PMID
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Article Title
Organization
Orally active PDE4 inhibitors with therapeutic potential.

Minase Research Institute
New orally active PDE4 inhibitors with therapeutic potential.

Minase Research Institute
Highly potent PDE4 inhibitors with therapeutic potential.

Minase Research Institute
Synthesis and evaluation of¿-lactam analogs of PGE2 as EP4 and EP2/EP4 agonists.

Minase Research Institute
Discovery of orally available spirodiketopiperazine-based CCR5 antagonists.

Minase Research Institute
Discovery of long-acting N-(cyanomethyl)-N-alkyl-L-prolinamide inhibitors of dipeptidyl peptidase IV.

Minase Research Institute
Discovery of new chemical leads for prostaglandin D2 receptor antagonists.

Minase Research Institute
Discovery of novel prostaglandin analogs as potent and selective EP2/EP4 dual agonists.

Minase Research Institute
Pyrrolo[1,2-b]pyridazines, pyrrolo[2,1-f]triazin-4(3H)-ones, and related compounds as novel corticotropin-releasing factor 1 (CRF¿?) receptor antagonists.

Minase Research Institute
Discovery of a novel EP2/EP4 dual agonist with high subtype-selectivity.

Minase Research Institute
Synthesis and evaluation of novel modified¿-lactam prostanoids as EP4 subtype-selective agonists.

Minase Research Institute
Pyrazolo[1,5-a]pyrimidines, triazolo[1,5-a]pyrimidines and their tricyclic derivatives as corticotropin-releasing factor 1 (CRF¿?) receptor antagonists.

Minase Research Institute
Design and synthesis of new prostaglandin D2 receptor antagonists.

Minase Research Institute
6,7-Dihydro-5H-cyclopenta[d]pyrazolo[1,5-a]pyrimidines and their derivatives as novel corticotropin-releasing factor 1 receptor antagonists.

Minase Research Institute
Discovery of selective indole-based prostaglandin D2 receptor antagonist.

Minase Research Institute
3-(2-Aminocarbonylphenyl)propanoic acid analogs as potent and selective EP3 receptor antagonists. Part 3: Synthesis, metabolic stability, and biological evaluation of optically active analogs.

Minase Research Institute
Discovery of novel N-acylsulfonamide analogs as potent and selective EP3 receptor antagonists.

Minase Research Institute
3-(2-Aminocarbonylphenyl)propanoic acid analogs as potent and selective EP3 receptor antagonists. Part 1: discovery and exploration of the carboxyamide side chain.

Minase Research Institute
3-(2-Aminocarbonylphenyl)propanoic acid analogs as potent and selective EP3 receptor antagonists. part 2: optimization of the side chains to improve in vitro and in vivo potencies.

Minase Research Institute
Spirodiketopiperazine-based CCR5 antagonists: Improvement of their pharmacokinetic profiles.

Minase Research Institute
Design and synthesis of new potent dipeptidyl peptidase IV inhibitors with enhanced ex vivo duration.

Minase Research Institute
Design and synthesis of long-acting inhibitors of dipeptidyl peptidase IV.

Minase Research Institute
Discovery of orally active prostaglandin D2 receptor antagonists.

Minase Research Institute
Clarification of mechanism of human sputum elastase inhibition by a new inhibitor, ONO-5046, using electrospray ionization mass spectrometry.

Minase Research Institute
L-Cysteine based N-type calcium channel blockers: structure-activity relationships of the C-terminal lipophilic moiety, and oral analgesic efficacy in rat pain models.

Minase Research Institute
Structure-activity study of L-cysteine-based N-type calcium channel blockers: optimization of N- and C-terminal substituents.

Minase Research Institute
Design and synthesis of a highly selective EP4-receptor agonist. Part 2: 5-thia and 9beta-haloPG derivatives with improved stability.

Minase Research Institute
Design and synthesis of a highly selective EP4-receptor agonist. Part 1: 3,7-dithiaPG derivatives with high selectivity.

Minase Research Institute
Design and synthesis of a highly selective EP2-receptor agonist.

Minase Research Institute
New orally active serine protease inhibitors.

Minase Research Institute