38990-03-3
Chemical Structure
Gelsevirine
- CAS No.: 38990-03-3
- Formula:C21H24N2O3
- Molecular Weight:352.43
IUPAC Name: (3S,3'S,3a'S,5'R,8'S,8a'S,9'R)-1-methoxy-1'-methyl-3'-vinyl-2',3',3a',7',8',8a'-hexahydro-1'H,5'H-spiro[indoline-3,4'-[3,8,5](epiethane[1,1,2]triyl)oxepino[4,5-b]pyrrol]-2-one
InChIKey: SSSCMFCWHWCCEH-MTYPYGCKSA-N
SMILES: O=C1[C@]([C@H](OC2)C[C@@H]3[C@@]2([H])[C@@]4([H])N5C)(C6=CC=CC=C6N1OC)[C@]4([H])[C@]3(C5)C=C
Biological Activity: Gelsevirine is the major alkaloid in Gelsemium elegans with potent anxiolytic effects. The anxiolytic mechanism of Gelsevirine may be involved in the agonist action of the glycine receptor in the brain. Gelsevirine has anti-proliferation activity with IC50 values of 1.41 mM and 1.22 mM for SW480 cells and MGC80-3 cells, respectively[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Gelsevirine | 98.80% | Gelsevirine is the major alkaloid in Gelsemium elegans with potent anxiolytic effects. The anxiolytic mechanism of Gelsevirine may be involved in the agonist action of the glycine receptor in the brain. Gelsevirine has anti-proliferation activity with IC50 values of 1.41 mM and 1.22 mM for SW480 cells and MGC80-3 cells, respectively. | ||||||||||||||||||||
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- [1]. Hua-Hai Zhang, et al. Characterization of Gelsevirine Metabolites in Rat Liver S9 by Accurate Mass Measurements Using High-Performance Liquid chromatography/quadrupole-time-of-flight Mass Spectrometry. Rapid Commun Mass Spectrom. 2019 Jul 30;33(14):1179-1 [Content Brief]
- [2]. Ming Liu, et al. The Active Alkaloids of Gelsemium Elegans Benth. Are Potent Anxiolytics. Psychopharmacology (Berl). 2013 Feb;225(4):839-51. [Content Brief]
- [3]. HUANG Jing, et al. Cytotoxic effects of alkaloidal compounds from Gelsemium elegans Benth on the tumor cells of digestive system in vitro. Strait Pharmaceutical Journal, 2010 , 22 (3) :197-200.
Keywords
