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Cat.No. Product name Product Description
R2032629 GDC-0349 GDC-0349 is a potent and selective ATP-competitive mTOR inhibitor with a Ki of 3
R2032630 GSK-J4 GSK-J4 is a potent dual inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and U
R2032631 GSK2838232
R2032632 KN-92 hydrochloride KN-92 hydrochloride is an inactive derivative of KN-93.KN-93 is a selective inhi
R2032633 KNK437 KNK437 is a HSP inhibitor, and inhibits the induction of HSP105, HSP70, and HSP4
R2032634 Cligosiban(PF-3274167) Cligosiban (PF-3274167), a high oral bioavailability and good brain-penetrant no
R2032635 SANT-1 SANT-1 is a potent Smo antagonist, inhibits Hedgehog signaling, with IC50s of 20
R2032636 SB239063 SB 239063 is a potent, selective and orally active p38 MAPK inhibitor, exhibits
R2032637 AEE788(NVP-AEE788) AEE788 is an inhibitor of the EGFR and ErbB2 with IC50 values of 2 and 6 nM, res
R2032638 DDR1-IN-1 DDR1-IN-1 is a potent and selective DDR1 receptor tyrosine kinase inhibitor with
R2032639 Decernotinib(VX-509) Decernotinib is a potent, orally active JAK3 inhibitor, with Kis of 2.5, 11, 13
R2032640 EGF816;Nazartinib Nazartinib (EGF816) is a novel, covalent mutant-selective EGFR inhibitor, with K
R2032641 GSK5959 GSK-5959 is a potent, selective and cell permeable BRPF1 bromodomain inhibitor w
R2032642 MK8245 MK-8245 is a potent, liver-targeted stearoyl-CoA desaturase (SCD) inhibitor, wit
R2032643 NS6180 NS6180 is a novel potent and selective KCa3.1 channel inhibitor(IC50= 9 nM) prev
R2032644 OF-1 OF-1 is a selective BRPF1B and BRPF2 bromodomain inhibitor with Kd values of 100
R2032645 RQ-00203078 RQ-00203078 is a highly selective, potent and orally available TRPM8 antagonist
R2032646 T-5224 T-5224 is a transcription factor c-Fos/activator protein (AP)-1 inhibitor with a
R2032647 TCS5861528 Chembridge-5861528 is a TRPA1 channel blocker that antagonizes AITC- and 4-HNE-e
R2032648 UNC0224 UNC0224 is a potent and selective G9a inhibitor with IC50 of 15 nM in the G9a Th
R2032649 VER155008 VER-155008 is an inhibitor of Hsp70, with IC50s of 0.5 μM, 2.6 μM, and 2.6 μM fo
R2032650 Vorapaxar;SCH530348 Vorapaxar (SCH 530348), an antiplatelet agent, is a selective, orally active, an
R2032651 Voreloxin(SNS-595;AG 7352) Voreloxin (SNS-595; Vosaroxin; AG 7352) is a first-in-class topoisomerase II inh
R2032652 ZM447439 ZM-447439 is an aurora kinase inhibitor with IC50s of 110 and 130 nM for aurora
R2032653 CCT244747 CCT244747 is a potent, orally bioavailable and highly selective CHK1 inhibitor,
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