Vomilenine: Difference between revisions
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|Section1={{Chembox Identifiers |
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| CASNo = 6880-50-8 |
| CASNo = 6880-50-8 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = C9L2GUG8W2 |
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| PubChem = 11953806 |
| PubChem = 11953806 |
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| ChemSpiderID = 10128107 |
| ChemSpiderID = 10128107 |
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'''Vomilenine''' is an [[alkaloid]] that is an intermediate chemical in the biosynthesis of [[ajmaline]].<ref>{{cite journal | |
'''Vomilenine''' is an [[alkaloid]] that is an intermediate chemical in the biosynthesis of [[ajmaline]].<ref>{{cite journal |last1=von Schumann |first1=Gerald |last2=Gao |first2=Shujuan |last3=Stöckigt |first3=Joachim |date=2002 |title=Vomilenine reductase--a novel enzyme catalyzing a crucial step in the biosynthesis of the therapeutically applied antiarrhythmic alkaloid ajmaline |journal=Bioorg Med Chem |volume=10 |issue=6 |pages=1913–1918 |doi=10.1016/s0968-0896(01)00435-7 |pmid=11937349}}</ref> |
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==References== |
==References== |
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{{reflist}} |
{{reflist}} |
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[[Category: |
[[Category:Tryptamine alkaloids]] |
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[[Category:Quinolizidine alkaloids]] |
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{{alkaloid-stub}} |
{{alkaloid-stub}} |
Latest revision as of 18:01, 18 August 2022
Names | |
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IUPAC name
[(1R,10S,12R,13E,14R,16S,18R)-13-Ethylidene-14-hydroxy-8,15-diazahexacyclo[14.2.1.01,9.02,7.010,15.012,17]nonadeca-2,4,6,8-tetraen-18-yl] acetate
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Other names
21α-Hydroxy-22-norajmala-1,19-dien-17α-yl acetate
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C21H22N2O3 | |
Molar mass | 350.418 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Vomilenine is an alkaloid that is an intermediate chemical in the biosynthesis of ajmaline.[1]
References
[edit]- ^ von Schumann, Gerald; Gao, Shujuan; Stöckigt, Joachim (2002). "Vomilenine reductase--a novel enzyme catalyzing a crucial step in the biosynthesis of the therapeutically applied antiarrhythmic alkaloid ajmaline". Bioorg Med Chem. 10 (6): 1913–1918. doi:10.1016/s0968-0896(01)00435-7. PMID 11937349.