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| Cat.No. | Product name | Product Description |
| R2032514 | Rigosertib(ON-01910) | Rigosertib (ON-01910) is a non-ATP-competitive inhibitor of PLK1 with IC50 of 9 |
| R2032515 | RKI-1447 | RKI-1447 is a potent small molecule inhibitor of ROCK1 and ROCK2 with IC50 value |
| R2032516 | RN486 | RN486 is a selective Btk inhibitor with an IC50 Value of 4.0 nM.IC50 Value: 4.0 |
| R2032517 | RO5126766(CH5126766) | Ro 5126766 is a first-in-class dual MEK/RAF inhibitor that allosterically inhibi |
| R2032518 | SAL003 | Sal003 is a potent, specific and cell-permeable inhibitor of the eukaryotic tran |
| R2032519 | SB1317 Hydrochloride(TG02) | SB1317 is a potent inhibitor of CDK2, JAK2, and FLT3 for the treatment of cancer |
| R2032520 | SB271046 | SB271046 Hcl is a potent, selective and orally active 5-HT6 receptor antagonist |
| R2032521 | SB505124 | SB-505124 is a selective inhibitor of TGF-β Receptor type I receptor (ALK4, ALK5 |
| R2032522 | SB743921 | SB-743921 is a potent inhibitor of the mitotic kinesin KSP (Eg5), with a Ki of 0 |
| R2032523 | SC-514 | SC-514 is a selective IKK-2 inhibitor (IC50=11.2±4.7 μM), which does not inhibit |
| R2032524 | SGC0946 | SGC0946 is a highly potent and selective DOT1L methyltransferase inhibitor with |
| R2032525 | SGX-523 | SGX-523 is a selective Met inhibitor with IC50 of 4 nM, no activity to BRAFV599E |
| R2032526 | Skepinone-L;CBS3830 | Skepinone-L (CBS3830) is a selective p38 mitogen-activated protein kinase inhibi |
| R2032527 | SKLB1002 | SKLB1002 is a potent and ATP-competitive VEGFR2 inhibitor with IC50 of 32 nM. |
| R2032528 | SKLB610 | SKLB1002 is a potent and ATP-competitive VEGFR2 inhibitor with IC50 of 32 nM. |
| R2032529 | SNS-032(BMS-387032) | SNS-032 (BMS-387032) is a selective inhibitor of CDK2, CDK7, and CDK9 with IC50s |
| R2032530 | SNS-314 Mesylate | SNS-314 is a potent and selective aurora kinase inhibitor with IC50s of 9, 31, a |
| R2032531 | SSR128129E | SSR128129E is an orally available and allosteric FGFR inhibitor with an IC50 of |
| R2032532 | SteMRegenin 1 | StemRegenin 1 is a potent aryl hydrocarbon receptor (AhR) antagonist with IC50 o |
| R2032533 | SU11274 | SU11274 is a selective Met inhibitor with IC50 of 10 nM, but has no effects on P |
| R2032534 | SU9516 | SU9516 is a potent CDK2 inhibitor, with an IC50 of 22 nM, and also shows inhibit |
| R2032535 | TAK-700(Orteronel) | TAK-700 (Orteronel) is a potent and highly selective human 17,20-lyase inhibitor |
| R2032536 | TAK733 | TAK-733 is a potent and selective MEK allosteric site inhibitor with an IC50 of |
| R2032537 | TAK875;Fasiglifam(TAK-875) | Fasiglifam (TAK-875) is a selective GPR40 agonist with EC50 of 14 nM in human GP |
| R2032538 | Talabostat Mesilate | Talabostat mesylate (Val-boroPro mesylate; PT100 mesylate) is an orally active a |
