Boron containing compounds as protease inhibitors

R Smoum, A Rubinstein, VM Dembitsky… - Chemical …, 2012 - ACS Publications
Proteases form one of the largest and more important groups of enzymes. They selectively
catalyze the hydrolysis of peptide bonds and can be divided into four major classes …

Polyoxometalate HIV-1 protease inhibitors. A new mode of protease inhibition

DA Judd, JH Nettles, N Nevins, JP Snyder… - Journal of the …, 2001 - ACS Publications
Nb-containing polyoxometalates (POMs) of the Wells− Dawson class inhibit HIV-1 protease
(HIV-1P) by a new mode based on kinetics, binding, and molecular modeling studies …

Regulation of retroviral and SARS-CoV-2 protease dimerization and activity through reversible oxidation

DA Davis, H Bulut, P Shrestha, H Mitsuya, R Yarchoan - Antioxidants, 2022 - mdpi.com
Most viruses encode their own proteases to carry out viral maturation and these often
require dimerization for activity. Studies on human immunodeficiency virus type 1 (HIV-1) …

Convenient method for the preparation of weinreb amides via Pd-catalyzed aminocarbonylation of aryl bromides at atmospheric pressure

JR Martinelli, DMM Freckmann, SL Buchwald - Organic letters, 2006 - ACS Publications
Convenient Method for the Preparation of Weinreb Amides via Pd-Catalyzed Aminocarbonylation
of Aryl Bromides at Atmospheric Pressure | Organic Letters ACS ACS Publications C&EN CAS …

Synthesis and preliminary pharmacological evaluation of some cytisine derivatives

CC Boido, F Sparatore - Il Farmaco, 1999 - Elsevier
Thirty-one N-derivatives of cytisine were prepared in order to modify its pharmacological
profile and to obtain compounds of potential therapeutic interest either at a peripheral or …

[HTML][HTML] L-chicoric acid inhibits human immunodeficiency virus type 1 integration in vivo and is a noncompetitive but reversible inhibitor of HIV-1 integrase in vitro

RA Reinke, DJ Lee, BR McDougall, PJ King, J Victoria… - Virology, 2004 - Elsevier
The human immunodeficiency virus (HIV) integrase (IN) must covalently join the viral cDNA
into a host chromosome for productive HIV infection. l-Chicoric acid (l-CA) enters cells poorly …

Towards a pharmacochemical hypothesis of the prophylaxis of SARS-CoV-2 by psychoactive substances

H Javelot, J Petrignet, F Addiego, J Briet, M Solis… - Medical hypotheses, 2020 - Elsevier
An increasing body of evidence suggests a protective effect of some psychoactive
substances against SARS-CoV-2 (Severe Acute Respiratory Syndrome coronavirus type 2) …

Conjugate addition of amino acid side chains to alkynones and alkynoic acid derivatives

GT Crisp, MJ Millan - Tetrahedron, 1998 - Elsevier
Suitably protected amino acids were used to investigate the Michael addition of the sulfanyl
group of cysteine, the hydroxyl group of serine and the ε-amino group of lysine to a …

Epoxide-containing side chains enhance antiproliferative activity of paullones

X Xie, T Lemcke, R Gussio, DW Zaharevitz… - European journal of …, 2005 - Elsevier
The introduction of side chains bearing epoxide motifs into the molecular scaffold of
kenpaullone and 9-trifluoromethylpaullone led to improved antiproliferative activity of the …

Solution kinetics measurements suggest HIV-1 protease has two binding sites for darunavir and amprenavir

AY Kovalevsky, AK Ghosh, IT Weber - Journal of medicinal …, 2008 - ACS Publications
Darunavir, a potent antiviral drug, showed an unusual second binding site on the HIV-1
protease dimer surface of the V32I drug resistant mutant and normal binding in the active …