S. May

发表

A high throughput colorimetric cell proliferation assay for the identification of human cytomegalovirus inhibitors.

J. Bédard, L. Yuen, D Barbeau, 1999, Antiviral research.

Discovery of 1,6-naphthyridines as a novel class of potent and selective human cytomegalovirus inhibitors.

L. Chan, J. Bédard, H. Jin, 1999, Journal of medicinal chemistry.

Substituted 1,6-naphthyridines as human cytomegalovirus inhibitors: conformational requirements.

L. Chan, H. Jin, T. Stefanac, 2000, Bioorganic & Medicinal Chemistry Letters.

Design and evaluation of dihydroisoquinolines as potent and orally bioavailable human cytomegalovirus inhibitors.

L. Chan, N. Turcotte, J. Bédard, 2000, Bioorganic & medicinal chemistry letters.

Antiviral Properties of a Series of 1,6-Naphthyridine and 7,8-Dihydroisoquinoline Derivatives Exhibiting Potent Activity against Human Cytomegalovirus

L. Chan, L. L'Heureux, J. Bédard, 2000, Antimicrobial Agents and Chemotherapy.

Isoquinoline-6-carboxamides as potent and selective anti-human cytomegalovirus (HCMV) inhibitors.

L. Chan, J. Bédard, H. Jin, 1999, Bioorganic & medicinal chemistry letters.

Comparative Study of the Anti-Human Cytomegalovirus Activities and Toxicities of a Tetrahydrofuran Phosphonate Analogue of Guanosine and Cidofovir

L. Chan, J. Bédard, R. Sidwell, 1999, Antimicrobial Agents and Chemotherapy.

939 PRECLINICAL PHARMACOKINETIC AND ADME CHARACTERIZATION OF VCH-222, A NOVEL NON-NUCLEOSIDE HCV NS5B POLYMERASE INHIBITOR

L. Ste-Marie, N. Chauret, S. May, 2009 .

Design and synthesis of new potent human cytomegalovirus (HCMV) inhibitors based on internally hydrogen-bonded 1,6-naphthyridines.

L. Chan, J. Bédard, H. Jin, 2001, Bioorganic & medicinal chemistry letters.

In vitro Cross-resistance Studies of Five Different Classes of Integrase Inhibitors in Recombinant HIV-1 C

S. May, T. Miletti, †. Ren, 2022 .