxa-10-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-ylidene]-4-methoxy-3-methylfuran-2-one 162859383 Click to see CCCCC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C 387.50 unknown https://doi.org/10.1016/S0031-9422(03)00332-7
(5Z)-5-[(1S,4S,5R,6S,8S,13R)-9-[(2S)-2-hydroxybutyl]-4-methyl-2,14-dioxa-10-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-ylidene]-4-methoxy-3-methylfuran-2-one 139031609 Click to see CCC(CC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C)O 403.50 unknown https://doi.org/10.1016/S0031-9422(03)00332-7
(5Z)-5-[(1S,4S,5R,6S,8S,13R)-9-butyl-4-methyl-2,14-dioxa-10-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-ylidene]-4-methoxy-3-methylfuran-2-one 139031145 Click to see CCCCC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C 387.50 unknown https://doi.org/10.1016/S0031-9422(03)00332-7
(5Z)-5-[(1S,4S,5R,8S,9S,13R)-9-[(2S)-2-hydroxybutyl]-4-methyl-2,14-dioxa-10-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-ylidene]-4-methoxy-3-methylfuran-2-one 163193715 Click to see CCC(CC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C)O 403.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.03.002
Stemofoline 3005205 Click to see CCCCC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C 387.50 unknown https://doi.org/10.1021/NP100668S
https://doi.org/10.1016/S0031-9422(03)00332-7
> Organoheterocyclic compounds / Azepanes
(1R,2S,3R,4R,5S,6R,11S)-4,6-dihydroxy-11-[(1S)-1-hydroxypropyl]-4'-methoxy-3,3'-dimethylspiro[10-azatricyclo[8.4.0.02,6]tetradecane-5,5'-furan]-2'-one 162994550 Click to see CCC(C1CCCC2N1CCCC3(C2C(C(C34C(=C(C(=O)O4)C)OC)O)C)O)O 409.50 unknown https://doi.org/10.1016/J.TETLET.2007.01.013
4,6-Dihydroxy-11-(1-hydroxypropyl)-4'-methoxy-3,3'-dimethylspiro[10-azatricyclo[8.4.0.02,6]tetradecane-5,5'-furan]-2'-one 162994549 Click to see CCC(C1CCCC2N1CCCC3(C2C(C(C34C(=C(C(=O)O4)C)OC)O)C)O)O 409.50 unknown https://doi.org/10.1016/J.TETLET.2007.01.013

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