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RIPK2 inhibitor OD36

Chemical Structure : RIPK2 inhibitor OD36

CAS No.: 1638644-62-8

RIPK2 inhibitor OD36 (OD36)

货号: PC-36066Not For Human Use, Lab Use Only.

RIPK2 inhibitor OD36 is a potent, specific, ATP-competitive inhibitor of RIPK2 with IC50 of 5.3 nM, inhibits Tyr and Ser/Thr-directed activities of RIPK2.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

RIPK2 inhibitor OD36 is a potent, specific, ATP-competitive inhibitor of RIPK2 with IC50 of 5.3 nM, inhibits Tyr and Ser/Thr-directed activities of RIPK2。
RIPK2 inhibitor OD36 inhibits both RIPK2 tyrosine autophosphorylation as well as downstream NF-κB and MAPK signaling induced by MDP, downregulates a panel of RIPK2 kinase-dependent genes。
RIPK2 inhibitor OD36 reduces cellular infiltration in an in vivo MDP-induced peritonitis model。
RIPK2 inhibitor OD36 also shows high affinity for cyclin G-associated kinase (GAK) with Ki of 3.8 nM.

物理化学性质&存储条件

分子量 330.772
分子式 C16H15ClN4O2
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(13Z,14E)-25-chloro-3,6-dioxa-9-aza-1(3,5)-pyrazolo[1,5-a]pyrimidina-2(1,3)-benzenacyclononaphane

参考文献

1. Tigno-Aranjuez JT, et al. J Biol Chem. 2014 Oct 24;289(43):29651-64.

2. Asquith CRM, et al. J Med Chem. 2019 Feb 15. doi: 10.1021/acs.jmedchem.8b01213.

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