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Stemona curtisii

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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 UUID64402697d47ca013478275
Scientific name Stemona curtisii
Authority Hook.f.
First published in Fl. Brit. India 6: 298 (1892)

Description 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
  • Asia-tropical
    • Indian Subcontinent
      • Sri Lanka
    • Indo-China
      • Nicobar Nicobar
      • Thailand
    • Malesia
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000770114
Tropicos 50321566
KEW urn:lsid:ipni.org:names:742802-1
The Plant List kew-308841
Open Tree Of Life 310604
NCBI Taxonomy 492018
IPNI 742802-1
GBIF 2863319
EOL 1089006

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
The Optimization of Medium Conditions and Auxins in the Induction of Adventitious Roots of Pokeweed (Phytolacca americana L.) and Their Phytochemical Constituents Trunjaruen A, Luecha P, Taratima W Scientifica (Cairo) 21-Aug-2023
PMCID:PMC10462441
doi:10.1155/2023/2983812
PMID:37645570
Acaricidal and repellent activities of ethanol extracts of nine chinese medicinal herbs against Rhipicephalus microplus (Acari: Ixodidae) Li D, Lu S, Jian Y, Cheng S, Zhao Q, Yuan H, Wang N, Liu Y, Zhang S, Zhang L, Wang R, Jian F Exp Appl Acarol 31-Jul-2023
PMCID:PMC10462553
doi:10.1007/s10493-023-00813-3
PMID:37522955
Integrative Alternative Tactics for Ixodid Control Showler AT, Saelao P Insects 18-Mar-2022
PMCID:PMC8948879
doi:10.3390/insects13030302
PMID:35323601
The Role of Genetic Pathways in the Development of Chemoradiation Resistance in Nasopharyngeal Carcinoma (NPC) Patients Mat Lazim N, Che Lah CI, Wan Juhari WK, Sulong S, Zilfalil BA, Abdullah B Genes (Basel) 21-Nov-2021
PMCID:PMC8619242
doi:10.3390/genes12111835
PMID:34828441
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
Thai plants with high antioxidant levels, free radical scavenging activity, anti-tyrosinase and anti-collagenase activity Chatatikun M, Chiabchalard A BMC Complement Altern Med 09-Nov-2017
PMCID:PMC5679376
doi:10.1186/s12906-017-1994-7
PMID:29121910
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
Discovering Natural Product Modulators to Overcome Multidrug Resistance in Cancer Chemotherapy Wu CP, Ohnuma S, Ambudkar SV Curr Pharm Biotechnol 01-Apr-2011
PMCID:PMC3337630
doi:10.2174/138920111795163887
PMID:21118092
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
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
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 and larvicidal studies on Stemona curtisii: structure of a new pyrido[1,2-a]azepine Stemona alkaloid. Mungkornasawakul P, Pyne SG, Jatisatienr A, Supyen D, Jatisatienr C, Lie W, Ung AT, Skelton BW, White AH J Nat Prod 01-Apr-2004
doi:10.1021/NP034066U
PMID:15104502
Stemocurtisine, the First Pyrido[1,2-<i>a</i>]azapine <i>Stemona</i> Alkaloid. Pitchaya Mungkornasawakul, Stephen G. Pyne, Araya Jatisatienr, Damrat Supyen, Wilford Lie, Alison T. Ung, Brian W. Skelton, Allan H. White American Chemical Society (ACS) 24-Oct-2003
doi:10.1021/NP030387U
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
(5E)-4-methoxy-3-methyl-5-[(1R,6S,8R,9R,10R,11S)-11-methyl-6-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-13,14-dioxa-5-azatetracyclo[6.5.1.01,10.05,9]tetradecan-12-ylidene]furan-2-one 162891913 Click to see CC1CC(OC1=O)C2CC3C4N2CCCC5(C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C)O3 431.50 unknown https://doi.org/10.1021/NP100474Y
(5E)-4-methoxy-3-methyl-5-[(1S,2R,3S,11S)-3-methyl-11-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-5-oxa-10-azatricyclo[8.3.0.02,6]tridec-6-en-4-ylidene]furan-2-one 163025247 Click to see CC1CC(OC1=O)C2CCC3N2CCC=C4C3C(C(=C5C(=C(C(=O)O5)C)OC)O4)C 415.50 unknown https://doi.org/10.1016/S0031-9422(03)00332-7
(5E)-5-[(1R,2R,3S,6R,11S,13R)-13-hydroxy-3-methyl-11-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-5-oxa-10-azatricyclo[8.3.0.02,6]tridecan-4-ylidene]-4-methoxy-3-methylfuran-2-one 162892501 Click to see CC1CC(OC1=O)C2CC(C3N2CCCC4C3C(C(=C5C(=C(C(=O)O5)C)OC)O4)C)O 433.50 unknown https://doi.org/10.1021/NP100474Y
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
4-(3,4-Dimethoxybenzyl)-3-(4-hydroxybenzyl)dihydro-2(3H)-furanone 500177 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC=C(C=C3)O)OC 342.40 unknown https://doi.org/10.1021/NP100474Y
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
[(1R,2S,3Z,7R,8E,10R,13S)-9,10,13-triacetyloxy-2,7-dihydroxy-8,12,15,15-tetramethyl-5-oxo-4-bicyclo[9.3.1]pentadeca-3,8,11-trienyl]methyl acetate 102351451 Click to see CC1=C2C(C(=C(C(CC(=O)C(=CC(C(C2(C)C)CC1OC(=O)C)O)COC(=O)C)O)C)OC(=O)C)OC(=O)C 550.60 unknown https://doi.org/10.1016/S0031-9422(03)00332-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Valparane and mulinane diterpenoids
(2R,5R,6R,9S,12S,13R)-6,9,12-trimethyl-5-propan-2-yltetracyclo[7.5.0.01,13.02,6]tetradecan-12-ol 163194329 Click to see CC(C)C1CCC2C1(CCC3(C24CC4C(CC3)(C)O)C)C 290.50 unknown https://doi.org/10.1021/NP100474Y
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]chromen-6-ol 10574579 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
(2S)-2,7,8-trimethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]chromen-6-ol 11281431 Click to see CC1=C(C=C2C=CC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.023
2,5,7,8-Tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-ol 14311401 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
Dehydro-Gamma-Tocopherol 14657170 Click to see CC1=C(C=C2C=CC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.023
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-[(2R,4aR,8aR)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid 12304103 Click to see CC12CCCC(=C)C1CC(CC2)C(=C)C(=O)O 234.33 unknown https://doi.org/10.1021/NP034066U
https://doi.org/10.1021/NP2004374
https://doi.org/10.1021/NP020612S
https://doi.org/10.1021/NP100474Y
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP100474Y
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP100474Y
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
(5E)-4-methoxy-3-methyl-5-[(1R,4S,5R,6S,8S,9S)-4-methyl-9-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-2,14-dioxa-10-azatetracyclo[6.5.1.01,5.06,10]tetradecan-3-ylidene]furan-2-one 163190707 Click to see CC1CC(OC1=O)C2C3CC4N2CCCC5(C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C)O3 431.50 unknown https://doi.org/10.1021/NP034066U
(5Z)-4-methoxy-3-methyl-5-[(1R,4S,5R,6S,8S,9S)-4-methyl-9-[(2S,4S)-4-methyl-5-oxooxolan-2-yl]-2,14-dioxa-10-azatetracyclo[6.5.1.01,5.06,10]tetradecan-3-ylidene]furan-2-one 44566737 Click to see CC1CC(OC1=O)C2C3CC4N2CCCC5(C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C)O3 431.50 unknown https://doi.org/10.1021/NP034066U
1',2'-Didehyrostemofoline 56666692 Click to see CCC=CC12C3CCN1C4CC2OC35C4C(C(=C6C(=C(C(=O)O6)C)OC)O5)C 385.50 unknown https://doi.org/10.1021/NP100474Y
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/10.1016/S0031-9422(03)00332-7
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/NP100668S
> Organoheterocyclic compounds / Furofurans
(1R,9S,10R,11R,12S,13Z)-13-(3-methoxy-4-methyl-5-oxofuran-2-ylidene)-12-methyl-14,15-dioxa-5-azatetracyclo[7.5.1.01,11.05,10]pentadecan-6-one 53323980 Click to see CC1C2C3C4CCC(=O)N3CCCC2(O4)OC1=C5C(=C(C(=O)O5)C)OC 361.40 unknown https://doi.org/10.1021/NP100474Y
(1R,9S,10R,11R,12S)-12-methyl-14,15-dioxa-5-azatetracyclo[7.5.1.01,11.05,10]pentadecan-13-one 53326628 Click to see CC1C2C3C4CCCN3CCCC2(O4)OC1=O 237.29 unknown https://doi.org/10.1021/NP100474Y
(5E)-4-methoxy-3-methyl-5-[(1R,9R,10R,11R,12S)-12-methyl-14,15-dioxa-5-azatetracyclo[7.5.1.01,11.05,10]pentadecan-13-ylidene]furan-2-one 163189875 Click to see CC1C2C3C4CCCN3CCCC2(O4)OC1=C5C(=C(C(=O)O5)C)OC 347.40 unknown https://doi.org/10.1021/NP034066U
https://doi.org/10.1021/NP2004374
https://doi.org/10.1021/NP020612S
https://doi.org/10.1021/NP100474Y
(5E)-5-[(1R,6R,9R,10R,11R,12S)-6-[(1R)-1-hydroxypropyl]-12-methyl-14,15-dioxa-5-azatetracyclo[7.5.1.01,11.05,10]pentadecan-13-ylidene]-4-methoxy-3-methylfuran-2-one 162868347 Click to see CCC(C1CCC2C3N1CCCC4(C3C(C(=C5C(=C(C(=O)O5)C)OC)O4)C)O2)O 405.50 unknown https://doi.org/10.1016/S0031-9422(03)00332-7
(5E)-5-[(1R,6S,9R,10R,11R,12S)-6-[(1S)-1-hydroxypropyl]-12-methyl-14,15-dioxa-5-azatetracyclo[7.5.1.01,11.05,10]pentadecan-13-ylidene]-4-methoxy-3-methylfuran-2-one 162868348 Click to see CCC(C1CCC2C3N1CCCC4(C3C(C(=C5C(=C(C(=O)O5)C)OC)O4)C)O2)O 405.50 unknown https://doi.org/10.1021/NP034066U
https://doi.org/10.1021/NP2004374
https://doi.org/10.1021/NP100474Y
(5Z)-4-methoxy-3-methyl-5-[(1R,9R,11R,12S)-12-methyl-14,15-dioxa-5-azatetracyclo[7.5.1.01,11.05,10]pentadecan-13-ylidene]furan-2-one 163189876 Click to see CC1C2C3C4CCCN3CCCC2(O4)OC1=C5C(=C(C(=O)O5)C)OC 347.40 unknown https://doi.org/10.1021/NP020612S
(5Z)-4-methoxy-3-methyl-5-[(1R,9S,10R,11R,12S)-12-methyl-14,15-dioxa-5-azatetracyclo[7.5.1.01,11.05,10]pentadecan-13-ylidene]furan-2-one 11035419 Click to see CC1C2C3C4CCCN3CCCC2(O4)OC1=C5C(=C(C(=O)O5)C)OC 347.40 unknown https://doi.org/10.1021/NP034066U
(5Z)-5-[(1R,6S,9S,10R,11R,12S)-6-[(1S)-1-hydroxypropyl]-12-methyl-14,15-dioxa-5-azatetracyclo[7.5.1.01,11.05,10]pentadecan-13-ylidene]-4-methoxy-3-methylfuran-2-one 44566734 Click to see CCC(C1CCC2C3N1CCCC4(C3C(C(=C5C(=C(C(=O)O5)C)OC)O4)C)O2)O 405.50 unknown https://doi.org/10.1021/NP034066U
(5Z)-5-[(1S,6R,9R,10R,11R,12S)-6-[(1R)-1-hydroxypropyl]-12-methyl-14,15-dioxa-5-azatetracyclo[7.5.1.01,11.05,10]pentadecan-13-ylidene]-3-methoxy-4-methylfuran-2-one 101259884 Click to see CCC(C1CCC2C3N1CCCC4(C3C(C(=C5C(=C(C(=O)O5)OC)C)O4)C)O2)O 405.50 unknown https://doi.org/10.1016/S0031-9422(03)00332-7
4-Methoxy-3-methyl-5-(12-methyl-14,15-dioxa-5-azatetracyclo[7.5.1.01,11.05,10]pentadecan-13-ylidene)furan-2-one 85374929 Click to see CC1C2C3C4CCCN3CCCC2(O4)OC1=C5C(=C(C(=O)O5)C)OC 347.40 unknown https://doi.org/10.1021/NP100474Y
https://doi.org/10.1021/NP2004374
5-[(1R,6S,9R,10R,11R,12S)-6-[(1S)-1-hydroxypropyl]-12-methyl-14,15-dioxa-5-azatetracyclo[7.5.1.01,11.05,10]pentadecan-13-ylidene]-4-methoxy-3-methylfuran-2-one 162868344 Click to see CCC(C1CCC2C3N1CCCC4(C3C(C(=C5C(=C(C(=O)O5)C)OC)O4)C)O2)O 405.50 unknown https://doi.org/10.1021/NP100474Y
https://doi.org/10.1021/NP2004374
https://doi.org/10.1021/NP034066U
5-[6-(1-Hydroxypropyl)-12-methyl-14,15-dioxa-5-azatetracyclo[7.5.1.01,11.05,10]pentadecan-13-ylidene]-4-methoxy-3-methylfuran-2-one 72812133 Click to see CCC(C1CCC2C3N1CCCC4(C3C(C(=C5C(=C(C(=O)O5)C)OC)O4)C)O2)O 405.50 unknown https://doi.org/10.1021/NP100474Y
Stemocurtisine 11131804 Click to see CC1C2C3C4CCCN3CCCC2(O4)OC1=C5C(=C(C(=O)O5)C)OC 347.40 unknown https://doi.org/10.1021/NP020612S
https://doi.org/10.1021/NP030387U
Stemocurtisine N-Oxide 53323085 Click to see CC1C2C3C4CCC[N+]3(CCCC2(O4)OC1=C5C(=C(C(=O)O5)C)OC)[O-] 363.40 unknown https://doi.org/10.1021/NP100474Y
Stemocurtisinol 11350254 Click to see CCC(C1CCC2C3N1CCCC4(C3C(C(=C5C(=C(C(=O)O5)C)OC)O4)C)O2)O 405.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.03.002
Stemocurtisinol N-Oxide 53320016 Click to see CCC(C1CCC2C3[N+]1(CCCC4(C3C(C(=C5C(=C(C(=O)O5)C)OC)O4)C)O2)[O-])O 421.50 unknown https://doi.org/10.1021/NP100474Y
> 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/NP100474Y
Stemofuran F 11130289 Click to see CC1=C(C(=C(C(=C1O)C)OC)C)C2=CC3=C(C=CC=C3O2)O 298.30 unknown https://doi.org/10.1021/NP100474Y
Stemofuran J 11077369 Click to see CC1=C(C(=C(C=C1C2=CC3=C(C=CC=C3O2)O)OC)C)OC 298.30 unknown https://doi.org/10.1021/NP100474Y
Stemofuran K 10891313 Click to see CC1=C(C(=C(C(=C1O)C)OC)C)C2=CC3=CC=CC=C3O2 282.30 unknown https://doi.org/10.1021/NP100474Y
Stemofuran L 50900045 Click to see CC1=C(C(=C(C=C1C2=CC3=CC=CC=C3O2)OC)C)O 268.31 unknown https://doi.org/10.1021/NP100474Y

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