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| Cat.No. | Product name | Product Description |
| 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 |
| 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, |
| R2032654 | AVN944 | AVN-944(VX-944) is a selective, noncompetitive inhibitor of the enzyme directed |
| R2032656 | AZD-5597 | AZD-5597 is potent CDK inhibitor with in vitro anti-proliferative effects agains |
| R2032657 | BET bromodomain inhibitor | BET bromodomain inhibitor is a potent BET inhibitor extracted from patent WO/201 |
| R2032658 | B-Raf inhibitor | A Tyrosine kinase inhibitor. |
| R2032659 | BRD7552 | BRD7552 is an inducer of transcription factor PDX1, which increases insulin expr |
| R2032660 | CAY10415;MSDC0160(Mitoglitazone) | MSDC 0160 (Mitoglitazone) is a mitochondrial target of thiazolidinediones (mTOT) |
| R2032661 | CEP28122 | CEP-28122 is a highly potent and selective orally active ALK inhibitor with IC50 |
| R2032662 | CEP-37440 | CEP-37440 is a novel potent and selective Dual FAK/ALK inhibitor with IC50 s of |
| R2032663 | E-64 | E-64 (Proteinase inhibitor E 64) is a potent irreversible inhibitor against gene |
| R2032664 | EPZ011989 | EPZ011989 is a potent, selective orally bioavailable EZH2 inhibitor with Ki < |
| R2032665 | Givinostat hydrochloride monohydrate(ITF2357) | Givinostat hydrochloride monohydrate (ITF-2357 hydrochloride monohydrate) is a H |
| R2032666 | HA130 | HA130 is a selective autotaxin (ATX) inhibitor with an IC50 of 28 nM. |
| R2032667 | LY3009120 | LY3009120 is a pan RAF inhibitor which inhibits BRAFV600E, BRAFWT and CRAFWT wit |
| R2032668 | MK-5108(VX-689) | MK-5108 is a highly potent and specific inhibitor of Aurora A kinase with an IC5 |
