RECHEM
Welcome to our website!|Hot Line: 86-21-31433387|E-mail: sales@rechemscience.com
Products Category
Contact Us
| Tel: | +86-21-31433387 |
| +86-15618786686 | |
| Email: | sales@rechemscience.com |
| info@rechemscience.com | |
| QQ: | 1369748377 |
| Skype: | sales@rechemscience.com |
| Cat.No. | Product name | Product Description |
| R2032617 | GSK650394 | GSK 650394 is a novel SGK inhibitor with IC50 of 62 nM and 1 |
| R2032618 | INCB032304 | INCB032304 is a pharmaceutical intermediate. |
| R2032619 | KRCA-0008 | KRCA-0008 is a potent and selective ALK/Ack1 inhibitor with IC50 of 12 nM/4 nM f |
| R2032620 | LY2484595 | Evacetrapib is a potent and selective of CETP inhibitor, which inhibits human re |
| R2032621 | RGB-286638 | RGB-286638 is a CDK inhibitor that inhibits the kinase activity of cyclin T1-CDK |
| R2032622 | TG003 | TG003 is a potent and ATP-competitive Cdc2-like kinase (Clk) inhibitor with IC50 |
| R2032623 | Thiamet G | Thiamet G is a potent and selective inhibitor of O-GlcNAcase (OGA), which acts t |
| R2032624 | UNC0642 | UNC0642 is a potent and selective G9a/GLP inhibitor, with an IC50 of less than 2 |
| R2032625 | z-devd-fmk | Z-DEVD-FMK is a specific and irreversible caspase-3 inhibitor with IC50 of 18 μM |
| R2032626 | BMS663068;Fostemsavir(BMS-663068) | Fostemsavir (BMS-663068) is the phosphonooxymethyl prodrug of BMS-626529.Fostems |
| R2032627 | BX517(PDK1 inhibitor2) | BX517 is a potent and selective inhibitor of PDK1 with IC50 of 6 nM. |
| R2032628 | Darapladib(SB-480848) | Darapladib is a potent inhibitor of lipoprotein-associated phospholipase A2 (Lp- |
| 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 |
