16 articles for KA Faust
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Potent, orally active imidazo[4,5-b]pyridine-based angiotensin II receptor antagonists.

Exploratory Chemistry Merck Sharp and Dohme Research Laboratories
AT
1 selective angiotensin II antagonists with phenoxyphenylacetic acid as a biphenyl replacement part I

TBA
The SAR of 6-(N-alkyl-N-acyl)-2-propyl-3-[(2′-tetrazol-5-yl)biphen-4-yl)methyl]-quinazolinones as balanced affinity antagonists of the human AT
1 and AT
2 receptors

TBA
α-Phenoxyphenylacetic acid derived angiotensin II antagonists with low nanomolar AT
1/AT
2 receptor subtype affinity (Part II)

TBA
Development of angiotensin II antagonists with equipotent affinity for human AT
1 and AT
2 receptor subtypes.

TBA
A new class of balanced AT
1/AT
2 angiotensin II antagonists: quinazolinone AII antagonists with acylsulfonamide and sulfonylcarbamate acidic functionalities

TBA
Potent imidazole angiotensinII antagonists: acyl sulfonamides and acyl sulfamides as tetrazole replacements

TBA
Triazolinones as nonpeptide angiotensin II antagonists. 2. discovery of a potent and orally active triazolinone acylsulfonamide

TBA
Quinazolinones 2: QSAR and in vivo characterization of AT1 selective AII antagonists

TBA
Quinazolinones 1: design and synthesis of potent quinazolinone- containing AT
1-selective angiotensin-II receptor antagonists

TBA
Nonpeptide angiotensin II antagonists derived from 4H-1,2,4-triazoles and 3H-imidazo[1,2-b][1,2,4]triazoles.

Merck Research Laboratories
Triazolinones as nonpeptide angiotensin II antagonists. 1. Synthesis and evaluation of potent 2,4,5-trisubstituted triazolinones.

Merck Research Laboratories
Nonpeptide angiotensin II antagonists derived from 1H-pyrazole-5-carboxylates and 4-aryl-1H-imidazole-5-carboxylates.

Merck Research Laboratories
A potent, orally active, balanced affinity angiotensin II AT1 antagonist and AT2 binding inhibitor.

Merck Research Laboratories
Triazolinone biphenylsulfonamide derivatives as orally active angiotensin II antagonists with potent AT1 receptor affinity and enhanced AT2 affinity.

Merck Research Laboratories
A highly potent, orally active imidazo[4,5-b]pyridine biphenylacylsulfonamide (MK-996; L-159,282): a new AT1-selective angiotensin II receptor antagonist.

Merck Research Laboratories