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Cat.No. Product name Product Description
R10663 5SrRNAmodificator
R10664 CM 346; Obenoxazine HCl CM 346 is an anxiolytic drug, produces anxiolytic and neuroprotective effects wi
R10667 GBR12935 Dihydrochloride GBR 12935 dihydrochloride inhibits DAT (dopamine transporter) (Ki = 21.5 nM) and
R10672 LH846 LH846 is a selective inhibitor of CK1δ (IC50 values are 290 nM, 1.3 uM and 2.5 u
R10675 B-RafIN1 B-Raf IN 1 is a highlt potent and selective B-Raf inhibitor with IC50 of 24 nM;
R10678 ZLN005 ZLN005 is a potent and tissue-specific PGC-1α transcriptional activator.
R10679 kobe2602 kobe2602 is a novel and effective small-molecule compound inhibiting Ras–Raf int
R10685 Nimorazole Nimorazole is a nitroimidazole anti-infective. It is also being investigated for
R10686 LB-100 LB-100 is a water soluble protein phosphatase 2A (PP2A) inhibitor. Phase 1.
R10689 ISRIB ISRIB (trans-isomer) is a potent and selective small molecule inhibitor of PERK
R10690 Clemizole.HCl Clemizole hydrochloride is an antagonist of H1 histamine receptor with an IC50 v
R10691 1443139-14-7
R10693 Nicaraven Nicaraven is a hydroxyl radical scavenger with antivasospastic and neuroprotecti
R10694 1350920-22-7
R10695 Bioymifi (DR5 Activator) Bioymifi is a potent and selective small molecule agonist of DR5 that directly t
R10696 2-Chloro-N-[[2'-[(cyanoamino)sulfonyl][1,1'-biphenyl]-4-yl]methyl]-N-[(4-methylphenyl)methyl]-benzamide S0859, an N-cyanosulphonamide compound, reversibly inhibit NBC-mediated pH(i) re
R10704 SRPIN340 SRPIN340 is a selective SRPK inhibitor with Ki of 0.89 μM for SRPK1, showing no
R10718 kbNB142-70 kb NB 142-70 is a selective protein kinase D (PKD) inhibitor (IC50 values are 28
R10719 APY0201 APY0201 is a potent, highly selective, ATP-competitive PIKfyve inhibitor (IC50=5
R10721 ACT058362; Palosuran Palosuran is a new potent and specific antagonist of the human UT receptor with
R10722 CASIN CASIN is a selective GTPase Cdc42 inhibitor with IC50 of 2 uM. In vitro: Treatme
R10728 BVT2733 BVT 2733 is a new, small molecule, non-steroidal, isoform-selective inhibitor of
R10730 NSC-41589
R10731 SKLB477;FLT3-​IN-​1 SKLB4771 is a novel potent and selective Flt3 inhibitor with IC50 of 10 nM; agai
R10734 TH588 TH588 is a potent and selective MTH1 (NUDT1) inhibitor with IC50 of 5 nM.
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