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| Cat.No. | Product name | Product Description |
| R11362 | Isoxicam | N/A |
| R11363 | Enzastaurin;LY317615 | Enzastaurin is a potent and selective PKCβ inhibitor with an IC50 of 6 nM, showi |
| R11364 | GNE-493 | GNE-493 is a potent, selective, and orally available dual pan-PI3-kinase/mTOR in |
| R11366 | Capromorelin Tartrate (Synonyms: CP 424391-18) | Capromorelin Tartrate is an orally active, potent growth hormone secretagogue re |
| R11367 | Altiratinib (Synonyms: DCC-2701) | Altiratinib (DCC-2701) is a multi-targeted kinase inhibitor with IC50s of 2.7, 8 |
| R11374 | Bay 59-3074 | Bay 59-3074 is a selective cannabinoid CB1/CB2 receptor partial agonist with Ki |
| R11375 | Rapastinel;GLYX-13 | Rapastinel (GLYX-13) is an N-methyl-D-aspartate receptor (NMDAR) modulator that |
| R11376 | GDC0152 | GDC-0152 is a potent IAPs inhibitor, and binds to the BIR3 domains of XIAP, cIAP |
| R11377 | Raltegravir intermediates | N/A |
| R11378 | Donepezil Hydrochloride;E2020 | Donepezil (Hydrochloride) (E-2020) is a noncompetitive acetylcholinesterase inhi |
| R11379 | PLX7904 | PLX7904 is a potent and selective BRAF inhibitor, with IC50 of appr 5 nM against |
| R11380 | ACP196;acalabrutinib | Acalabrutinib is an orally active, irreversible, and highly selective BTK inhibi |
| R11381 | Ap26113; brigatinib | Brigatinib is a highly potent and selective ALK inhibitor, with an IC50 of 0.6 n |
| R11382 | EAI-045;EAI045 | EAI045 is an allosteric and the fourth-generation inhibitor of mutant EGFR& |
| R11383 | Olmutinib (Synonyms: HM61713, BI 1482694) | Olmutinib (HM61713; BI-1482694) is an orally bioavailab and irreversible third E |
| R11386 | Cladribine | N/A |
| R11389 | Mivebresib (Synonyms: ABBV-075) | Mivebresib is a potent and orally available bromodomain and extraterminal domain |
| R11390 | Madrasin (DDD00107587) | Madrasin (DDD00107587) is a splicing inhibitor that prevents formation of both s |
| R11391 | MK-571;MK571 | MK-571 is a selective, orally active leukotriene D4 receptor antagonist, with Ki |
| R11392 | (E)-SIS3 | (E)-SIS3 is a specific, cell-permeable, and selective Smad3 inhibitor, which inh |
| R11393 | Odanacatib;MK-0822 | Odanacatib (MK-0822) is a potent and selective inhibitor of cathepsin K, with an |
| R11395 | WIN35428 | (–)-2-β-Carbomethoxy-3-β-(4-fluorophenyl)tropane (β-CFT, WIN 35,428) is a stimul |
| R11397 | BM212 | BM212 exerts bactericidal activity against intracellular bacilli residing, compl |
| R11398 | SKF96365 HCl | SKF-96365 hydrochloride is a non-selective TRP Channel blocker. |
| R11400 | MK-5172 intermediates 1 | N/A |
