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| Cat.No. | Product name | Product Description |
| R2030200 | SB225002 | SB225002, a potent, selective and non-peptide CXCR2 antagonist, inhibits 125I-IL |
| R2030202 | Cerdulatinib Hydrochloride | Cerdulatinib (PRT-062070) is an oral active, multi-targeted tyrosine kinase inhi |
| R2030203 | BMS-986142;BMS986142 | BMS-986142 is a potent and highly selective reversible inhibitor of Bruton's tyr |
| R2030210 | ABX464;ABX-464 | ABX464 is a potent anti-HIV agent. ABX464 inhibits HIV-1 replication in stimulat |
| R2030216 | Quinupristin | Semisynthetic depsipeptide type I streptogramin. An antibacterial agent. |
| R2030217 | Pristinamycin IIA | Pristinamycin IIA (RP 12536) is a macrocyclic lactone peptolide antibiotic, deri |
| R2030219 | Trifluoperazine | Trifluoperazine is an FDA-approved antipsychotic drug for schizophrenia. It is a |
| R2030223 | ASISCHEM A93504 | |
| R2030225 | cis-Pralsetinib (cis-BLU-667) | cis-Pralsetinib (cis-BLU-667) is a highly potent and selective inhibitor of rear |
| R2030226 | Suplatast tosilate | Suplatast Tosilate (IPD 1151T) is a Th2 cytokine inhibitor that attenuates IL-2, |
| R2030227 | CPD3615-A5 | |
| R2030234 | MK-0941;MK0941 | MK-0941 free base is an orally active glucokinase activator, with EC50s of 240 a |
| R2030235 | E7046 | E7046 is an orally bioavailable and specific EP4 antagonist, with IC50 of 13.5 n |
| R2030238 | SJA710-6 | |
| R2030253 | DMU2139 | DMU2139 is a potent and specific CYP1B1 inhibitor, with IC50s of 9 nM and 795 nM |
| R2030272 | F16 | F16 is a potent growth inhibitor of the neu-overexpressing cells and also select |
| R2030273 | AZ7550 | AZ7550 is an active metabolite of AZD9291 and inhibits the activity of IGF1R wit |
| R2030274 | Evodiamine | Evodiamine is an alkaloid isolated from the fruit of Evodia rutaecarpa Bentham w |
| R2030276 | GSK180736A | Evodiamine is an alkaloid isolated from the fruit of Evodia rutaecarpa Bentham w |
| R2030277 | Erismodegib (Sonidegib; LDE225; NVP-LDE225) | Erismodegib (Sonidegib) is a potent and selective Smoothened (Smo) antagonist wi |
| R2030278 | PIK-75 HCl | PIK-75 is a DNA-PK and PI3K inhibitor, which inhibits DNA-PK, p110α and p110γ wi |
| R2030279 | PND-1186 (VS-4718; SR-2516) | PND-1186 (VS-4718; SR-2516) is a potent and reversible inhibitor of FAK with an |
| R2030280 | SB742457;Intepirdine (SB-742457; GSK-742457; RVT-101) | Intepirdine (SB742457) is a highly selective 5-HT6 receptor antagonist with pKi |
| R2030281 | TGX-221 | TGX-221 is a potent, selective, and cell membrane permeable inhibitor of the PI3 |
| R2030282 | VR23 | VR23 is a small molecule that potently inhibited the activities of trypsin-like |
