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30 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Discovery of furan-2-carbohydrazides as orally active glucagon receptor antagonists.EBI
Dainippon Sumitomo Pharma
Discovery of N-substituted 7-azaindoline derivatives as potent, orally available M1 and M4 muscarinic acetylcholine receptors selective agonists.EBI
Dainippon Sumitomo Pharma
Crystal Structures and Structure-Activity Relationships of Imidazothiazole Derivatives as IDO1 Inhibitors.EBI
Dainippon Sumitomo Pharma
Discovery of N-sulfonyl-7-azaindoline derivatives as potent, orally available and selective M(4) muscarinic acetylcholine receptor agonists.EBI
Dainippon Sumitomo Pharma
Structure-based optimization of cyclopropyl urea derivatives as potent soluble epoxide hydrolase inhibitors for potential decrease of renal injury without hypotensive action.EBI
Dainippon Sumitomo Pharma
Identification of a novel benzoxazolone derivative as a selective, orally active 18 kDa translocator protein (TSPO) ligand.EBI
Dainippon Sumitomo Pharma
7-Phenyl-imidazoquinolin-4(5H)-one derivatives as selective and orally available mPGES-1 inhibitors.EBI
Dainippon Sumitomo Pharma
Synthesis and biological evaluation of substituted imidazoquinoline derivatives as mPGES-1 inhibitors.EBI
Dainippon Sumitomo Pharma
Design, synthesis and structure-activity relationship of novel tricyclic benzimidazolone derivatives as potent 18 kDa translocator protein (TSPO) ligands.EBI
Dainippon Sumitomo Pharma
Discovery of novel N-substituted oxindoles as selective m1 and m4 muscarinic acetylcholine receptors partial agonists.EBI
Dainippon Sumitomo Pharma
Synthesis and evaluation of 8-oxoadenine derivatives as potent Toll-like receptor 7 agonists with high water solubility.EBI
Dainippon Sumitomo Pharma
Design, synthesis and structure-activity relationships of novel benzoxazolone derivatives as 18 kDa translocator protein (TSPO) ligands.EBI
Dainippon Sumitomo Pharma
Discovery of 3H-imidazo[4,5-c]quinolin-4(5H)-ones as potent and selective dipeptidyl peptidase IV (DPP-4) inhibitors.EBI
Dainippon Sumitomo Pharma
A practical use of ligand efficiency indices out of the fragment-based approach: ligand efficiency-guided lead identification of soluble epoxide hydrolase inhibitors.EBI
Dainippon Sumitomo Pharma
Synthesis and SAR study of imidazoquinolines as a novel structural class of microsomal prostaglandin E2 synthase-1 inhibitors.EBI
Dainippon Sumitomo Pharma
2-({6-[(3R)-3-amino-3-methylpiperidine-1-yl]-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-5H-pyrrolo[3,2-d]pyrimidine-5-yl}methyl)-4-fluorobenzonitrile (DSR-12727): a potent, orally active dipeptidyl peptidase IV inhibitor without mechanism-based inactivation of CYP3A.EBI
Dainippon Sumitomo Pharma
Synthesis and structure-activity relationship of tricyclic carboxylic acids as novel anti-histamines.EBI
Dainippon Sumitomo Pharma
Synthesis and pharmacological evaluation of novel benzoylazole-based PPARa/κ activators.EBI
Dainippon Sumitomo Pharma
Development of a new class of benzoylpyrrole-based PPARa/¿ activators.EBI
Dainippon Sumitomo Pharma
Discovery of new chemotype dipeptidyl peptidase IV inhibitors having (R)-3-amino-3-methyl piperidine as a pharmacophore.EBI
Dainippon Sumitomo Pharma
5,6,7,8-Tetrahydropyrido[4,3-d]pyrimidines as novel class of potent and highly selective CaMKII inhibitors.EBI
Dainippon Sumitomo Pharma
A novel class of antihyperlipidemic agents with low density lipoprotein receptor up-regulation via the adaptor protein autosomal recessive hypercholesterolemia.EBI
Dainippon Sumitomo Pharma
Synthesis and biological evaluation of 8-oxoadenine derivatives as toll-like receptor 7 agonists introducing the antedrug concept.EBI
Dainippon Sumitomo Pharma
Synthesis and structure-activity relationships of N-(4-amino-2,6-diisopropylphenyl)-N'-(1,4-diarylpiperidine-4-yl)methylureas as anti-hyperlipidemic agents.EBI
Dainippon Sumitomo Pharma
Novel 1,4-diarylpiperidine-4-methylureas as anti-hyperlipidemic agents: dual effectors on acyl-CoA:cholesterol O-acyltransferase and low-density lipoprotein receptor expression.EBI
Dainippon Sumitomo Pharma
Identification of 2,3-disubstituted pyridines as potent, non-emetic PDE4 inhibitors.EBI
Dainippon Sumitomo Pharma
Identification of N-substituted 8-azatetrahydroquinolone derivatives as selective and orally active M(1) and M(4) muscarinic acetylcholine receptors agonists.EBI
Dainippon Sumitomo Pharma
Structure-activity relationships of novel HIV-1 protease inhibitors containing the 3-amino-2-chlorobenzoyl-allophenylnorstatine structure.EBI
Dainippon Sumitomo Pharma
RAF kinase modulator compounds and methods of use thereofBDB
Ambit Biosciences