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Home > Products
| Cat.No. | Product name | Product Description |
| R2101045 | ML191 | ML-191 is a potent, selective GPR55 antagonist with 160 nM potency for GPR55 and |
| R2101046 | ML336 | ML-336 is an inhibitor of of the Venezuelan equine encephalitis virus (VEEV) str |
| R2101047 | GW280264X | GW280264X is an ADAM17 inhibitor. |
| R2101048 | TM5007 | TM5007 is a poent inhibitor plasminogen activator inhibitor-1 (PAI-1) with IC50 |
| R2101049 | CYM2503 | CYM2503 is a positive allosteric modulator (PAM) of the GAL2 receptor that poten |
| R2101050 | YM26734 | YM-26734 is a rabbit platelet sPLA2 inhibitor that has been used to ameliorate l |
| R2101051 | G244-LM | G244-LM is a potent and specific tankyrase 1/2 inhibitor that inhibits Wnt signa |
| R2101052 | VK-II-86 | VK-II-86 is a selective ryanodine receptor type 2 (RyR2) antagonist. |
| R2101053 | ML298 | ML298 (CID53393915) is a potent, specific inhibitor of Phospholipase D2 (PLD2) w |
| R2101054 | SW155246 | SW155246 is a potent and selective DNMT1 (DNA methyltransferase 1) inhibitor wit |
| R2101055 | ML-299 | ML299 (VU0463568) is a dual inhibitor of PLD1 and PLD2 with IC50 of 6 nM and 20 |
| R2101056 | VUF11418 | VUF11418 is a nonpeptidomimetic agonist of the G protein-coupled chemokine recep |
| R2101057 | CGS-15943 | CGS15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor |
| R2101058 | NSC177223 | API-1 (NSC 177223) is a potent inhibitor of Akt that induces GSK3-dependent, β-T |
| R2101059 | ML162 | ML162 is a small-molecule probe that selectively kills cells induced to express |
| R2101060 | GSK-843 | GSK-843 (GSK'843) is a potent inhibitor of receptor-interacting protein kinase 3 |
| R2101061 | Imidazenil | Imidazenil is a GABA-A modulator that blocks the sedative effects without loweri |
| R2101062 | FIT-039 | FIT-039 is a potent, selective CDK9 inhibitor with IC50 of 5.8 uM for CKD9/cycli |
| R2101063 | SR8278 | SR8278 is a competitive synthetic antagonist of nuclear heme receptor REV-ERB. S |
| R2101064 | VPC23019 | VPC 23019 is a competitive antagonist at the S1P1 and S1P3 receptors (pKi= 7.86 |
| R2101065 | HS-1793 | HS-1793 is a stable resveratrol analog that protects cardiac against mitochondri |
| R2101066 | Mycro3 | Mycro 3 is a potent and selective inhibitor of c-Myc in whole cell assays. |
| R2101067 | RBC10 | RBC10 is an inhibitor of Ral binding to RALBP1 (the effector). |
| R2101068 | PD089828 | |
| R2101069 | CRANAD-28 |
