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| Cat.No. | Product name | Product Description |
| R21122042 | LEI110 | LEI110 (LEI-110) is a potent phospholipase A2 XVI (PLA2G16) inhibitor with Ki of |
| R21122043 | MYLS22 | MYLS22 is a pioneering, selective optic atrophy 1 (OPA1) inhibitor. MYLS22 can |
| R21122044 | APX001 | APX001 (APX 001A; E1210 (16 strains of Staphylococcus aureus) was a novel broad |
| R21122045 | DoPAT | |
| R21122046 | (S)FTY720 Phosphate | FTY720 (S)-Phosphate is an agonist of S1P receptor 1 (S1PR1), used in the resear |
| R21122047 | CYM50769 (ML250) | neuropeptide W/B receptor 1 (NPBWR1, GPR7) antagonist |
| R21122048 | CAY10526 | CAY10526 is a selective mPGES-1 inhibitor that acts as an inhibitor of the NF-κB |
| R21122049 | NSC-13755 | |
| R21122050 | ML261 | |
| R21122051 | Galloflavin | Galloflavin inhibits both the A and B isoforms of lactate dehydrogenase with Ki |
| R21122052 | RO2959 Hydrochloride | |
| R21122053 | HA-155(Z) | Ha-155 is a highly potent and selective ATX inhibitor with an IC50 value of 5.7 |
| R21122054 | GSK205 | GSK205 is a potent, selective TRPV4 antagonist with an IC50 of 4.19 μM for inhi |
| R21122055 | SOMG-833 | A potent, selective ATP-competitive C-Met inhibitor with an IC50 of 0.93 nM; Sh |
| R21122056 | GF-61 | |
| R21122057 | LDN-211904 Oxalate | LDN-211904 is an inhibitor of erythropoietin-producing hepatocellular carcinoma |
| R21122058 | ML00253764 hydrochloride | ML00253764 is a non-peptide, brain penetrant melanocortin MC4 receptor (MC4R) an |
| R21122059 | NBI-35965 Mesylate | NBI-35965 Mesylate is a potent and selective corticotropin-releasing factor rece |
| R21122060 | PAOPA | dopamine D2 receptor modulator. |
| R21122061 | ML-211 | ML-211 is a carbamate-based dual inhibitor of LYPLA1 (IC50 = 17 nM) and the rela |
| R21122062 | NSC-658497 | NSC-658497 is an effective inhibitor of Ras-GEF, SOS1. NSC-658497 binds to SOS1, |
| R21122063 | CX-5011 | |
| R21122064 | P11;PAFAH1b2 | PAFAH1b2 is a selective platelet-activating factor acetylhydrolases 1b2 and 1b3 |
| R21122065 | FzM1 | Frizzled4 (Fzd4) receptor and Wnt/β -catenin pathway inhibitor with pEC50 value |
| R21122066 | TMP778 | TMP778 is a potent, selective reverse agonist of RORγ T, with a FRET IC50 value |
