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| Cat.No. | Product name | Product Description |
| R2032231 | Tafluprost(AFP-168) | Tafluprost(AFP-168) is an anti-glaucoma prostaglandin (PG) analog.Target:Others |
| R2032232 | Wortmannin | Wortmannin (SL-2052; KY-12420) is a potent, selective and irreversible PI3K inhi |
| R2032233 | Relugolix | Relugolix is a novel, non-peptide, orally active gonadotropin-releasing hormone |
| R2032234 | Tirapazamine | Tirapazamine is an anticancer agent that shows selective cytotoxicity for hypoxi |
| R2032235 | Elaiophylin | Elaiophylin (Azalomycin B; Gopalamicin; Efomycin E) is an autophagy inhibitor, e |
| R2032236 | Treprostinil Sodium | Treprostinil sodium is a potent DP1 and EP2 agonist with EC50 values of 0.6±0.1 |
| R2032237 | 曲前列尼尔;Treprostinil | Treprostinil (LRX-15) is a potent DP1 and EP2 agonist with EC50 values of 0.6±0. |
| R2032238 | Terlipressin | Terlipressin is a potent vasoconstrictor that acts via V1 receptors on arteriola |
| R2032239 | GIGANTOL | Gigantol is a bibenzyl compound derived from several medicinal orchids.Giganto s |
| R2032240 | Theliatinib | Theliatinib (HMPL-309) is a potent, ATP-competitive, orally active and highly se |
| R2032241 | Fumagillin(NSC9168 | Fumagillin(NSC9168) is a complex biomolecule and used as an antimicrobial agent. |
| R2032242 | Acebilustat | Acebilustat (CTX-4430) is a leukotriene A4 hydrolase inhibitor, used for an oral |
| R2032243 | Cyclosporin B | CyclosporinB |
| R2032244 | Cyclosporin C | Cyclosporin C |
| R2032245 | CHIR-99021;CT99021 | CHIR-99021 (CT99021) is a GSK-3α/β inhibitor with an IC50 of 10 and 6.7 nM, show |
| R2032246 | CP-673451;CP673451 | CP-673451 is a potent and selective inhibitor of PDGFR with IC50s of 10 and 1 nM |
| R2032247 | CTX-0294885;CTX0294885 | CTX-0294885 is a a novel bisanilino pyrimidine; exhibits inhibitory activity aga |
| R2032248 | DAPT;GSI-IX | DAPT is a γ-secretase inhibitor with IC50s of 115 and 200 nM for total Aβ and Aβ |
| R2032249 | Dinaciclib(SCH727965) | Dinaciclib is a potent inhibitor of CDK, with IC50s of 1, 1, 3, and 4 nM for CDK |
| R2032250 | Filgotinib(GLPG0634) | Filgotinib (GLPG0634) is a selective JAK1 inhibitor with IC50 of 10 nM, 28 nM, 8 |
| R2032251 | JNJ-38877605 | JNJ-38877605 is an ATP-competitive inhibitor of c-Met with IC50 of 4 nM, 600-fol |
| R2032252 | Omipalisib;GSK2126458;GSK458 | Omipalisib (GSK2126458) is a highly selective and potent inhibitor of PI3K with |
| R2032253 | GSK343 | GSK343 is a highly potent and selective EZH2 inhibitor with an IC50 of 4 nM. |
| R2032254 | MK-0752 | MK-0752 is a moderately potent γ-secretase inhibitor, which reduces Aβ40 product |
| R2032255 | Linsitinib(OSI906) | Linsitinib (OSI-906) is a dual inhibitor of the IGF-1 receptor and IR with IC50s |
