14 articles for JS Wai
The following articles (labelled with PubMed ID or TBD) are for your review
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Synthesis and evaluation of 2-pyridinone derivatives as HIV-1-specific reverse transcriptase inhibitors. 4. 3-[2-(Benzoxazol-2-yl)ethyl]-5-ethyl-6-methylpyridin-2(1H)-one and analogues.

Merck Reserch Laboratories
A series of 5-aminosubstituted 4-fluorobenzyl-8-hydroxy-[1,6]naphthyridine-7-carboxamide HIV-1 integrase inhibitors.

Merck Research Laboratories
A series of 5-(5,6)-dihydrouracil substituted 8-hydroxy-[1,6]naphthyridine-7-carboxylic acid 4-fluorobenzylamide inhibitors of HIV-1 integrase and viral replication in cells.

Merck Research Laboratories
Design and synthesis of 8-hydroxy-[1,6]naphthyridines as novel inhibitors of HIV-1 integrase in vitro and in infected cells.

Merck Research Laboratories
4-Aryl-2,4-dioxobutanoic acid inhibitors of HIV-1 integrase and viral replication in cells.

Merck Research Laboratories
Nonpeptide GPIIB/IIIA receptor antagonists. Part 21: C-6 flexibility and amide bond orientation are important factors in determining the affinity of compounds for activated or resting platelet receptors.

Merck Research Laboratories
Potent and selective HIV-1 ribonuclease H inhibitors based on a 1-hydroxy-1,8-naphthyridin-2(1H)-one scaffold.

Merck And
8-Hydroxy-3,4-dihydropyrrolo[1,2-a]pyrazine-1(2H)-one HIV-1 integrase inhibitors.

Merck Research Laboratories
Dihydroxypyridopyrazine-1,6-dione HIV-1 integrase inhibitors.

Merck Research Laboratories
7-hydroxy-indolinyl antagonists of P2Y1 receptor

Bristol-Myers Squibb
5-fluoro-N-(pyridin-2-yl)pyridin-2-amine derivatives containing a sulfone group

Bayer Pharma Aktiengesellschaft
Cyclosporin analogues for preventing or treating hepatitis C infection

Enanta Pharmaceuticals
Substituted condensed pyrimidine compounds

GrÜNenthal
Macrocyclic urea and sulfamide derivatives as inhibitors of TAFIa

Sanofi