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在色谱分析、有机合成和交叉偶联反应领域已被 0 篇同行评审文献引用。
Crenigacestat (LY3039478) 是一种有效的Notch和 gamma-secretase 的抑制剂,其对Notch的IC50值为0.41 nM,其在多种肿瘤细胞中的 IC50 为 ∼1nM。
LY3039478具有最佳的整体特性,是独特的,显示有趣的阻转异构现象。LY3039478在血浆中的主要/次要旋转异构体的平均比例范围在14和28之间。LY3039478的结晶-水合物形式由一个单旋转异构体组成,在加速稳定性实验条件下,其化学和物理性质至少可以稳定14天。
Information
Crenigacestat (LY3039478) is an oralNotchandgamma-secretaseinhibitor with IC50 of 0.41 nM for Notch.
In vitro
LY3039478 is a novel small molecule that is an exquisitely potent inhibitor of Notch-1 intracellular domain (N1ICD) cleavage with an IC50 of ∼1nM in most of the tumor cell lines tested. LY3039478 also potently inhibits mutant Notch receptor activity. Treatment with a gamma secretase inhibitor, LY3039478, significantly inhibited the growth of 2 CCRCC(Clear cell renal cell carcinoma) cell lines in a concentration dependent manner. LY3039478 treatment also led to decreased expression of Myc and Cyclin A1, two genes that were part of the NOTCH driven proliferative signature in murine and human model systems. LY3039478 treatment also led to G0/G1 cell cycle arrest in CCRCC cells.
In vivo
In mice, its oral bioavalability(%F) is 65%, clearance(CL)=41 mL/min/kg, VDss = 3.8 L/kg. In Rats, its oral bioavalability(%F) is 65%, CL=98 mL/min/kg, VDss=4.9 L/kg. In Dogs, its oral bioavalability (%F) is 67%, CL=3.8 mL/min/kg, VDss=1.4 L/kg. In a xenograft tumor model, LY3039478 inhibited N1ICD cleavage and expression of Notch-regulated genes in the tumor microenvironment. The inhibition of Notch cleavage also resulted in the induction of apoptosis in a Notch-dependent xenograft model. In immunodeficient NSG mice xenografted with 769-P CCRCC cells, LY3039478 treatment resulted in significantly increased survival and delayed tumor growth in independent cohorts of mice demonstrating in vivo efficacy in CCRCC.
Cell Data
cell lines:
Concentrations:100 nM
Incubation Time:24, 48, 72, 96 h
Powder Purity:≥98%
| IC50 | Notch, IC50: ~1 nM |
|---|---|
| ALogP | 1.395 |
| hba_count | 4 |
| HBD Count | 3 |
| Rotatable Bond | 8 |