17 articles for RA Mantei
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Synthesis and In Vitro evaluation of fused ring heterocyle-containing angiotensin II antagonists.

TBA
Substituted 4-amino-1H-pyrazolo[3,4-d]pyrimidines as multi-targeted inhibitors of insulin-like growth factor-1 receptor (IGF1R) and members of ErbB-family receptor kinases.

Abbott Laboratories
Pyridone-containing farnesyltransferase inhibitors: synthesis and biological evaluation.

Abbott Laboratories
2,4-Diarylpyrrolidine-3-carboxylic acids--potent ETA selective endothelin receptor antagonists. 1. Discovery of A-127722.

Abbott Laboratories
Nonpeptide renin inhibitors with good intraduodenal bioavailability and efficacy in dog.

Abbott Laboratories
Discovery and optimization of novel constrained pyrrolopyridone BET family inhibitors.

Abbvie
Fragment-Based, Structure-Enabled Discovery of Novel Pyridones and Pyridone Macrocycles as Potent Bromodomain and Extra-Terminal Domain (BET) Family Bromodomain Inhibitors.

Abbvie
Methylpyrrole inhibitors of BET bromodomains.

Abbvie
C-terminal modifications of nonpeptide renin inhibitors: improved oral bioavailability via modification of physicochemical properties.

Abbott Laboratories
Discovery of N-(4-(2,4-Difluorophenoxy)-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)ethanesulfonamide (ABBV-075/Mivebresib), a Potent and Orally Available Bromodomain and Extraterminal Domain (BET) Family Bromodomain Inhibitor.

Abbvie
Substituted pyrrolidines as factor XIa inhibitors for the treatment thromboembolic diseases

Ono Pharmaceutical
HCV polymerase inhibitors

Medivir
Triazole compounds as KSP inhibitors

Novartis
Inhibitors

Probiodrug
Pharmacological characterization of human S1P4 using a novel radioligand, [4,5-3H]-dihydrosphingosine-1-phosphate.

Schering-Plough Research Institute
5HT4(a) and 5-HT4(b) receptors have nearly identical pharmacology and are both expressed in human atrium and ventricle.

University of Oslo
Structure-activity relationships of carbocyclic influenza neuraminidase inhibitors

Gilead Sciences