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| Cat.No. | Product name | Product Description |
| R11253 | PFK-015 | PFK-015 is an effective inhibitor of PFKFB3 with IC50 of 110 nM (recombinant PFK |
| R11254 | Pirinixic acid (Wy-14643) | Pirinixic acid (Wy-14643) is a potent agonist of PPARα, with EC50s of 0.63 μM, 3 |
| R11255 | Dacinostat; NVP-LAQ824 | Dacinostat is a potent HDAC inhibitor, with an IC50 of 32 nM; Dacinostat also in |
| R11257 | Lorediplon | Lorediplon is a novel non-benzodiazepine, hypnotic drug acting as a GABAA recept |
| R11259 | L67;DNA Ligase Inhibitor | L67 is a novel, competitive human DNA ligase inhibitor, inhibits DNA ligases I a |
| R11260 | NS-398 | N/A |
| R11261 | Ritalin | N/A |
| R11262 | 3PO | N/A |
| R11263 | UPF 1069 | UPF 1069 is a PARP inhibitor, with IC50s of 8 and 0.3 μM for PARP-1 and PARP-2, |
| R11264 | SCH58261 | SCH 58261 is a potent, selective and competitive antagonist of adenosine A2A rec |
| R11272 | PHCCC | PHCCC is a Group I metabotropic glutamate receptor antagonist with EC50 of 6 uM |
| R11273 | FCCP (Synonyms: Carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone) | FCCP is an uncoupler of oxidative phosphorylation in mitochondria. FCCP induces |
| R11274 | NQDI 1 | NQDI-1 inhibits apoptosis signal-regulating kinase 1 (ASK1) with a Ki of 500 nM |
| R11275 | FITM | N/A |
| R11278 | CCF642 | CCF642 is a novel PDI-inhibiting compound with antimyeloma activity. The IC50 is |
| R11279 | IMR-1 | IMR-1 is a novel class of Notch inhibitors targeting the transcriptional activat |
| R11280 | IMR-1A | N/A |
| R11282 | SB431542 | SB-431542 is a potent and selective inhibitor of ALK5/TGF-β type I Receptor with |
| R11284 | PS48 | PS48 is an activator of PDK1 with an AC50 of 8 μM. |
| R11288 | Cytochalasin H | Cytochalasin is a cell-permeable mycotoxin binding to the barbed end of actin fi |
| R11289 | Epetraborole hydrochloride;GSK2251052 hydrochloride | Epetraborole hydrochloride is a novel leucyl-tRNA synthetase (LeuRS) inhibitor, |
| R11290 | POLYQUATERNIUM-1 | N/A |
| R11291 | AZD 3965 | AZD3965 is a selective MCT1 inhibitor with a Ki of 1.6 nM, showing 6-fold select |
| R11294 | Ceralasertib (Synonyms: AZD6738) | Ceralasertib (AZD6738) is an orally active and bioavailable inhibitor of AT |
| R11298 | Belinostat (PXD101; PX105684) | Belinostat (PXD101; PX105684) is a potent HDAC inhibitor with an IC50 of 27 nM i |
