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Product Category![abs470280544-(1H-Pyrazol-4-yl)-7-((2-(trimethylsilyl)ethoxy)-methyl)-7H-pyrrolo[2,3-d]pyrimidine 5mg](http://img55.chem17.com/gxhpic_a323760663/f497e47f819808744bebc014a1fa6a7a41797666d9f1bc1e75a2bd5a5ff1580455da27ff8c369809_190_190_5.png)
4-(1H-Pyrazol-4-yl)-7-((2-(trimethylsilyl)ethoxy)-methyl)-7H-pyrrolo[2,3-d]pyrimidine 941685-27-4
TP-808 852821-06-8 Store at -20℃ for one year（Powder）
ZM 39923 hydrochloride 1021868-92-7 ZM 39923 hydrochloride is an JAK1/3 inhibitor with pIC50 of 4.4/7.1, almost no activity to JAK2 and modestly potent to EGFR
CID755673 521937-07-5 CID755673 is a potent and selective cell-active small molecule inhibitor for PKD with an IC50 of 182 nM
C646 328968-36-1 C646 is an inhibitor for histone acetyltransferase, and inhibits p300 with a Ki of 400 nM in a cell-free assay. Preferentially selective for p300 versus other acetyltransferases.
CH 223191 301326-22-7 CH 223191 is a potent and specific aryl hydrocarbon receptor (AhR) antagonist with IC50 of 30 nM.
PD184352 (CI-1040) 212631-79-3 PD184352 (CI-1040) is an ATP non-competitive MEK1/2 inhibitor with IC50 of 17 nM in cell-based assays, 100-fold more selective for MEK1/2 than MEK5. Phase 2.
IC261 186611-52-9 IC261 is a novel inhibitor of CK1, triggers the mitotic checkpoint control. The IC50 of IC261 for CK1 was 16 μM and for Cdk5 is 4.5 mM.
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