PD-1/PD-L1-IN-23

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PD-1/PD-L1-IN-23

本产品不向个人销售，仅用作科学研究，不用于任何人体实验及非科研性质的动物实验。

CAS NO:

2597056-04-5

包装与价格：

包装	价格(元)
5mg	电议
10mg	电议

产品介绍

PD-1/PD-L1-IN-23 是一种有效的、具有口服活性的 PD-1/PD-L1 抑制剂。PD-1/PD-L1-IN-23 是 L7 的酯类前药。L7 是一种苯并[c][1,2,5]恶二唑衍生物，在生物学上被评估为 PD-L1 的抑制剂。PD-1/PD-L1-IN-23 在同基因和 PD-L1 人源化小鼠的肿瘤模型中显示出显着的抗肿瘤作用。

Cas No.	2597056-04-5
分子式	C32H30BrCl2N3O6
分子量	703.41
溶解度	DMSO : 250 mg/mL (355.41 mM; Need ultrasonic)
储存条件	Store at -20°C
General tips	For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping Condition	Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request
产品描述	PD-1/PD-L1-IN-23 is a potent and orally active inhibitor of PD-1/PD-L1. PD-1/PD-L1-IN-23 is an ester prodrug of L7. L7 is a benzo[c][1,2,5]oxadiazole derivative and biologically evaluated as inhibitors of PD-L1. PD-1/PD-L1-IN-23 displays significant antitumor effects in tumor models of syngeneic and PD-L1 humanized mice[1]. [1]. Liu L, et al. Syntheses, Biological Evaluations, and Mechanistic Studies of Benzo[c][1,2,5]oxadiazole Derivatives as Potent PD-L1 Inhibitors with In Vivo Antitumor Activity. J Med Chem. 2021;64(12):8391-8409.