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| Cat.No. | Product name | Product Description |
| R2032539 | TalaMpanel(LY300164) | Talampanel (LY300164) is an orally and selective α-amino-3-hydroxy-5-methyl-4-is |
| R2032540 | TC-DAPK 6 | TC-DAPK 6 is a potent, ATP-competitive, and highly selective DAPK inhibitor (IC5 |
| R2032541 | TCS1102 | TCS 1102 is a potent, dual orexin receptor antagonist (Ki values are 0.2 and 3 n |
| R2032542 | Telotristat Etiprate(LX 1606 Hippurate) | Telotristat etiprate (LX1606 Hippurate) is a novel, orally-delivered inhibitor o |
| R2032543 | TG100-115 | TG100-115 is a selective PI3Kγ/PI3Kδ inhibitor with IC50s of 83 and 235 nM, resp |
| R2032544 | Thiazovivin | Thiazovivin is a potent ROCK inhibitor, which can protect human embryonic stem c |
| R2032545 | TiraseMtiv(CK-2017357) | Tirasemtiv is an activator of the fast skeletal muscle troponin complex. |
| R2032546 | Tivantinib(ARQ197) | Tivantinib is a novel and highly selective c-Met tyrosine kinase inhibitor with |
| R2032547 | TMC647055 | TMC647055 is a potent HCV NS5B polymerase inhibitor potentially for the treatmen |
| R2032548 | TPCA-1 | TPCA-1 is a potent and selective inhibitor of IKK-2 with IC50 of 17.9 nM.TPCA-1 |
| R2032549 | TPT-260 Dihydrochloride(NSC55712) | TPT-260 Dihydrochloride (NSC55712) is a thiophene thiourea derivative with molec |
| R2032550 | TRV-130 | Oliceridine (TRV130) is a novel mu opioid receptor (MOR) agonist that preferenti |
| R2032551 | TTNPB | TTNPB is a highly potent RAR agonist.Competitive binding assays using human RARs |
| R2032552 | Tubacin | Tubacin is a potent and selective inhibitor of HDAC6, with an IC50 value of 4 nM |
| R2032553 | TW-37 | TW-37 is a potent Bcl-2 inhibitor with Ki values of 260, 290 and 1110 nM for Mcl |
| R2032554 | UMI-77 | UMI-77 is a selective Mcl-1 inhibitor, which shows high binding affinity to Mcl- |
| R2032555 | UNC0631 | UNC 0631 is a potent G9a inhibitor with IC50 value of 4 nM.IC50 value: 4 nM Targ |
| R2032556 | UNC2250 | UNC2250 is a potent and selective Mer inhibitor with an IC50 of 1.7 nM, about 16 |
| R2032557 | UNC2881 | UNC2881 is a potent and specific Mer kinase inhibitor; inhibits steady-state Mer |
| R2032558 | VE-821 | VE-821 is a potent ATP-competitive inhibitor of ATR with Ki/IC50 of 13 nM/26 nM. |
| R2032559 | Verdinexor(KPT-335) | Verdinexor(KPT-335) is a novel, orally bioavailable selective inhibitor of nucle |
| R2032560 | VS-5584 | VS-5584 is a pan-PI3K/mTOR kinase inhibitor with IC50s of 16 nM, 68 nM, 42 nM, 2 |
| R2032561 | VX-702 | VX-702 is a highly selective inhibitor of p38α MAPK, 14-fold higher potency agai |
| R2032562 | VX745;Neflamapimod(VX-745) | Neflamapimod (VX-745) is a potent, blood-brain barrier penetrant, highly selecti |
| R2032563 | Belnacasan(VX-765) | Belnacasan (VX-765) is an orally bioactive prodrug of VRT-043198, which is a pot |
