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Cat.No. Product name Product Description
R2032379 CNX1351 CNX-1351 is a potent and isoform-selective targeted covalent PI3Kα inhibitor wit
R2032380 CP466722;Crenolanib CP-466722 is a rapidly reversible inhibitor of ATM, with an IC50 of 4.1 μM, and
R2032381 CP868596 Crenolanib is a potent and selective inhibitor of wild-type and mutant isoforms
R2032382 Devimistat(CPI-613) Devimistat (CPI-613) is a lipoic acid analog that inhibits pyruvate dehydrogenas
R2032383 Fimepinostat(CUDC-907) Fimepinostat (CUDC-907) potently inhibits class I PI3Ks as well as classes I and
R2032384 CX5461 CX-5461 is a potent and oral rRNA synthesis inhibitor.It inhibits RNA polymerase
R2032385 CX-6258 CX-6258 is a potent and kinase selective pan-Pim kinases inhibitor, with IC50s o
R2032386 CZC24832 CZC24832 is a highly selective and potent PI3Kγ inhibitor (IC50=27 nM) with appa
R2032387 Dalcetrapib(JTT-705;RO4607381) Dalcetrapib (JTT-705; RO-4607381) is a rhCETP inhibitor with IC50 of 0.2 μM that
R2032388 Dasabuvir(ABT-333) Dasabuvir (ABT-333) is a nonnucleoside inhibitor of the RNA-dependent RNA polyme
R2032389 DCC-2036(Rebastinib) Rebastinib (DCC-2036) is a conformational control Bcr-Abl inhibitor for Abl1WT a
R2032390 c-Kit-IN-1 c-Kit-IN-1 is a potent inhibitor of c-Kit and c-Met with IC50s of <200 nM.
R2032391 Degrasyn(WP1130) Degrasyn (WP1130) is a cell-permeable deubiquitinase (DUB) inhibitor, directly i
R2032392 ELN441958 ELN-441958 is a potent, neutral antagonist of B1 receptor, inhibits the binding
R2032393 ENMD-2076 ENMD-2076 is a multi-targeted kinase inhibitor with IC50s of 1.86, 14, 58.2, 15.
R2032394 EPZ004777 EPZ004777 is a potent, selective DOT1L inhibitor with an IC50 of 0.4 nM.
R2032395 EPZ005687 EPZ005687 is a potent and selective inhibitor of EZH2 with Ki of 24 nM, and has
R2032396 Pinometostat(EPZ-5676) Pinometostat (EPZ-5676) is a potent DOT1L histone methyltransferase inhibitor wi
R2032397 ETP46464 ETP-46464 is an effective mTOR and ATR inhibitor with IC50s of 0.6 and 14 nM, re
R2032398 FR 180204 FR 180204 is an ATP-competitive and selective ERK inhibitor.FR 180204 inhibits E
R2032399 GNE-0877 GNE0877 is a highly potent, selective, and brain-penetrant aminopyrazole leucine
R2032400 GNE-477 GNE-477 is a potent and efficacious dual PI3K (IC50=4 nM)/mTOR(Ki=21 nM) inhibit
R2032401 GNE7915 GNE-7915 is a potent, selective and brain-penetrant inhibitor of LRRK2 with an I
R2032402 GNE9605 GNE-9605 is a highly potent, selective, and brain-penetrant LRRK2 inhibitor with
R2032403 GNF-5 GNF-5, an analogue of GNF-2 with improved pharmacokinetic properties, is a selec
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