17 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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3,4-dihydro-2(1H)-quinolinone as a novel antidepressant drug: synthesis and pharmacology of 1-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-3,4- dihydro-5-methoxy-2(1H)-quinolinone and its derivatives.

Otsuka Pharmaceutical
Characterization of orally active nonpeptide vasopressin V(2) receptor agonist. Synthesis and biological evaluation of both the (5R)- and (5S)-enantioisomers of 2-[1-(2-Chloro-4-pyrrolidin-1-yl-benzoyl)-2,3,4,5-tetrahydro-1H-1-benzazepin- 5-yl]-N-isopropylacetamide.

Otsuka Pharmaceutical
Novel design of nonpeptide AVP V(2) receptor agonists: structural requirements for an agonist having 1-(4-aminobenzoyl)-2,3,4, 5-tetrahydro-1H-1-benzazepine as a template.

Otsuka Pharmaceutical
Orally active, nonpeptide vasopressin V2 receptor antagonists: a novel series of 1-[4-(benzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepines and related compounds.

Otsuka Pharmaceutical
Orally active, nonpeptide vasopressin V1 antagonists. A novel series of 1-(1-substituted 4-piperidyl)-3,4-dihdyro-2(1H)-quinolinone.

Otsuka Pharmaceutical
5-[[4-[[morpholin-2-yl]methylamino]-5-(trifluoromethyl)-2 Pyridyl]Amino]Pyrazine-2-carbonitrile and therapeutic uses thereof

Cancer Research Technology
Substituted benzofuran, benzopyrrole, benzothiophene, and structurally related complement inhibitors

Biocryst Pharmaceuticals
Heterocyclic compounds for the inhibition of PASK

Bioenergenix
PARG inhibitory compounds

Cancer Research Technology
Methods, compositions, and uses of novel Fyn kinase inhibitors

Pathways Neuro Pharma
Negative allosteric modulators of metabotropic glutamate receptor 3

Vanderbilt University
Substituted 2,3,4,5,7,9,13,13a-octahydropyrido[1′,2′:4,5]pyrazino[2,1-b][1,3]OXAZEPINES and methods for treating viral infections

Gilead Sciences
Partially saturated nitrogen-containing heterocyclic compound

Taisho Pharmaceutical
The discovery of novel β-secretase inhibitors: pharmacophore modeling, virtual screening, and docking studies.

Peking University Health Science Center
The interaction of the enantiomers of aceclidine with subtypes of the muscarinic receptor.

University of California