Name | N-{3-[2-(Dimethylamino)ethoxy]-4-methoxyphenyl}-2'-methyl-4'-(5-m ethyl-1,2,4-oxadiazol-3-yl)-4-biphenylcarboxamide hydrochloride ( 1:1) |
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Description | SB-216641A (SB-216641 hydrochloride) is a selective antagonist of 5-HT1B/D receptor. SB-216641A shows high affinity and selectivity for h5-HT1B receptors over h5-HT1D receptors. SB-216641A blocks SKF-99101H from functioning in vivo[1][2]. |
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Related Catalog | |
Target |
5-HT1B Receptor 5-HT1D Receptor |
In Vivo | SB-216641A (0.6–20 mg/kg;腹腔注射;单剂量) 在豚鼠内以剂量依赖性方式阻碍 SKF-99101H 诱导的低体温[1]。 SB-216641A (559 nmol/kg;静脉注射;单剂量) 与 5-HT1B/D 受体拮抗剂 GR-127935 联用时改善了狗注射 800 nmol/kg 舒马曲坦 Sumatriptan (HY-B0121B) 后观察到的胃松弛[2]。 Animal Model: Guinea pigs[1]. Dosage: 0.6, 2.0, 6.0 and 20.0 mg/kg. Administration: Intraperitoneal injection; single dose. Result: Significantly blocked the effects of SKF-99101H. Animal Model: Dogs[2]. Dosage: 559 nmol/kg. Administration: Intravenous injection; single dose. Result: Improved the gastric relaxation. |
References |
Molecular Formula | C28H31ClN4O4 |
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Molecular Weight | 523.02300 |
Exact Mass | 522.20300 |
PSA | 89.72000 |
LogP | 6.09670 |