15 articles for TJ Opgenorth
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
Potent and selective inhibitors of an aspartyl protease-like endothelin converting enzyme identified in rat lung.

Abbott Laboratories
Pharmacology of A-216546: a highly selective antagonist for endothelin ET(A) receptor.

Abbott Laboratories
Pharmacology of endothelin receptor antagonists ABT-627, ABT-546, A-182086 and A-192621: in vitro studies.

Abbott Laboratories
Pyrrolidine-3-carboxylic acids as endothelin antagonists. 5. Highly selective, potent, and orally active ET(A) antagonists.

Abbott Laboratories
Design, synthesis, and activity of a series of pyrrolidine-3-carboxylic acid-based, highly specific, orally active ET(B) antagonists containing a diphenylmethylamine acetamide side chain.

Abbott Laboratories
Pyrrolidine-3-carboxylic acids as endothelin antagonists. 4. Side chain conformational restriction leads to ET(B) selectivity.

Abbott Laboratories
Pyrrolidine-3-carboxylic acids as endothelin antagonists. 3. Discovery of a potent, 2-nonaryl, highly selective ETA antagonist (A-216546).

Abbott Laboratories
Pyrrolidine-3-carboxylic acids as endothelin antagonists. 2. Sulfonamide-based ETA/ETB mixed antagonists.

Abbott Laboratories
Potent and selective non-benzodioxole-containing endothelin-A receptor antagonists.

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

Abbott Laboratories
Azole endothelin antagonists. 3. Using delta log P as a tool to improve absorption.

Abbott Laboratories
Azole endothelin antagonists. 2. Structure-activity studies.

Abbott Laboratories
Azole endothelin antagonists. 1. A receptor model explains an unusual structure-activity profile.

Abbott Laboratories