DC7206 |
R1530
Featured
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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. |
|