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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. |