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143797-62-0

CAS 143797-62-0
分子式 C15H14N4O.ClH
分子量 302.763
MOL 文件 143797-62-0.mol
更新日期 2024/07/21 13:45:53
143797-62-0 结构式 143797-62-0 结构式

物理化学性质

储存条件Inert atmosphere,Room Temperature
溶解度DMSO: ~26 mg/mL, soluble
形态solid
颜色pale yellow

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H335-H315-H319
危险品标志Xi
危险类别码36/37/38
安全说明26-36
WGK Germany3
1-(1-甲基-1H-吲哚-5-基)-3-(吡啶-3-基)脲盐酸盐价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30HY-1031291-(1-甲基-1H-吲哚-5-基)-3-(吡啶-3-基)脲盐酸盐
SB-200646A
143797-62-05mg700元
2024/04/30HY-1031291-(1-甲基-1H-吲哚-5-基)-3-(吡啶-3-基)脲盐酸盐
SB-200646A
143797-62-010mM * 1mLin DMSO770元
2024/04/30S08931-(1-甲基-1H-吲哚-5-基)-3-(吡啶-3-基)脲盐酸盐
SB-200646A
143797-62-05mg975.35元

常见问题列表

生物活性
SB-200646A 是第一个对 5-HT2B/2C 的选择性超过 5-HT2A 的拮抗剂,5-HT2B,5-HT2C 和 5-HT2A 的 pKi 值分别为 7.5、6.9 和 5.2。SB-200646A 具有口服活性,在体内具有电生理和抗焦虑特性。
靶点

5-HT 2B Receptor

7.5 (pKi)

5-HT 2C Receptor

6.9 (pKi)

5-HT 2A Receptor

5.2 (pKi)

体外研究

SB200646A (4 μM) abolishes the ethanol-induced increase in miniature inhibitory postsynaptic current (mIPSC) frequency and had no effect on basal mIPSC frequency.

体内研究

SB-200646A (20 mg/kg; intravenous injection; daily; for 21 days; male albino Sprague-Dawley rats) treatment significantly decreases the number of spontaneously active ventral tegmental area (VTA) dopaminergic neurons.
The i.v. administration of 4-16 mg/kg of SB-200646A significantly increases the firing rate and % events as bursts in spontaneously active VTA dopaminergic neurons and significantly increases the % events as burst in substantia nigra pars compacta (SNC) dopaminergic neurons.

Animal Model: Male albino Sprague-Dawley rats (200-225 g at the beginning of treatment and 300-350 g at the time of the experiment)
Dosage: 20 mg/kg
Administration: Intravenous injection; daily; for 21 days
Result: Significantly decreased the number of spontaneously active ventral tegmental area (VTA) dopaminergic neurons.
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