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Home > Products
| Cat.No. | Product name | Product Description |
| R10587 | UNC0064-12 | |
| R10590 | Kartogenin | Kartogenin is an activator of the smad4/smad5 pathway, and promotes the selectiv |
| R10591 | NSC14613; PluriSln1 | PluriSIn1 is an inhibitor of the stearoyl-coA desaturase 1 (SCD1), which is able |
| R10594 | CID2011756 | CID-2011756 is a cell-active ATP competitive and specific PKD1 inhibitor that in |
| R10597 | Tenovin-3 | Tenovin-3 is able to increase p53 levels, determined in MCF-7 cells treated for |
| R10598 | Tenovin-6 | Tenovin-6 is an inhibitor of SIRT1 and SIRT2, slightly inhibits HDAC8, and is al |
| R10599 | 3-Methyladenine; 3-MA | 3-Methyladenine (3-MA) is a selective PI3K inhibitor for Vps34 and PI3Kγ with IC |
| R10600 | Ampalex; CX-516 | Ampalex (Ampakine CX516; CX516; BDP 12) is an ampakine and nootropic that acts a |
| R10601 | CGK733 | CGK 733 is a potent and selective inhibitor of ATM/ATR with IC50 of ~200 nM. |
| R10602 | AR-A014418 | AR-A014418 is an ATP-competitive, and selective GSK3β inhibitor with IC50 and Ki |
| R10604 | Clemizole | Clemizole is a H1 histamine receptor antagonist.Recently, researchers have ident |
| R10605 | Isoindigotin | Isoindigotin is used in the therapy of Y. |
| R10607 | CAL-101;GS-1101 | CAL-101 (Idelalisib, GS-1101) is a selective p110δ inhibitor with IC50 of 2.5 nM |
| R10609 | Reversine | Reversine is a potent human A3 adenosine receptor antagonist with Ki of 0.66 μM, |
| R10610 | Dynasore | Dynasore is a cell-permeable, reversible non-competitive dynamin inhibitor of GT |
| R10611 | PD169316 | PD 169316 is a potent, cell-permeable and selective p38 MAP kinase inhibitor (IC |
| R10612 | RKI-1313 | |
| R10613 | 1246535-95-4 | |
| R10614 | HPGDS inhibitor 1 | HPGDS inhibitor 1 is a novel and selective Hematopoietic Prostaglandin D Synthas |
| R10616 | ZCL278 | ZCL278 is a selective Cdc42 GTPase inhibitor with Kd of 11.4 μM. |
| R10617 | Pracinostat (SB939) | Pracinostat (SB939) is a potent pan-HDAC inhibitor with IC50 of 40-140 nM with e |
| R10619 | AT-56 | AT-56 is am orally active inhibitor of lipocalin-type prostaglandin D synthase ( |
| R10620 | ML161 | ML-161 is an allosteric inhibitor of PAR1 with IC50 of 0.26 μM. |
| R10621 | JW55 | JW 55 is an inhibitor of the PARP domain of tankyrase 1 and 2 (TNKS1/2). |
| R10622 | Buparlisib Hydrochloride (BKM120 Hydrochloride) | NVP-BKM120 Hydrochloride is a selective PI3K inhibitor of p110 with IC50 of 52 n |
