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| Cat.No. | Product name | Product Description |
| R2032256 | Glasdegib(PF-04449913) | Glasdegib (PF-04449913) is a potent and orally bioavailable smoothened inhibitor |
| R2032257 | Gedatolisib;PKI-587;PF-05212384 | Gedatolisib (PKI-587) is a highly potent dual inhibitor of PI3Kα, PI3Kγ, and mTO |
| R2032258 | PD173074 | PD173074 is a potent FGFR1 inhibitor with an IC50 of 25 nM and also inhibits VEG |
| R2032259 | PF573228 | PF-573228 is a potent and selective FAK inhibitor with IC50 of 4 nM for purified |
| R2032260 | S1RA(E-52862) | S1RA(E-52862) is a potent and selective sigma-1 receptor(σ1R, Ki=17 nM) antagoni |
| R2032261 | RO61-8048 | Ro 61-8048 is a potent and selective inhibitor of kynurenine hydroxylase with IC |
| R2032262 | SB525334;SB-525334 | SB 525334 is a potent and selective transforming growth factor β1 receptor (ALK5 |
| R2032263 | TAK901 | TAK-901 is a multi-targeted aurora inhibitor with IC50s of 21 and 15 nM for auro |
| R2032264 | Ricolinostat;ACY-1215;Rocilinostat | Ricolinostat (ACY-1215) is a potent and selective HDAC6 inhibitor, with an IC50 |
| R2032265 | TGR5 Receptor Agonist(CCDC) | TGR5 Receptor Agonist (CCDC), a potent TGR5(GPCR19) agonist, shows improved pote |
| R2032266 | Orantinib(SU6668;TSU-68) | Orantinib (SU6668; TSU-68) is a multi-targeted receptor tyrosine kinase inhibito |
| R2032267 | WP1066 | WP1066 is an inhibitor of JAK2 and STAT3, and also shows effect on STAT5 and ERK |
| R2032268 | Mdivi-1 | Mdivi-1 is a selective dynamin-related protein 1 (Drp1) inhibitor.Mdivi-1 is a m |
| R2032269 | SAR191801;hPGDS-IN-1 | hPGDS-IN-1 is a hPGDS inhibitor ,with IC50 of 12 nM in the Fluorescence Polariza |
| R2032270 | GS967(GS-458967) | GS967 (GS-458967) is a potent, and selective inhibitor of cardiac late sodium cu |
| R2032271 | ONO-4059 analog | ONO-4059 analog is the analog of ONO-4059, ONO-4059 is a highly potent and selec |
| R2032272 | VRT-1353385;Sibofimloc(Antibiotic-202) | Sibofimloc (Antibiotic-202) is an antibiotic compound, for treating bacterial in |
| R2032273 | ADX-47273 | ADX-47273 is a positive allosteric modulator selective for the metabotropic glut |
| R2032274 | Ki16425(Debio0719) | Ki16425 (Debio 0719) is a subtype-selective, competitive antagonist of the EDG-f |
| R2032275 | SAG | SAG is a potent Smo receptor agonist which activates the Hedgehog signaling path |
| R2032276 | SB-242084 | SB 242084 is a 5-HT2C receptor antagonist(pKi=9.0) that displays 158- and 100-fo |
| R2032277 | SR9243 | SR9243 is a liver-X-receptor (LXR) inverse agonist that induces LXR-corepressor |
| R2032278 | AM-095 | AM095 (free acid) is a potent LPA1 receptor antagonist with IC50 values of 0.98 |
| R2032279 | NPS2143;NPS-2143(SB-262470A) | NPS-2143 (SB-262470A), an orally active calcilytic agent, is a selective and pot |
| R2032280 | Taselisib(GDC-0032) | Taselisib (GDC-0032) is a potent PI3K inhibitor targets PIK3CA mutations, with K |
