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Home > Products
| Cat.No. | Product name | Product Description |
| RH131609 | W146 | W146 is a selective antagonist of sphingosine-1-phosphate receptor 1 (S1PR1) wit |
| RH131699 | AZD4144 | AZD4144 is an orally active NLRP3 inhibitor. |
| RH131700 | VER-246608 | VER-246608 is a potent and ATP-competitive inhibitor of pyruvate dehydrogenase k |
| RH131701 | RMC-7977 | RMC-7977 is a highly selective inhibitor of the active (GTP-bound) forms of KRAS |
| RH131702 | Ml-60218 | ML-60218 is a broad-spectrum RNA pol III inhibitor, with IC50s of 32 and 27 μM f |
| RH131703 | Docosahexaenoic acid (DHA) | Docosahexaenoic Acid (DHA) is an omega-3 fatty acid abundantly present brain and |
| RH131704 | LY2452473 | LY2452473 is an orally bioavailable, selective androgen receptor modulator (SARM |
| RH131705 | GSK1521498 free base | GSK1521498 free base is a potent and selective μ-opioid receptor (MOR) antagonis |
| RH131706 | Fast Violet B Salt | Fast Violet B Salt |
| RH132013 | BGB-16673 | Catadegbrutinib (BTK-IN-29) (compound 14) is an inhibitor of Btk. |
| RH132014 | VX993 | Sodium Channel inhibitor 6 (compound I) is a sodium channel inhibitor that can b |
| RH132015 | SR-2890 | WEE1 DEGRADATION INHIBITORS |
| RH132016 | Acoramidis(AG10) | Acoramidis (AG10) is an orally active and selective kinetic stabilizer of WT and |
| RH132017 | PF-07328948 | PF-07328948 is an orally effective BDK (branch chain ketoacid dehydrog |
| RH132018 | LY-3299178 | LY-3299178 |
| RH132019 | PF-07265807 | PF-07265807 |
| RH132020 | E-4031 | E-4031 is a selective hERG potassium channel blocker for use in class III anti-a |
| RH132021 | 4-(Aminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole | ABD-F, a thiol-reactive fluorogenic reagent, is employed for the detection and q |
| RH132022 | IAG933(YAP-TEAD-IN-3) | IAG933 (YAP-TEAD-IN-3) is an orally available YAP/TAZ-TEAD inhibitor。 IAG933 YAP |
| RH132023 | Luteolin | Luteolin (Luteoline), a flavanoid compound, is a potent Nrf2 inhibitor. |
| RH132024 | MAC glucuronide linker-1 | MAC glucuronide linker-1 is a claevable ADC linker for antibody-agent-conjugatio |
| RH132025 | Tuspetinib (HM43239) | Tuspetinib (HM43239) is an orally active and selective FLT3 inhibitor with IC50s |
| RH132026 | PF-06679142 | PF-06679142 (Compound 10) is a potent, orally active AMPK activator with an EC50 |
| RH132027 | PRT062607(P505-15) | PRT062607(P505-15; PRT-2607; BIIB-057) is a highly specific and potent inhibitor |
| RH132028 | Dotinurad | Dotinurad ((3,5-dichloro-4-hydroxyphenyl)(1,1-dioxidobenzo[d]thiazol-3(2H)-yl)me |
