16 articles for WM Moore
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Cmpds
Data
Article Title
Organization
26
Discovery and SAR of PF-4693627, a potent, selective and orally bioavailable mPGES-1 inhibitor for the potential treatment of inflammation.

Pfizer
19
Synthesis and biological evaluation of substituted benzoxazoles as inhibitors of mPGES-1: use of a conformation-based hypothesis to facilitate compound design.

Pfizer
28
Novel benzoxazole inhibitors of mPGES-1.

Pfizer
7
5-Fluorinated L-lysine analogues as selective induced nitric oxide synthase inhibitors.

Pfizer
2
Synthesis and biological characterization of L-N(6)-(1-iminoethyl)lysine 5-tetrazole-amide, a prodrug of a selective iNOS inhibitor.

Pfizer
10
2-Iminohomopiperidinium salts as selective inhibitors of inducible nitric oxide synthase (iNOS).

Pfizer
14
2-Iminopyrrolidines as potent and selective inhibitors of human inducible nitric oxide synthase.

Pfizer
11
2-Iminopiperidine and other 2-iminoazaheterocycles as potent inhibitors of human nitric oxide synthase isoforms.

G. D. Searle Research and Development
6
L-N6-(1-iminoethyl)lysine: a selective inhibitor of inducible nitric oxide synthase.

G. D. Searle Research and Development
7
Phosphorus-containing inhibitors of endothelin converting enzyme: effects of the electronic nature of phosphorus on inhibitor potency.

Monsanto
11
Thiol and hydroxamic acid containing inhibitors of endothelin converting enzyme

TBA
5
3-Hydroxy-4-methyl-5-pentyl-2-iminopyrrolidine: a potent and highly selective inducible nitric oxide synthase inhibitor.

Pharmacia
14
Selective heterocyclic amidine inhibitors of human inducible nitric oxide synthase.

Pharmacia
2
Acetamidine lysine derivative, N-(5(S)-amino-6,7-dihydroxyheptyl)ethanimidamide dihydrochloride: a highly selective inhibitor of human inducible nitric oxide synthase.

Searle
18
Substituted 2-iminopiperidines as inhibitors of human nitric oxide synthase isoforms.

G. D. Searle Research and Development
4
Synthesis and evaluation of two positron-labeled nitric oxide synthase inhibitors, S-[11C]methylisothiourea and S-(2-[18F]fluoroethyl)isothiourea, as potential positron emission tomography tracers.

Washington University