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| Cat.No. | Product name | Product Description |
| R2032923 | RAF709 | RAF709 is a potent, selective, and efficacious RAF inhibitor with IC50s of 0.4 n |
| R2032924 | RO6885247 | RG7800 is a SMN2 splicing modifier.RG7800 has the potential for spinal muscular |
| R2032925 | SUN11602 | SUN11602 is a novel aniline compound with basic fibroblast growth factor-like ac |
| R2032926 | UNC3866 | UNC3866 is a potent antagonist of the CBX7-H3 interaction as determined by Alpha |
| R2032927 | BMS309403 | BMS-309403 is a potent, selective and cell-permeable inhibitor of adipocyte fatt |
| R2032928 | CCT251236 | CCT251236 is an orally available pirin ligand from a heat shock transcription fa |
| R2032929 | CPI-268456 | CPI-268456 is a potential BET bromodomain inhibitor. |
| R2032930 | BRD-6125 | FPH1 (BRD-6125) is a small molecule, which promotes expansion of iPS-derived hep |
| R2032931 | Glesatinib hydrochloride | Glesatinib hydrochloride is an inhibitor of the MET and Axl receptor tyrosine ki |
| R2032932 | Ziritaxestat(GLPG1690) | Ziritaxestat (GLPG1690) is a first-in-class autotaxin (ATX) inhibitor, with an I |
| R2032933 | IRAK inhibitor 6 | IRAK inhibitor 6 is an inhibitor of interleukin-1 receptor associated kinase 4 ( |
| R2032934 | SB649868;GSK649868 | SB-649868 is a potent and selective orally active orexin (OX) 1 and OX2 receptor |
| R2032935 | Vadadustat | Vadadustat is a novel, titratable, oral hypoxia-inducible factor prolyl hydroxyl |
| R2032936 | Valbenazine | Valbenazine is a prodrug of the (+)-α isomer of Ro 1-9569 for tardive syndrome t |
| R2032937 | VH298 | VH-298 is a highly potent inhibitor of the VHL:HIF-α interaction with a Kd value |
| R2032938 | AG881 | Vorasidenib (AG-881) is an orally available, brain penetrant second-generation d |
| R2032939 | AX-024 hcl | AX-024 is an orally available, first-in-class inhibitor of the TCR-Nck interacti |
| R2032940 | AZD3839 | AZD3839 (free base) is a potent and selective BACE1 inhibitor with IC50 of 23.6 |
| R2032941 | CFI-402257 | CFI-402257 is a highly potent and selective TTK (threonine tyrosine kinase) Inhi |
| R2032942 | Cobicistat | Cobicistat is a potent and selective inhibitor of cytochrome P450 3A (CYP3A) enz |
| R2032943 | Exatecan Mesylate | Exatecan Mesylate is a DNA topoisomerase I inhibitor, with an IC50 of 2.2 μM (0. |
| R2032944 | Glecaprevir;ABT-493 | Glecaprevir is a novel HCV NS3/4A protease inhibitor, with IC50 values ranging f |
| R2032945 | GNE140 | (R)-GNE-140 is a potent lactate dehydrogenase A (LDHA) inhibitor, with IC50s of |
| R2032946 | GSK2330672;Linerixibat | Linerixibat (GSK2330672) is a highly potent, nonabsorbable and orally active api |
| R2032947 | GSK5182 | GSK5182 is a highly selective inverse agonist of estrogen-related receptor γ (ER |
