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Stemona aphylla

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 UUID6440225e4ef06441909300
Scientific name Stemona aphylla
Authority Craib
First published in Bull. Misc. Inform. Kew 1912: 408 (1912)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000740127
Tropicos 100262090
KEW urn:lsid:ipni.org:names:821981-1
The Plant List kew-288226
Open Tree Of Life 310608
NCBI Taxonomy 492013
IPNI 821981-1
GBIF 2863317
EOL 1082494

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
Synthesis and Biological Studies of Benzo[b]furan Derivatives: A Review from 2011 to 2022 Arce-Ramos L, Castillo JC, Becerra D Pharmaceuticals (Basel) 06-Sep-2023
PMCID:PMC10537293
doi:10.3390/ph16091265
PMID:37765074
Clinically-Relevant ABC Transporter for Anti-Cancer Drug Resistance Xiao H, Zheng Y, Ma L, Tian L, Sun Q Front Pharmacol 19-Apr-2021
PMCID:PMC8089384
doi:10.3389/fphar.2021.648407
PMID:33953682
Comparison of Anticancer Activity and HPLC-DAD Determination of Selected Isoquinoline Alkaloids from Thalictrum foetidum, Berberis sp. and Chelidonium majus Extracts Petruczynik A, Tuzimski T, Plech T, Misiurek J, Szalast K, Szymczak G Molecules 20-Sep-2019
PMCID:PMC6803846
doi:10.3390/molecules24193417
PMID:31547046
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
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
Total Synthesis of Stemaphylline N-oxide and Related C9a-Epimeric Analogs Schulte ML, Turlington ML, Phatak SS, Harp JM, Stauffer SR, Lindsley CW Chemistry 16-Aug-2013
PMCID:PMC3925759
doi:10.1002/chem.201302669
PMID:23956045
Enhancement of cellular uptake and cytotoxicity of curcumin-loaded PLGA nanoparticles by conjugation with anti-P-glycoprotein in drug resistance cancer cells Punfa W, Yodkeeree S, Pitchakarn P, Ampasavate C, Limtrakul P Acta Pharmacol Sin 14-May-2012
PMCID:PMC4010380
doi:10.1038/aps.2012.34
PMID:22580738
Secondary Metabolites from Plants Inhibiting ABC Transporters and Reversing Resistance of Cancer Cells and Microbes to Cytotoxic and Antimicrobial Agents Wink M, Ashour ML, El-Readi MZ Front Microbiol 23-Apr-2012
PMCID:PMC3332394
doi:10.3389/fmicb.2012.00130
PMID:22536197
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
Stemona alkaloids, from traditional Thai medicine, increase chemosensitivity via P-glycoprotein-mediated multidrug resistance. Chanmahasathien W, Ampasavate C, Greger H, Limtrakul P Phytomedicine 15-Jan-2011
doi:10.1016/J.PHYMED.2010.07.014
PMID:20739156
Stemofoline ethyl acetate solvate Mungkornasawakul P, Pyne SG, Ung AT, Jatisatienr A, Willis AC Acta Crystallogr Sect E Struct Rep Online 18-Jul-2009
PMCID:PMC2977317
doi:10.1107/S1600536809026889
PMID:21583572
Alkaloids from the roots of Stemona aphylla. Mungkornasawakul P, Chaiyong S, Sastraruji T, Jatisatienr A, Jatisatienr C, Pyne SG, Ung AT, Korth J, Lie W J Nat Prod 22-May-2009
doi:10.1021/NP900030Y
PMID:19374387
Alkaloids from the roots of Stemona saxorum. Wang YZ, Tang CP, Dien PH, Ye Y J Nat Prod 01-Aug-2007
doi:10.1021/NP070099O
PMID:17636953

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> 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/NP900030Y
https://doi.org/10.1021/NP100668S
(2'S)-hydroxy-(11S,12R)-dihydrostemofoline 56666694 Click to see 405.50 unknown https://doi.org/10.1021/NP100668S
(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/10.1021/NP100668S
(2S)-2-[(1S,3S,4S,5R,6S,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-yl]-3-methoxy-4-methyl-2H-furan-5-one 56666695 Click to see CCC(CC12C3CCN1C4CC2OC35C4C(C(O5)C6C(=C(C(=O)O6)C)OC)C)O 405.50 unknown https://doi.org/10.1021/NP100668S
(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 387.50 unknown https://doi.org/10.1021/NP900030Y
(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/NP070099O
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 387.50 unknown https://doi.org/10.1016/J.PHYMED.2010.07.014
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/NP900030Y
Stemofoline 44448167 Click to see 387.50 unknown https://doi.org/10.1021/NP100668S
Stemofoline 3005205 Click to see CCCCC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C 387.50 unknown https://doi.org/10.1016/J.PHYMED.2010.07.014
> Organoheterocyclic compounds / Pyrroloazepines
(2S)-2-[(2R)-2-[(9R,9aS)-2,3,5,6,7,8,9,9a-octahydro-1H-pyrrolo[1,2-a]azepin-9-yl]propyl]-4-methyl-2H-furan-5-one 162923038 Click to see 277.40 unknown https://doi.org/10.1021/NP900030Y
(3R,5S)-5-[(2R)-2-[(4R,9R,9aS)-4-oxido-2,3,5,6,7,8,9,9a-octahydro-1H-pyrrolo[1,2-a]azepin-4-ium-9-yl]propyl]-3-methyloxolan-2-one 162812217 Click to see CC1CC(OC1=O)CC(C)C2CCCC[N+]3(C2CCC3)[O-] 295.40 unknown https://doi.org/10.1021/NP900030Y
(3R,5S)-5-[(2R)-2-[(9R,9aS)-4-oxido-2,3,5,6,7,8,9,9a-octahydro-1H-pyrrolo[1,2-a]azepin-4-ium-9-yl]propyl]-3-methyloxolan-2-one 44139894 Click to see 295.40 unknown https://doi.org/10.1021/NP900030Y
2-[2-(2,3,5,6,7,8,9,9a-octahydro-1H-pyrrolo[1,2-a]azepin-9-yl)propyl]-4-methyl-2H-furan-5-one 162923037 Click to see CC1=CC(OC1=O)CC(C)C2CCCCN3C2CCC3 277.40 unknown https://doi.org/10.1021/NP900030Y
5-[2-(2,3,5,6,7,8,9,9a-octahydro-1H-pyrrolo[1,2-a]azepin-9-yl)propyl]-3-methyloxolan-2-one 56682955 Click to see 279.40 unknown https://doi.org/10.1021/NP900030Y
Stemaphylline 44139893 Click to see CC1CC(OC1=O)CC(C)C2CCCCN3C2CCC3 279.40 unknown https://doi.org/10.1021/NP070099O
https://doi.org/10.1021/NP900030Y
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(3-Hydroxy-5-methoxy-2,4-dimethylphenyl)-1-benzofuran-4-ol 641367 Click to see CC1=C(C(=C(C=C1C2=CC3=C(C=CC=C3O2)O)OC)C)O 284.31 unknown https://doi.org/10.1021/NP100668S
Stemofuran F 11130289 Click to see 298.30 unknown https://doi.org/10.1021/NP100668S
Stemofuran J 11077369 Click to see 298.30 unknown https://doi.org/10.1021/NP100668S
Stemofuran M 50994475 Click to see 300.30 unknown https://doi.org/10.1021/NP100668S
Stemofuran N 50994538 Click to see COC1=CC(=CC(=C1)C2=CC3=C(C=C(C=C3O2)OC)O)OC 300.30 unknown https://doi.org/10.1021/NP100668S
Stemofuran O 50994539 Click to see CC1=C(C(=C(C(=C1OC)C)OC)C)C2=CC3=C(C=CC=C3O2)O 312.40 unknown https://doi.org/10.1021/NP100668S
Stemofuran P 50994540 Click to see 314.30 unknown https://doi.org/10.1021/NP100668S
Stemofuran Q 50994541 Click to see 314.30 unknown https://doi.org/10.1021/NP100668S
Stemofuran R 50994542 Click to see 328.40 unknown https://doi.org/10.1021/NP100668S
> Phenylpropanoids and polyketides / Stilbenes
Stilbostemin F 636713 Click to see 288.34 unknown https://doi.org/10.1021/NP100668S

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