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Temanogrel

CAS No. : 887936-68-7

MCE 站：Temanogrel

产品活性：Temanogrel 是一个高选择性的 5-HT_2A 受体拮抗剂，其 K_i 值为 4.9 nM。

研究领域：GPCR/G Protein  |  Neuronal Signaling

作用靶点：5-HT Receptor

In Vitro: Temanogrel is a highly selective 5-HT_2A receptor antagonist with a K_i of 4.9 nM. Temanogrel inhibits inositol phosphate accumulation with an IC₅₀ of 5.2 nM. Temanogrel exhibits potent inhibition of serotonin mediated amplification of ADP-stimulated human and dog platelet aggregation (IC₅₀=8.7 and 23.1 nM, respectively). Pretreatment of aortic rings with Temanogrel prevents the vasoconstriction caused by 20 μM 5-HT in a concentration-dependent manner. Preincubation with Temanogrel also significantly inhibits the 5-HT-stimulated DNA synthesis with an IC₅₀ of 13±7 nM.

In Vivo: There are no differences in heart rate or mean arterial pressure between saline-treated and Temanogrel-treated groups at any time during the experiment (that is, for mean arterial pressure, P=0.508 between groups, and P=0.540 for group-time interaction). In dogs assigned to receive Temanogrel, plasma Temanogrel levels show a rapid and sustained increase, averaging 25.5±4.1, 28.7±4.6 and 31.2±4.5 ng/mL, respectively, at 10 min, 1.25 h and 2.25 h after the start of treatment.

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