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| Cat.No. | Product name | Product Description |
| R21122067 | Inflachromene | Inflachromene, a microglial inhibitor, binds to HMGB1 and HMGB2 and exerts anti- |
| R21122068 | KH-CB19 | KH-CB19 is a potent and highly specific inhibitor of the CDC2-like kinase isofor |
| R21122069 | SCH-51344 | SCH-51344 is an inhibitor of RAS/RAC-mediated cell morphology pathway. RAS inter |
| R21122070 | LY5 | LY5 is an inhibitor of STAT3 that acts by inhibiting cell viability, cell migrat |
| R21122071 | Centrinone | Centrinone is a selective and reversible PlK4 inhibitor with a Ki value of 0.16 |
| R21122072 | KDOAM-25 | KDOAM-25 is a potent and highly selective histone lysine demethylases 5 (KDM5) i |
| R21122073 | Stafib-1 | Stafib-1 is the first selective inhibitor of the STAT5b SH2 domain, with a Ki of |
| R21122074 | SM-21 Maleate | SM 21 is a novel sigma(2) antagonist. |
| R21122075 | NU9056 | NU9056 is a potent and selective Tip60 (KAT5) histone acetyltransferase inhibito |
| R21122076 | Jamaicin (AnCoA4) | AnCoA4 (AnCoA-4, AnCoA 4) is a potent Orai1 channel inhibitor that inhibits stor |
| R21122077 | GSK-864 | GSK864 is an isocitrate dehydrogenase 1 (IDH1) mutant inhibitor; inhibits IDH1 m |
| R21122078 | SAFit1 | SAFit1 is a FK506 binding protein 51 (FKBP51)-specific inhibitor with a Ki of 4± |
| R21122079 | LP99 | LP99, an epigenetic probe, is a potent and selective inhibitor of the BRD7 and B |
| R21122080 | RY785 | RY785 is a potent and selective voltage-gated potassium (KV2) channel inhibitor |
| R21122081 | TLR7 agonist T7 (1V209) | 1V209 (TLR7 agonist T7) is a Toll-like receptor 7 (TLR7) agonist and has anti-tu |
| R21122082 | NSC117079 | NSC117079 is a novel PHLPP inhibitor. |
| R21122083 | 2OH-BNPP1 | 2OH-BNPP1 is an inhibitor of BUB1 kinase, a Ser/Thr kinase, used for the treatme |
| R21122084 | ML381 (VU0488130) Fumarate | ML381, also known as VU0488130, is a novel M5-orthosteric antagonist possessing |
| R21122085 | CCT077791 | CCT077791 is a p300 and PCAF histone acetyltransferase activity inhibitor. |
| R21122086 | BMS-195614 | BMS 195614 is a neutral RAR α-selective antagonist (Ki = 2.5 nM) and exhibits no |
| R21122087 | A-196 | A-196 is a potent and selective inhibitor of SUV420H1 and SUV420H2 with IC50 val |
| R21122088 | DDD85646 Hydrochloride | DDD 85646 is a potent and specific double NMT1/NMT2 inhibitor with IC50 of 17 nM |
| R21122089 | UNC-4219 TFA | UNC4219 is a negative control compound for UNC3866, a potent antagonist of the m |
| R21122090 | SB674042 | SB-674042 is a potent and selective non-peptide orexin OX1 receptor antagonist ( |
| R21122091 | BRD4884 | BRD4884 is a selective inhibitor of HDAC2 that acts by enhancing the learning an |
