The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
25654260 |
49 |
Discovery of highly selective brain-penetrant vasopressin 1a antagonists for the potential treatment of autism via a chemogenomic and scaffold hopping approach. |
F. Hoffmann-La Roche |
25642985 |
45 |
Selective nonpeptidic fluorescent ligands for oxytocin receptor: design, synthesis, and application to time-resolved FRET binding assay. |
University of Strasburg |
24874785 |
333 |
New, potent, and selective peptidic oxytocin receptor agonists. |
Ferring Research Institute |
16250654 |
41 |
2,5-diketopiperazines as potent, selective, and orally bioavailable oxytocin antagonists. 2. Synthesis, chirality, and pharmacokinetics. |
Glaxosmithkline |
21700453 |
56 |
Optimisation of pharmacokinetic properties to afford an orally bioavailable and selective V1A receptor antagonist. |
Msd |
21458261 |
55 |
The discovery of novel 8-azabicyclo[3.2.1]octan-3-yl)-3-(4-chlorophenyl) propanamides as vasopressin V1A receptor antagonists. |
Msd |
21146408 |
53 |
The characterization of a novel V1b antagonist lead series. |
Glaxosmithkline |
20674355 |
58 |
Pyrrolo[1,2-a]pyrazine and pyrazolo[1,5-a]pyrazine: novel, potent, and selective series of Vasopressin 1b receptor antagonists. |
Glaxosmithkline |
19081251 |
38 |
Discovery and optimisation of a potent and selective tertiary sulfonamide oxytocin antagonist. |
Glaxosmithkline |
22984902 |
59 |
Selective fluorescent nonpeptidic antagonists for vasopressin V2 GPCR: application to ligand screening and oligomerization assays. |
University of Strasburg |
22239250 |
59 |
Pyridyl-2,5-diketopiperazines as potent, selective, and orally bioavailable oxytocin antagonists: synthesis, pharmacokinetics, and in vivo potency. |
Glaxosmithkline |
22425346 |
28 |
Synthesis and evaluation of C-11, F-18 and I-125 small molecule radioligands for detecting oxytocin receptors. |
Emory University |
19800231 |
92 |
Tetrahydroquinoline sulfonamides as vasopressin 1b receptor antagonists. |
Schering-Plough Research Institute |
18032036 |
17 |
The discovery of GSK221149A: a potent and selective oxytocin antagonist. |
Glaxosmithkline |
17850055 |
18 |
Toward efficient drug screening by homogeneous assays based on the development of new fluorescent vasopressin and oxytocin receptor ligands. |
Institute Genomics Functional (Igf) |
17300166 |
88 |
Design and synthesis of the first selective agonists for the rat vasopressin V(1b) receptor: based on modifications of deamino-[Cys1]arginine vasopressin at positions 4 and 8. |
University of Montpellier |
16302826 |
129 |
Discovery and development of a new class of potent, selective, orally active oxytocin receptor antagonists. |
Serono Pharmaceutical Research Institute |
15084136 |
96 |
Design of potent and selective agonists for the human vasopressin V1b receptor based on modifications of [deamino-cys1]arginine vasopressin at position 4. |
Medical College of Ohio |
12036367 |
46 |
Synthesis and characterization of fluorescent antagonists and agonists for human oxytocin and vasopressin V(1)(a) receptors. |
University of Montpellier |
22249122 |
9 |
Synthesis and evaluation of potent and selective human V1a receptor antagonists as potential ligands for PET or SPECT imaging. |
Lehigh University |
21688787 |
295 |
New, potent, selective, and short-acting peptidic V1a receptor agonists. |
Ferring Research Institute |
21605973 |
69 |
Potent and selective oxindole-based vasopressin 1b receptor antagonists with improved pharmacokinetic properties. |
Abbott Laboratories |
21601454 |
26 |
Identification and optimisation of novel sulfonamide, selective vasopressin V1B receptor antagonists. |
Msd |
21596563 |
33 |
Synthesis and SAR studies of novel 2-(6-aminomethylaryl-2-aryl-4-oxo-quinazolin-3(4H)-yl)acetamide vasopressin V1b receptor antagonists. |
Msd |
21428295 |
43 |
Design, synthesis, and pharmacological characterization of fluorescent peptides for imaging human V1b vasopressin or oxytocin receptors. |
University of Montpellier |
21353540 |
55 |
Synthesis and SAR studies of novel 2-(4-oxo-2-aryl-quinazolin-3(4H)-yl)acetamide vasopressin V1b receptor antagonists. |
Msd |
20550119 |
96 |
Oral oxytocin antagonists. |
Drugmoldesign |
20719508 |
26 |
Identification and optimization of novel 2-(4-oxo-2-aryl-quinazolin-3(4H)-yl)acetamide vasopressin V3 (V1b) receptor antagonists. |
Ligand Pharmaceuticals |
18778939 |
23 |
Triazole oxytocin antagonists: identification of aryl ether replacements for a biaryl substituent. |
Pfizer |
12502367 |
17 |
New benzo[h][1,6]naphthyridine and azepino[3,2-c]quinoline derivatives as selective antagonists of 5-HT4 receptors: binding profile and pharmacological characterization. |
Université |
31022340 |
101 |
Discovery of Potent, Selective, and Short-Acting Peptidic V |
Ferring Research Institute |
30896946 |
36 |
Development of a Highly Potent Analogue and a Long-Acting Analogue of Oxytocin for the Treatment of Social Impairment-Like Behaviors. |
Tohoku University and Department of Pharmaceutical Sciences |
31229420 |
21 |
Synthesis of oxytocin derivatives lipidated via a carbonate or carbamate linkage as a long-acting therapeutic agent for social impairment-like behaviors. |
Kanazawa University |
10197974 |
22 |
Fluorescent pseudo-peptide linear vasopressin antagonists: design, synthesis, and applications. |
University of Montpellier |
31223461 |
56 |
Discovery of SHR1653, a Highly Potent and Selective OTR Antagonist with Improved Blood-Brain Barrier Penetration. |
Shanghai Hengrui Pharmaceutical |
31850759 |
24 |
Engineering a Potent, Long-Acting, and Periphery-Restricted Oxytocin Receptor Agonist with Anorexigenic and Body Weight Reducing Effects. |
Calibr At The Scripps Research Institute |
30098866 |
30 |
Novel, potent, selective and brain penetrant vasopressin 1b receptor antagonists. |
Abbvie Deutschland |
30199637 |
172 |
LIT-001, the First Nonpeptide Oxytocin Receptor Agonist that Improves Social Interaction in a Mouse Model of Autism. |
Umr7200 Cnrs/Universit£ |
29602673 |
49 |
Building bridges for highly selective, potent and stable oxytocin and vasopressin analogs. |
Imperial College |
17221184 |
55 |
Synthesis and in vivo evaluation of a novel 5-HT1A receptor agonist radioligand [O-methyl- 11C]2-(4-(4-(2-methoxyphenyl)piperazin-1-yl)butyl)-4-methyl-1,2,4-triazine-3,5(2H,4H)dione in nonhuman primates. |
Columbia University |
12660315 |
17 |
Pharmacology of (2S,4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4-(methoxyimino) -1-[(2'-methyl[1,1'-biphenyl]-4-yl)carbonyl]-2-pyrrolidinecarboxamide, a new potent and selective nonpeptide antagonist of the oxytocin receptor. |
Lcg Bioscience |
12649361 |
779 |
L-homocysteine sulfinic acid and other acidic homocysteine derivatives are potent and selective metabotropic glutamate receptor agonists. |
Case Western Reserve University |
12192085 |
52 |
Salvinorin A: a potent naturally occurring nonnitrogenous kappa opioid selective agonist. |
Case Western Reserve University |
12110997 |
380 |
In vitro receptor screening of pure constituents of St. John's wort reveals novel interactions with a number of GPCRs. |
WestfÄLische Wilhelms-UniversitÄ |
11861823 |
10 |
Characterization of (2S,4R)-1-[5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-N,N-dimethyl-2-pyrrolidine carboxamide (SSR149415), a selective and orally active vasopressin V1b receptor antagonist. |
Sanofi-Synthelabo Recherche |
11512051 |
80 |
The in vitro pharmacology of the beta-adrenergic receptor pet ligand (s)-fluorocarazolol reveals high affinity for cloned beta-adrenergic receptors and moderate affinity for the human 5-HT1A receptor. |
Case Western Reserve University |
9864265 |
14 |
OPC-41061, a highly potent human vasopressin V2-receptor antagonist: pharmacological profile and aquaretic effect by single and multiple oral dosing in rats. |
Second Tokushima Institute of New Drug Research |
9454810 |
72 |
SR 144528, the first potent and selective antagonist of the CB2 cannabinoid receptor. |
Sanofi Recherche |
9223568 |
38 |
Pharmacological profile of YM087, a novel potent nonpeptide vasopressin V1A and V2 receptor antagonist, in vitro and in vivo. |
Yamanouchi Pharmaceutical |