Chemical Structure : RIPK2 inhibitor OD36
CAS No.: 1638644-62-8
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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---|---|---|---|
2 mg | ¥2580 | In stock | |
5 mg | ¥4980 | In stock | |
10 mg | ¥7580 | In stock | |
25 mg | Get quote | ||
100 mg | Get quote |
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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.
分子量 | 330.772 | |
分子式 | C16H15ClN4O2 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
(13Z,14E)-25-chloro-3,6-dioxa-9-aza-1(3,5)-pyrazolo[1,5-a]pyrimidina-2(1,3)-benzenacyclononaphane |
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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