Title
Design of HIV-1 protease inhibitors active on multidrug-resistant virus
UMMS Affiliation
Department of Biochemistry and Molecular Pharmacology
Publication Date
2005-03-18
Document Type
Article
Subjects
Animals; Benzoxazoles; Binding Sites; Calorimetry; Cell Line; Crystallography, X-Ray; Dogs; *Drug Resistance, Multiple, Viral; Drug Stability; HIV Protease Inhibitors; HIV-1; Humans; Microsomes, Liver; Models, Molecular; Rats; Rats, Wistar; Sulfonamides; Thermodynamics; Thiazoles
Disciplines
Biochemistry, Biophysics, and Structural Biology | Pharmacology, Toxicology and Environmental Health
Abstract
On the basis of structural data gathered during our ongoing HIV-1 protease inhibitors program, from which our clinical candidate TMC114 9 was selected, we have discovered new series of fused heteroaromatic sulfonamides. The further extension into the P2' region was aimed at identifying new classes of compounds with an improved broad spectrum activity and acceptable pharmacokinetic properties. Several of these compounds display an exceptional broad spectrum activity against a panel of highly cross-resistant mutants. Certain members of these series exhibit favorable pharmacokinetic profiles in rat and dog. Crystal structures and molecular modeling were used to rationalize the broad spectrum profile resulting from the extension into the P2' pocket of the HIV-1 protease.
DOI of Published Version
10.1021/jm049454n
Source
J Med Chem. 2005 Mar 24;48(6):1965-73. Link to article on publisher's site
Journal/Book/Conference Title
Journal of medicinal chemistry
Related Resources
PubMed ID
15771440
Repository Citation
Surleraux DL, De Kock HA, Verschueren WG, Pille GM, Maes LJ, Peeters A, Vendeville S, De Meyer S, Azijn H, Pauwels R, de Bethune M, King NM, Prabu-Jeyabalan M, Schiffer CA, Wigerinck PB. (2005). Design of HIV-1 protease inhibitors active on multidrug-resistant virus. Biochemistry and Molecular Pharmacology Publications. https://doi.org/10.1021/jm049454n. Retrieved from https://escholarship.umassmed.edu/bmp_pp/79