5-HT1A modulator 1|cas:142477-34-7|西域试剂

5-HT1A modulator 1,97.12%

产品编号：Bellancom-100290| CAS NO：142477-34-7| 分子式：C₂₁H₂₅N₃O₂S| 分子量：383.51

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货号	包装	价格	库存与货期	购买量	操作
Bellancom-100290		￥5600.00	杭州北京（现货）

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5-HT1A modulator 1

产品介绍

5-HT1A modulator 1 对 5HT_1A，肾上腺素能 α₁ 和多巴胺 D₂ 受体具有非常高的亲和力，IC₅₀ 分别为 2±0.3 nM，10±3 nM 和 40±9 nM。

生物活性

5-HT1A modulator 1 displays very high affinities for the 5HT_1A, adrenergic α₁ and dopamine D₂ receptor with IC₅₀s of 2 ±0.3 nM, 10 ± 3 nM and 40 ±9 nM, respectively.

体外研究

5-HT1A modulator 1 (Compound 24) also displays affinities for the 5HT_1B, 5-HT_2A and 5-HT_2C receptor with IC₅₀s of 300±55 nM, 500±75 nM, and 4000±440 nM, respectively.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究

5-HT1A modulator 1 (Compound 24) shows clear antagonist action at 5HT_2A receptor subtype in mice. The antagonism is nearly complete at the dose of 1 mg/kg ip for 5-HT1A modulator 1 (94% of antagonism, p<0.01). 5-HT1A modulator 1 completely blocks the stereotypies and the climbing at the dose of 1 mg/kg ip (100% of antagonism). 5-HT1A modulator 1 is also tested in rats, using the same paradigm. After oral administration, 5-HT1A modulator 1 significantly (p<0.05) reduces the hyperactivity by 50% at the doses of 2 and 4 mg/kg po, respectively 63% and 58% of antagonism for 5-HT1A modulator 1; the antagonism is complete (103% and 108%) at the respective doses of 8 and 16 mg/kg po for 5-HT1A modulator 1 (p<0.01).

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

性状

Solid

溶解性数据

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式