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865608-11-3

中文名称 CMPD101
英文名称 CMPD101
CAS 865608-11-3
分子式 C24H21F3N6O
分子量 466.46
MOL 文件 865608-11-3.mol
更新日期 2024/08/14 11:20:16
865608-11-3 结构式 865608-11-3 结构式

基本信息

中文别名
化合物CMPD101
英文别名
CMPD101
Takeda101
3-[[[4-Methyl-5-(4-pyridinyl)-4H-1,2,4-triazol-3-yl]methyl]amino]-N-[[2-(trifluoromethyl)phenyl]methyl]benzamide
Benzamide, 3-[[[4-methyl-5-(4-pyridinyl)-4H-1,2,4-triazol-3-yl]methyl]amino]-N-[[2-(trifluoromethyl)phenyl]methyl]-

物理化学性质

熔点>80°C (dec.)
储存条件-20°C冷冻
溶解度可溶于DMSO(少许)、甲醇(少许)
形态固体
颜色灰白色至淡黄色

图谱信息

常见问题列表

生物活性
CMPD101 是一种高效、高选择性、膜透性的 GRK2/3 小分子抑制剂,IC50 分别为 18 nM 和 5.4 nM。CMPD101 针对 GRK1、GRK5 ROCK-2 和 PKCα 的选择性较小,IC50 值分别为 3.1 μM,2.3 μM,1.4 μM 和 8.1 μM。CMPD101 可用于心衰疾病的研究。
靶点

GRK2

18 nM (IC 50 )

GRK3

5.4 nM (IC 50 )

PKCα

8.1 μM (IC 50 )

ROCK2

1.4 μM (IC 50 )

体外研究

CMPD101 (100 μM; pre-20 mins) inhibit the internalization of β2AR, remarkably decreases the isoproterenol-induced formation of clathrin-coated vesicles and the β2AR-GFP fusion protein remained on the plasma membrane in HEK-B2 cell line. CMPD101 (3-30 μM; pre-30 minutes) produced a robust phosphorylation of Ser375, which is partially inhibited by pretreatment of cells for 30 minutes with 3 μM Cmpd101 and fully blocked by pretreatment with 30 μM Cmpd101. It also inhibits phosphorylation of MOPr at Thr370, Thr376, and Thr379 residues. CMPD101 (3-30 μM; pre-30 minutes) does not affect the DAMGO-induced increase in ERK1/2 and Elk-1 phosphorylation, at 30 μM, this compound produces a small increase in basal ERK1/2 phosphorylation in HEK 293 cells expressing HA-MOPrs.

Western Blot Analysis

Cell Line: HEK 293 cells stably expressing HA-tagged rat MOPr
Concentration: 3 μM, 30 μM
Incubation Time: Pre-30 minutes
Result: Surpressed Ser375 expression completely at a high dose.

Western Blot Analysis

Cell Line: HEK 293 cells stably expressing HA-tagged rat MOPr
Concentration: 3 μM, 30 μM
Incubation Time: Pre-30 minutes
Result: Had no effect on DAMGO-induced p-ERK1/2 and p-Elk-1 expression.
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