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Guy Falardeau

Research Profile

Chemicals & Drugs

Living Beings

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Drug Design

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Microbial Sensitivity Tests

Anatomy

Cell Line

Phenomena

Hydrogen Bonding

Physiology

Amino Acid Substitution

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Publications

TOP 3
Guy Falardeau; Hugo Lachance; Annie St-Pierre; Constantin G Yannopoulos; Marc Drouin; Jean Bédard; Laval Chan
Design and synthesis of a potent macrocyclic 1,6-naphthyridine anti-human cytomegalovirus (HCMV) inhibitors.
Laval Chan; T Stefanac; JF Lavallée; H Jin; Jean Bédard; S May; Guy Falardeau
Design and synthesis of new potent human cytomegalovirus (HCMV) inhibitors based on internally hydrogen-bonded 1,6-naphthyridines.
Guy Falardeau; Laval Chan; T Stefanac; S May; H Jin; JF Lavallée
Substituted 1,6-naphthyridines as human cytomegalovirus inhibitors: conformational requirements.

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All Publications

2005: Guy Falardeau; Hugo Lachance; Annie St-Pierre; Constantin G Yannopoulos; Marc Drouin; Jean Bédard; Laval Chan
Design and synthesis of a potent macrocyclic 1,6-naphthyridine anti-human cytomegalovirus (HCMV) inhibitors.
Bioorganic & medicinal chemistry letters 2005;15(6):1693-5.
2001: Laval Chan; T Stefanac; JF Lavallée; H Jin; Jean Bédard; S May; Guy Falardeau
Design and synthesis of new potent human cytomegalovirus (HCMV) inhibitors based on internally hydrogen-bonded 1,6-naphthyridines.
Bioorganic & medicinal chemistry letters 2001;11(2):103-5.
2000: Guy Falardeau; Laval Chan; T Stefanac; S May; H Jin; JF Lavallée
Substituted 1,6-naphthyridines as human cytomegalovirus inhibitors: conformational requirements.
Bioorganic & medicinal chemistry letters 2000;10(24):2769-70.
1999: Laval Chan; H Jin; T Stefanac; JF Lavallée; Guy Falardeau; Wuyi Wang; Jean Bédard; S May; L Yuen
Discovery of 1,6-naphthyridines as a novel class of potent and selective human cytomegalovirus inhibitors.
Journal of medicinal chemistry 1999;42(16):3023-5.
1999: DL Taylor; Parvin Ahmed; P Chambers; AS Tyms; J Bedard; J Duchaine; Guy Falardeau; JF Lavallée; W Brown; RF Rando; Terry Bowlin
Pyrido [1,2a] indole derivatives identified as novel non-nucleoside reverse transcriptase inhibitors of human immunodeficiency virus type 1.
Antiviral chemistry & chemotherapy 1999;10(2):79-86.

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