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Stemona burkillii

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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 UUID6440269795534316654865
Scientific name Stemona burkillii
Authority Prain
First published in J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 73: 43 (1902)

Description Top

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Synonyms Top

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Common names Top

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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
    • Indian Subcontinent
      • Bangladesh
    • Indo-China
      • Myanmar
      • Thailand

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000770113
Tropicos 100262093
KEW urn:lsid:ipni.org:names:742801-1
The Plant List kew-308840
Open Tree Of Life 310616
NCBI Taxonomy 492014
IPNI 742801-1
GBIF 2863342
EOL 1089005

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
Quality evaluation with reference to clitoriacetal and in vitro antioxidant activities of Clitoria macrophylla root Pitakpawasutthi Y, Suwatronnakorn M, Issaravanich S, Palanuvej C, Ruangrungsi N J Adv Pharm Technol Res 01-Oct-2019
PMCID:PMC6844003
doi:10.4103/japtr.JAPTR_67_19
PMID:31742117
Herbal Bioenhancers in Veterinary Phytomedicine Yurdakok-Dikmen B, Turgut Y, Filazi A Front Vet Sci 10-Oct-2018
PMCID:PMC6191517
doi:10.3389/fvets.2018.00249
PMID:30364115
A Pharmacological Strategy Using Stemofoline for more Efficacious Chemotherapeutic Treatments Against Human Multidrug Resistant Leukemic Cells Umsumarng S, Mapoung S, Yodkeeree S, Pyne SG, Dejkriengkraikul PL Asian Pac J Cancer Prev 01-Jan-2018
PMCID:PMC6428543
doi:10.31557/APJCP.2018.19.12.3533
PMID:30583680
Natural Products as Alternative Choices for P-Glycoprotein (P-gp) Inhibition Dewanjee S, K. Dua T, Bhattacharjee N, Das A, Gangopadhyay M, Khanra R, Joardar S, Riaz M, De Feo V, Zia-Ul-Haq M Molecules 25-May-2017
PMCID:PMC6152721
doi:10.3390/molecules22060871
PMID:28587082
Structural relationships of stemona alkaloids: assessment of species-specific accumulation trends for exploiting their biological activities. Kongkiatpaiboon S, Schinnerl J, Felsinger S, Keeratinijakal V, Vajrodaya S, Gritsanapan W, Brecker L, Greger H J Nat Prod 23-Sep-2011
doi:10.1021/NP2004374
PMID:21902195
Biochemical Mechanism of Modulation of Human P-glycoprotein by Stemofoline Chanmahasathien W, Ohnuma S, Ambudkar SV, Limtrakul P Planta Med 22-Jul-2011
PMCID:PMC3725602
doi:10.1055/s-0031-1280054
PMID:21786221
Phytochemical investigations of Stemona curtisii and synthetic studies on stemocurtisine alkaloids. Chaiyong S, Jatisatienr A, Mungkornasawakul P, Sastraruji T, Pyne SG, Ung AT, Urathamakul T, Lie W J Nat Prod 29-Nov-2010
doi:10.1021/NP100474Y
PMID:21049906
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
Phytochemical studies on Stemona burkillii prain: two new dihydrostemofoline alkaloids. Mungkornasawakul P, Pyne SG, Jatisatienr A, Lie W, Ung AT, Issakul K, Sawatwanich A, Supyen D, Jatisatienr C J Nat Prod 01-Oct-2004
doi:10.1021/NP049791Z
PMID:15497953
Antioxidant dehydrotocopherols as a new chemical character of Stemona species. Brem B, Seger C, Pacher T, Hartl M, Hadacek F, Hofer O, Vajrodaya S, Greger H Phytochemistry 01-Oct-2004
doi:10.1016/J.PHYTOCHEM.2004.08.023
PMID:15464160

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 / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(2R)-2,5,7,8-tetramethyl-2-[(4R,8S)-4,8,12-trimethyltridecyl]chromen-6-ol 162911849 Click to see CC1=C(C2=C(C=CC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 428.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.023
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
(11E)-(2'S)-Hydroxystemofoline 56659796 Click to see CCC(CC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C)O 403.50 unknown https://doi.org/10.1021/NP049791Z
(2'S)-Hydroxystemofoline 56666693 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
(2R)-2-[(1S,3S,4S,5R,6R,8S,9S,13R)-9-butyl-4-methyl-2,14-dioxa-10-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-yl]-3-methoxy-4-methyl-2H-furan-5-one 162879269 Click to see CCCCC12C3CCN1C4CC2OC35C4C(C(O5)C6C(=C(C(=O)O6)C)OC)C 389.50 unknown https://doi.org/10.1021/NP049791Z
(2R)-2-[(1S,3S,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-yl]-3-methoxy-4-methyl-2H-furan-5-one 162879270 Click to see CCCCC12C3CCN1C4CC2OC35C4C(C(O5)C6C(=C(C(=O)O6)C)OC)C 389.50 unknown https://doi.org/10.1021/NP049791Z
(2R)-2-[(1S,3S,4S,5R,8S,9S,13R)-9-butyl-4-methyl-2,14-dioxa-10-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-yl]-3-methoxy-4-methyl-2H-furan-5-one 163186368 Click to see CCCCC12C3CCN1C4CC2OC35C4C(C(O5)C6C(=C(C(=O)O6)C)OC)C 389.50 unknown https://doi.org/10.1021/NP049791Z
(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/10.1021/NP049791Z
(5Z)-5-[(1R,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 162859382 Click to see CCCCC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C 387.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.03.002
(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/10.1021/NP049791Z
(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/10.1021/NP049791Z
2-(9-butyl-4-methyl-2,14-dioxa-10-azapentacyclo[6.5.1.01,5.06,10.09,13]tetradecan-3-yl)-3-methoxy-4-methyl-2H-furan-5-one 72962452 Click to see CCCCC12C3CCN1C4CC2OC35C4C(C(O5)C6C(=C(C(=O)O6)C)OC)C 389.50 unknown https://doi.org/10.1021/NP049791Z
5-(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 388032 Click to see CCCCC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C 387.50 unknown https://doi.org/10.1021/NP049791Z
https://doi.org/10.1021/NP2004374
https://doi.org/10.1021/NP100474Y
5-[9-(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 72996943 Click to see CCC(CC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C)O 403.50 unknown https://doi.org/10.1021/NP049791Z
https://doi.org/10.1021/NP2004374
Stemofoline 3005205 Click to see CCCCC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C 387.50 unknown https://doi.org/10.1021/NP2004374
https://doi.org/10.1021/NP049791Z
> Organoheterocyclic compounds / Pyrrolizidines
(5E)-5-[(2R)-2-[(1S,2S,6R,7R,8R,9S)-2-butyl-7-hydroxy-11-oxa-3-azatetracyclo[5.3.1.02,6.03,9]undecan-8-yl]propylidene]-4-methoxy-3-methylfuran-2-one 162910415 Click to see CCCCC12C3CCN1C4CC2OC3(C4C(C)C=C5C(=C(C(=O)O5)C)OC)O 389.50 unknown https://doi.org/10.1021/NP049791Z
(5E)-5-[(2R)-2-[(1S,2S,6R,7R,8S,9S)-2-butyl-7-hydroxy-11-oxa-3-azatetracyclo[5.3.1.02,6.03,9]undecan-8-yl]propylidene]-4-methoxy-3-methylfuran-2-one 101357726 Click to see CCCCC12C3CCN1C4CC2OC3(C4C(C)C=C5C(=C(C(=O)O5)C)OC)O 389.50 unknown https://doi.org/10.1021/NP049791Z
(5Z)-5-[(2R)-2-[(1S,2S,6R,7R,8R,9S)-2-butyl-7-hydroxy-11-oxa-3-azatetracyclo[5.3.1.02,6.03,9]undecan-8-yl]propylidene]-4-methoxy-3-methylfuran-2-one 102286592 Click to see CCCCC12C3CCN1C4CC2OC3(C4C(C)C=C5C(=C(C(=O)O5)C)OC)O 389.50 unknown https://doi.org/10.1021/NP049791Z
5-[2-(2-Butyl-7-hydroxy-11-oxa-3-azatetracyclo[5.3.1.02,6.03,9]undecan-8-yl)propylidene]-4-methoxy-3-methylfuran-2-one 72830350 Click to see CCCCC12C3CCN1C4CC2OC3(C4C(C)C=C5C(=C(C(=O)O5)C)OC)O 389.50 unknown https://doi.org/10.1021/NP049791Z

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