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Cat. No. Product Name Field of Application Chemical Structure
DC7206 R1530 Featured R1530 is the multikinase inhibitor with potential antiangiogenesis and antineoplastic activities.
DC11138 Guanabenz acetate R15A inhibitor.
DC10692 R162 Featured R162 is an inhibitor of GDH activity and represses glioma cell growth.
DC22205 R191 R191 (R-191) is a potent, small molecule IRAK1/4 kinase inhibitor (IRAK4 IC50=3 nM), exhibits good selectivity against a broad panel of kinases.
DC22670 R243 Featured R243 is a potent, small molecule CCR8 antagonist that inhibits CCR8 signaling and chemotaxis, inhibits CCL1-induced Ca2+ flux and CCL1-driven peritoneal macrophages aggregation at 0.2 uM.
DC7037 R306465(JNJ-16241199) Featured R306465, also known as JNJ-16241199, is a novel hydroxamate-based histone deacetylase (HDAC) inhibitor with broad-spectrum antitumour activity against solid and haematological malignancies in preclinical models.
DC21551 R-360163 R-360163 is a small molecule inhibitor that effectively inhibits the β-catenin/Tcf4 interaction with Ki of 16 uM in FP assay.
DC1014 R406 free base Featured R406 is a potent Syk inhibitor with IC50 of 41 nM and also potently inhibits Flt3.
DC8733 R406 Featured R406 is a potent Syk inhibitor with IC50 of 41 nM and also potently inhibits Flt3.
DC7258 Bemcentinib(R428,BGB324) Featured R428 is a potent and selective small-molecule inhibitor(IC50=14 nM), blocks the activities of Axl.
DC2068 R547 R547 is a potent and selective CDK inhibitor with Ki and IC50 of 1-3 nM and 80 nM respectively.
DC10897 R-7050 Featured R-7050 is a tumor necrosis factor receptor (TNFR) antagonist with greater selectivity toward TNFα.
DC9462 R-7128(Mericitabine) Featured R-7128(Mericitabine) is a selective nucleoside analog inhibitor of the hepatitis C virus (HCV) NS5B RNA-dependent RNA polymerase, with activity across all HCV genotypes.
DC9841 Fostamatinib(R788) Featured R788 (Fostamatinib), a prodrug of the active metabolite R406, is a potent Syk inhibitor with IC50 of 41 nM.
DC10995 R916562 R916562 (R562) is a potent, dual Axl/VEGF-R2 inhibitor with celluar IC50 of 136 nM for Axl.
DC1013 R788 disodium (Fostamatinib) Featured R935788 (Fostamatinib disodium, R788) is a Syk inhibitor with IC50 of 41 nM.
DC21555 R-999636 R-999636 is a small molecule inhibitor that effectively inhibits the β-catenin/Tcf4 interaction with Ki of 8.8 uM in FP assay.
DC10304 RA190 Featured RA190, a bis-benzylidine piperidon, inhibits proteasome function by covalently binding to cysteine 88 of ubiquitin receptor RPN13.
DC9103 Rebeprazole sodium Rabeprazole sodium(LY307640 sodium) is an antiulcer drug in the class of proton pump inhibitors.
DC10578 rac BHFF Featured Rac BHFF is a potent and selective GABAB receptor positive allosteric modulator that increases the efficacy and potency of GABA ( > 149% and > 15-fold respectively). Orally active and exhibits anxiolytic activity in vivo.
DC21544 rac Pterosin B rac Pterosin B is a potent and specific SIK3 signaling inhibitor that suppresses SIK3 downstream cascades by up-regulating the phosphorylation levels in the SIK3 C-terminal regulatory domain.
DC9107 Racecadotril Featured Racecadotril (acetorphan), a potent enkephalinase inhibitor (IC50= 4.5 uM), protects endogenous enkephalins from degradation.
DC9657 RAD140 Featured RAD140 is a potent, orally bioavailable, nonsteroidal selective androgen receptor modulator (SARM).
DC20528 RAD51-IN-1 Featured RAD51-IN-17 is a quinazolinone derivative that inhibts homologous recombinase RAD51, effectively inhibits both RAD51 foci formation in response to DNA damage, and proliferation of TNBC cell lines.
DC9513 Radafaxine (hydrochloride) Featured Radafaxine Hcl(BW-306U; GW-353162A) is a potent metabolite of bupropion; selective for inhibiting the reuptake of norepinephrine over dopamine; DAT (dopamine transporter) and NET(norepinephrine transporter) transporters inhibitor, and nAChR family modulat
DC21069 Radalbuvir Radalbuvir (GS-9669) is a highly optimized thumb site II nonnucleoside inhibitor of HCV NS5B polymerase with binding affinity of 1.35 nM for genotype 1b.
DC9351 Radezolid Featured Radezolid (RX-1741) is a novel oxazolidinone antibiotic agent.
DC12701 Radiprodil Featured Radiprodil is an orally active and selective NMDA NR2B antagonist; a potential therapeutic agent in treatment of neuropathic pain and possibly other chronic pain conditions.
DC8011 Radotinib (IY-5511) Featured Radotinib(IY-5511) is a novel and selective BCR-ABL1 tyrosine kinase inhibitor with IC50 of 34 nM for wild-type BCR-ABL1 kinase.
DC5049 RAF265 (CHIR-265) Featured RAF265 (CHIR-265) is a highly selective B-Raf and VEGFR2 inhibitor with IC50 of 3-60 nM and EC50 of 30 nM, including B-Raf, C-Raf and mutant B-Raf.

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