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Home > Products
| Cat.No. | Product name | Product Description |
| R11847 | New Indocyanine Green | N/A |
| R11849 | SB202190 | N/A |
| R11850 | TUBERCIDIN | N/A |
| R11852 | sutezolid | N/A |
| R11853 | AE38;AVex-73 | AVex-73 is a muscarinic M1 agonist and a moderate sigma1 receptor potentially fo |
| R11861 | 2-methyladenosine | N/A |
| R11862 | 4-Methyl-5,7-dihydroxyisobenzofuran-1(3H)-one | N/A |
| R11863 | I-BET151 (Synonyms: GSK1210151A) | I-BET151 is a BET bromodomain inhibitor which inhibits BRD4, BRD2, and BRD3 with |
| R11864 | UNC1999 | UNC1999 is a SAM-competitive, potent and selective inhibitor of EZH1/2 with IC50 |
| R11866 | ARV-825 | ARV-825 is a BRD4 degrader based on PROTAC technology. ARV-825 binds t |
| R11867 | BAY 61-3606 | BAY 61-3606 is an orally available, ATP-competitive, reversible and highly selec |
| R11868 | Takinib | Takinib is a potent and selective TAK1 inhibitor with an IC50 of 9.5 nM, which i |
| R11870 | UNC0321 | UNC0321 is a potent and selective G9a inhibitor with Ki of 63 pM, UNC0321 is the |
| R11872 | GNE-317 | GNE-317 is a PI3K/mTOR inhibitor, is able to cross the blood-brain bar |
| R11873 | Salubrinal | Salubrinal is a cell-permeable and selective inhibitor of eIF2α dephosphory |
| R11874 | YU238259 | YU238259 is an inhibitor of homology-dependent DNA repair (HDR), used for cancer |
| R11875 | Salermide | Salermide is an inhibitor of Sirt1 and Sirt2; can cause strong ca |
| R11876 | Tideglusib (Synonyms: NP031112) | Tideglusib (NP031112) is an irreversible GSK-3 inhibitor with IC50s of 5 nM and |
| R11877 | Rabusertib (Synonyms: LY2603618; IC-83) | Rabusertib (LY2603618) is a potent and selective inhibitor of Chk1 with an IC50 |
| R11878 | Aloxistatin (E64d) | Aloxistatin (E64d) is a cell-permeable and irreversible broad-spectrum cyst |
| R11879 | E-64C | N/A |
| R11880 | Saccharin 1-methylimidazole (SMI) | Saccharin 1-methylimidazole is an activator for DNA/RNA Synthesis. |
| R11881 | CeMMEC1 | CeMMEC1 is an inhibitor of BRD4, and also has high affinity for TAF1, |
| R11882 | JZL184 | JZL 184 is a potent, selective and irreversible monoacylglycerol lipas |
| R11883 | KML-29 | KML29 is a potent and selective MAGL inhibitor with IC50 = 5.9, 15, and 43 nM in |
