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Home > Products
| Cat.No. | Product name | Product Description |
| R10030 | MLN4924 | MLN4924 is a potent and selective small molecule NEDD8-activating enzyme (NAE) i |
| R10031 | BIIB-024; MLN2480 | MLN2480(BIIB-024) is an oral, selective pan-Raf kinase inhibitor in chinical tri |
| R10032 | SLx-2119 (KD-025) | SLx-2119(KD-025) is a small molecule and selective inhibitor of ROCK2 with IC50 |
| R10033 | MLN8237 | Alisertib (MLN8237) is a selective Aurora A inhibitor with IC50 of 1.2 nM in a c |
| R10034 | MK8745 | MK-8745 is a potent and selective Aurora A inhibitor with IC50 of 0.6 nM, more t |
| R10035 | MDL28170 | MDL 28170 is a cell permeable selective inhibitor of Calpain 1, a Ca2+-dependent |
| R10036 | XL880; Foretinib; GSK136308 | Foretinib (GSK1363089) is an ATP-competitive inhibitor of HGFR and VEGFR, mostly |
| R10037 | ANA12 | ANA-12 is a selective TrkB antagonist with Kd of 10 nM and 12 μM for the high an |
| R10038 | CX-4945 | CX-4945 (Silmitasertib) is a potent and selective inhibitor of CK2 (casein kinas |
| R10040 | IP-145; Duvelisib; INK1197 | Duvelisib (IPI-145, INK1197) is a novel and selective PI3K δ/γ inhibitor with Ki |
| R10041 | Vesnarinone (OPC-8212) | Vesnarinone is a quinolinone derivative, and its pharmacodynamic effects include |
| R10042 | CO1686; Rociletinib | Rociletinib (CO-1686, AVL-301) is an irreversible, mutant-selective EGFR inhibit |
| R10044 | WZ4003 | WZ4003 is a highly specific NUAK kinase inhibitor with IC50 of 20 nM and 100 nM |
| R10045 | Fluoroclebopride | |
| R10046 | TORIN1 | Torin 1 is a potent inhibitor of mTORC1/2 with IC50 of 2 nM/10 nM in cell-free a |
| R10047 | Vortioxetine | Vortioxetine (Lu AA21004) is a multimodal serotonergic agent, inhibits 5-HT1A, 5 |
| R10048 | Temsavir; BMS-626529 | BMS-626529 is a novel small-molecule attachment inhibitor that targets HIV-1 gp1 |
| R10049 | TP-808;TP808 | TP808 is an intermediate that influences the synthesis of diverse tetracycline a |
| R10054 | TAE684 | TAE684 (NVP-TAE684) is a potent and selective ALK inhibitor with IC50 of 3 nM in |
| R10056 | Tubastatin-A | Tubastatin A is a potent and selective HDAC6 inhibitor withIC50 o |
| R10058 | Masitinib | Masitinib is a novel inhibitor for Kit and PDGFRα/β with IC50 of 200 nM and 540 |
| R10060 | Nadifloxacin; Acuatim; Nadixa; OPC7251 | Nadifloxacin is a topical fluoroquinolone antibiotic for the treatment of acne v |
| R10061 | Nexavar; Bay 43-9006; Sorafenib | Sorafenib Tosylate is a multikinase inhibitor of Raf-1, B-Raf and VEGFR-2 with I |
| R10062 | SAR131675 | SAR131675 is a VEGFR3 inhibitor with IC50/Ki of 23 nM/12 nM in cell-free assays, |
| R10064 | Brivanib; BMS540215 | Brivanib is an ATP-competitive inhibitor against VEGFR2 with IC50 of 25 nM, mode |
