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| Cat.No. | Product name | Product Description |
| R240402225 | EGFR-IN-80 | EGFR-IN-80 (compound 30) is an EGFR inhibitor with a pIC50 of 10.6. |
| R240402226 | CGS8216 | CGS8216 is a benzodiazepine receptor antagonist with anxiolytic activity. |
| R240402227 | ML359 | ML359 is a potent, selctive and reversible inhibitor of protein disulfide isomer |
| R240402228 | Ampkinone | Ampkinone is an indirect AMP-activated protein kinase (AMPK) activator. |
| R240402229 | Ralfinamide(FCE-26742A) | Ralfinamide (FCE-26742A) is an orally available Na+ blocker derived from α-amino |
| R240402230 | 诺米芬辛 | Nomifensine is a norepinephrine-dopamine reuptake inhibitor, increases the amoun |
| R240402231 | BIP-135 | BIP-135 is a potent and selective ATP-competitive GSK-3 inhibitor, with IC50s of |
| R240402232 | c-Kit-IN-3 | c-Kit-IN-3 is a selective inhibitor of c-KIT kinase with IC50s of 4 nM and 8 nM |
| R240402233 | SEL120-34A monohydrochloride | SEL120-34A monohydrochloride is an ATP-competitive and selective CDK8 inhibitor, |
| R240402234 | CAY10471 | CAY10471 (TM30089) is a potent, selective, and orally active prostaglandin D2 re |
| R240402235 | 甲磺酸吉米沙星 | Gemifloxacin mesylate (SB-265805S; LB-20304a) is an orally active broad-spectrum |
| R240402236 | PPIase-Parvulin inhibitor | PPIase-Parvulin Inhibitor is a cell-permeable inhibitor of the PPIases Pin1 and |
| R240402237 | SU4312 | SU4312 is the racemate of (Z)-SU4312 and (E)-SU4312. It inhibits PDGFR and FLK-1 |
| R240402238 | 4-(4-甲基哌嗪-1-基)-7-(三氟甲基)吡咯并[1,2-a]喹喔啉 | 4-(4-Methylpiperazin-1-yl)-7-(trifluoromethyl)pyrrolo[1,2-a]quinoxaline |
| R240402240 | 甲基硫代磺酸2-[Nα-苯甲酰基苯甲酰氨基-N6-(6-生物素氨基己酰基)-L-赖氨酰胺基]乙基 | N-[(2S)-6-[6-[5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol |
| R240402241 | CJ-42794 | CJ-42794 (CJ-042794) is a potent, orally active, selective prostaglandin E recep |
| R240402242 | Amidephrine | Amidephrine is a selective agonist of alpha 1-adrenoceptor. Amidephrine inhibits |
| R240402243 | CHR-3996 | Nanatinostat (CHR-3996) is a potent, class I selective and orally active histone |
| R240402244 | H-L-Ile-Amc TFA | H-L-Ile-Amc (TFA) is an enzyme substrate, and can detect the yeasts and molds in |
| R240402245 | PD-L1-IN-1 | PD-L1-IN-1 is a potent PD-L1 inhibitor with an IC50 of 115 nM. PD-L1-IN-1 strong |
| R240402246 | PARP1-IN-5 hydrochloride | PARP1-IN-5 dihydrochloride is a low toxicity, orally active, potent and selectiv |
| R240402247 | Benzamil | Benzamil (Benzylamiloride), an Amiloride analogue, is a Na+/Ca2+ exchanger (NCX) |
| R240402248 | GAK inhibitor 49 hydrochloride | GAK inhibitor 49 hydrochloride is a potent, ATP-competitive and highly selective |
| R240402249 | TC HSD 21 | TC HSD 21 is a potent 17β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) inhibit |
| R240402250 | 3',4',5',5,7-Pentamethoxyflavanone | 3',4',5',5,7-Pentamethoxyflavanone is a natural flavonoid compound found in Neor |
