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| Cat.No. | Product name | Product Description |
| R11598 | CCT251921 | CCT-251921 is a potent, selective, and orally bioavailable CDK8 inhibi |
| R11599 | OTS964 hydrochloride | OTS964 hydrochloride is an orally active, high affinity and selective TOPK (T-ly |
| R11601 | Neratinib Maleate | Neratinib is an orally available, irreversible tyrosine kinase inhibitor with IC |
| R11602 | HM61713 | Olmutinib (HM61713; BI-1482694) is an orally bioavailab and irreversible third&n |
| R11604 | Edoxaban | Edoxaban(DU-176) is an oral factor Xa (FXa) inhibitor in clinical development fo |
| R11605 | MK-571 sodium salt; L-660711 (sodium salt) | MK-571 is a selective, orally active CysLT1 receptor(Cysteinyl leukotriene recep |
| R11607 | KM 11060 | KM11060 is a novel corrector of the F508del-CFTR trafficking defect. |
| R11609 | YM90709 | YM-90709 is a novel antagonist which inhibits the binding of interleukin-5 to in |
| R11610 | SC 66 | SC66 is a novel AKT inhibitor, IC50 values of approximately 0.75 μg/ml at 72 hou |
| R11612 | K 858 | K858 selectively inhibits Eg5 ATPase activity with an IC50 of 1.3 μM. |
| R11613 | JNJ 63533054 | JNJ-63533054 is a potent and selective agonist of hGPR139 with an EC50 = 16 nM. |
| R11614 | Dimethylenastron | Dimethylenastron is an Eg5 inhibitor, which arrests cells with monopolar spindle |
| R11615 | PRT4165 | PRT4165 is a potent inhibitor of PRC1 (Polycomb-repressive complex 1)-mediated H |
| R11616 | IC 261;IC261 | IC261 is a selective, ATP-competitive CK1 inhibitor, with IC50s of 1 μM, 1 μM, 1 |
| R11617 | TAS-301 | TAS-301 is an inhibitor of smooth muscle cell migration and proliferation, inhib |
| R11618 | Semaxanib (SU5416) | Semaxanib (SU5416) is a potent and selective VEGFR(Flk-1/KDR) inhibitor wit |
| R11619 | SC79 | SC79 is a brain-penetrable Akt phosphorylation activator and an inhibitor of Akt |
| R11621 | DY131(GSK 9089) | DY131(GSK 9089) is a novel selective agonist of ERRβ and ERRγ; displays minimal |
| R11622 | Endoxifen | Endoxifen is a key active metabolite of tamoxifen (TAM) with higher affinity and |
| R11623 | ITD-1 | ITD-1 is an inducer of TGFβ type II receptor degradation-1, is a potent and high |
| R11625 | RI-1 | RI-1 is a RAD51 inhibitor with IC50 ranging from 5 to 30 μM. |
| R11630 | BMS-303141 | BMS-303141 is a potent ATP-citrate lyase (ACL) inhibitor with IC50 value of 0.13 |
| R11632 | PMPA(NAALADaseinhibitor) | 2-PMPA is a potent and selective inhibitor of glutamate carboxypeptidase II (GCP |
| R11634 | MK-0941;MK-0941 mesylate | MK-0941 is a potent, orally active and allosteric glucokinase activato |
| R11635 | Bambuterol | Bambuterol is a long acting beta-adrenoceptor agonist (LABA) used in the treatme |
