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Cat.No. Product name Product Description
R10001 R788; Fostamatinib Fostamatinib (R788), a prodrug of the active metabolite R406, is a Syk inhibitor
R10002 R406 Free base R406 (free base) is a potent Syk inhibitor with IC50 of 41 nM in a cell-free ass
R10003 Infigratinib (Synonyms: BGJ-398; NVP-BGJ398) BGJ398 (NVP-BGJ398) is a potent and selective FGFR inhibitor for FGFR1/2/3 with
R10004 VX-809; Lumacaftor VX-809 (Lumacaftor) acts to correct CFTR mutations common in cystic fibrosis by
R10005 AT406 (SM-406, ARRY-334543) AT-406 is an orally bioavailable inhibitor of IAP family of proteins with potent
R10006 Allitinib tosylate (Synonyms: AST-1306 (TsOH))/897383-62-9 Free base AST-1306 is a novel irreversible inhibitor of EGFR and ErbB2 with IC50 of 0.5 nM
R10007 AZD6244 Selumetinib (AZD6244) is a potent, highly selective MEK1 inhibitor with IC50 of
R10008 Rucaparib phosphate; AG014699; PF01367388 Rucaparib (AG-014699, PF-01367338) is an inhibitor of PARP with Ki of 1.4 nM for
R10009 AZD8055 AZD8055 is a novel ATP-competitive mTOR inhibitor with IC50 of 0.8 nM in MDA-MB-
R10010 Rucaparib; AG-014699; PF-01367388 Rucaparib (AG-014699, PF-01367338) is an inhibitor of PARP with Ki of 1.4 nM for
R10011 BIO-acetoxime; GSK3 Inhibitor IX BIO-acetoxime is a potent dual GSK3α/β inhibitor with IC50 of 10 nM, >240-fol
R10012 NVP-HSP990 (HSP990) NVP-HSP990 (HSP990) is a novel, potent and selective HSP90 inhibitor for HSP90α/
R10013 PF 04691502 PF-04691502 is an ATP-competitive PI3K(α/β/δ/γ)/mTOR dual inhibitor with Ki of 1
R10014 AKT inhibitor VIII (AKTI-1/2) CAS NO.:612847-09-3Product Name:1-(1-(4-(6-Phenyl-1H-imidazo[4,5-g]quinoxalin-7-
R10015 MN-64 MN-64 is a inhibitor of tankyrases, showed 6 nM potency against tankyrase 1, iso
R10016 TH287 TH287 is a potent and selective MTH1 (NUDT1) inhibitor with IC50 of 0.8 nM.
R10019 Setanaxib (Synonyms: GKT137831; GKT831) Setanaxib (GKT137831) is a selective NADPH oxidase (NOX1/4) inhibitor with Kis o
R10020 JNJ-31020028 JNJ-31020028 is a selective brain penetrant antagonist of neuropeptide Y2 recept
R10022 GSK429286A GSK429286A is a selective inhibitor of ROCK1 and ROCK2 with IC50 of 14 nM and 63
R10024 Cardiogenol C hydrochloride Cardiogenol C hydrochloride is a cell-permeable pyrimidine compound which potent
R10025 MLN2238 MLN2238 inhibits the chymotrypsin-like proteolytic (β5) site of the 20S proteaso
R10026 Ruxolitinib (INCB018424) CAS NO.:941678-49-5Product Name:β-Cyclopentyl-4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl
R10027 KU-0063794 KU-0063794 is a potent and highly specific dual-mTOR inhibitor of mTORC1 and mTO
R10028 MLN9708 MLN9708 immediately hydrolyzed to MLN2238, the biologically active form, on expo
R10029 ML141 (CID-2950007) ML141 is a potent, selective and reversible non-competitive inhibitor of Rho fam
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