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395679-53-5

中文名称 395679-53-5
英文名称 SB-568849
CAS 395679-53-5
分子式 C28H31F3N2O3
分子量 500.55
MOL 文件 395679-53-5.mol
395679-53-5 结构式 395679-53-5 结构式

基本信息

中文别名
化合物 T16852
英文别名
SB-568849
[1,1'-Biphenyl]-4-carboxamide, N-[4-[2-(diethylamino)ethoxy]-3-methoxyphenyl]-N-methyl-4'-(trifluoromethyl)-

物理化学性质

储存条件-20°C储存
溶解度溶于二甲基亚砜

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302-H315-H319-H335

常见问题列表

生物活性
SB-568849 是一种黑色素浓缩激素受体 1 (MCH R1) 拮抗剂,pKi 值为 7.7。
靶点

MCH R1 receptor

体外研究

SB-568849 is a selective SLC-1 antagonist with a pK i of 7.7 as determined in radioligand binding displacement assays; coincubation of tissue with 1 μM SB-568849 for 45 min completely inhibits the MCH induced increase in corticotropin-releasing factor (CRF) release to basal levels without causing any effect on its own. The only reported MCH receptor in the rat is SLC-1, a G protein coupled receptor found throughout the brain and periphery.

体内研究

SB-568849 (Compound 15h) possesses good receptor affinity and selectivity. SB-568849 proves to be an antagonist with stability in vivo, an acceptable brain–blood ratio and oral bioavailability. SB-568849 retains affinity, demonstrates greater in vivo stability (CL b =16 mL/min/kg) and shows an acceptable brain-blood ratio of 1. SB-568849 also shows >30-fold selectivity over a wide range of monoamine receptors and is an antagonist in the FLIPR assay with a pK b of 7.7.

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