5-HT3 antagonist 5 structure
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Common Name | 5-HT3 antagonist 5 | ||
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CAS Number | 901599-43-7 | Molecular Weight | 279.29 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C16H13N3O2 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of 5-HT3 antagonist 55-HT3 antagonist 5 is a quinoxalin-2-carboxamide compound, a 5-HT3 receptor antagonist. 5-HT3 antagonist 5 exerts antagonism on 5-HT3 agonist and 2-methyl-5-HT, and shows anti-depressant effect in mice[1]. |
Name | 2-Quinoxalinecarboxamide, N-(4-methoxyphenyl)- |
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Description | 5-HT3 antagonist 5 is a quinoxalin-2-carboxamide compound, a 5-HT3 receptor antagonist. 5-HT3 antagonist 5 exerts antagonism on 5-HT3 agonist and 2-methyl-5-HT, and shows anti-depressant effect in mice[1]. |
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Related Catalog | |
Target |
5-HT3 Receptor |
In Vitro | 5-HT3 antagonist 5 (compound 4c) exhibits 5-HT3 receptor antagonisms in longitudinal muscle myenteric plexus preparation from guinea pig ileum against 5-HT3 agonist, 2-methyl-5-HT, with pA2 value of 5[1]. |
In Vivo | 5-HT3 antagonist 5 (compound 4c) (1 mg/kg; i.p.; single dose) decreases the duration of immobility and shows anti-depressant effect in FST mice[1]. Animal Model: Swiss albino mice (23 ± 2 g)[1] Dosage: 1 mg/kg Administration: Intraperitoneal injection; single dose; locomotor scores tested 10 min after administration Result: Reduced the duration of immobility as compared to the vehicle-treated (control) group. Showed no effect on the locomotion of mice as observed in spontaneous locomotor activity. |
References |
Molecular Formula | C16H13N3O2 |
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Molecular Weight | 279.29 |
Storage condition | -20°C |