Organic carbamates in drug design and medicinal chemistry

AK Ghosh, M Brindisi - Journal of medicinal chemistry, 2015 - ACS Publications
The carbamate group is a key structural motif in many approved drugs and prodrugs. There
is an increasing use of carbamates in medicinal chemistry and many derivatives are …

Recent Progress in the Development of HIV-1 Protease Inhibitors for the Treatment of HIV/AIDS

AK Ghosh, HL Osswald, G Prato - Journal of medicinal chemistry, 2016 - ACS Publications
HIV-1 protease inhibitors continue to play an important role in the treatment of HIV/AIDS,
transforming this deadly ailment into a more manageable chronic infection. Over the years …

A survey of the structures of US FDA approved combination drugs

P Das, MD Delost, MH Qureshi, DT Smith… - Journal of medicinal …, 2018 - ACS Publications
Combination drugs are an important class of US FDA approved pharmaceuticals. These
drugs have been on a continuous growth trajectory since the first combination drugs were …

Molecular recognition in chemical and biological systems

E Persch, O Dumele, F Diederich - … Chemie International Edition, 2015 - Wiley Online Library
Abstract Structure‐based ligand design in medicinal chemistry and crop protection relies on
the identification and quantification of weak noncovalent interactions and understanding the …

Develo** β‐secretase inhibitors for treatment of Alzheimer's disease

AK Ghosh, M Brindisi, J Tang - Journal of neurochemistry, 2012 - Wiley Online Library
J. Neurochem.(2012) 120 (Suppl. 1), 71–83. Abstract β‐Secretase (memapsin 2; BACE‐1) is
the first protease in the processing of amyloid precursor protein leading to the production of …

[HTML][HTML] BACE1 function and inhibition: implications of intervention in the amyloid pathway of Alzheimer's disease pathology

G Koelsch - Molecules, 2017 - mdpi.com
Alzheimer's disease (AD) is a fatal progressive neurodegenerative disorder characterized by
increasing loss in memory, cognition, and function of daily living. Among the many …

The interaction of Naphthol Yellow S (NYS) with pepsin: Insights from spectroscopic to molecular dynamics studies

F Hashemi-Shahraki, B Shareghi… - International Journal of …, 2020 - Elsevier
Abstract The effects of Naphthol Yellow S (NYS) on the structure and activity of pepsin were
carried out using ultraviolet–visible (UV–Vis) spectroscopy, intrinsic fluorescence …

Microbial aspartic proteases: current and potential applications in industry

LW Theron, B Divol - Applied microbiology and biotechnology, 2014 - Springer
Aspartic proteases are a relatively small group of proteolytic enzymes that are active in
acidic environments and are found across all forms of life. Certain microorganisms secrete …

Enhancing protein backbone binding—a fruitful concept for combating drug‐resistant HIV

AK Ghosh, DD Anderson, IT Weber… - Angewandte Chemie …, 2012 - Wiley Online Library
The evolution of drug resistance is one of the most fundamental problems in medicine. In
HIV/AIDS, the rapid emergence of drug‐resistant HIV‐1 variants is a major obstacle to …

Design and development of highly potent HIV-1 protease inhibitors with a crown-like oxotricyclic core as the P2-ligand to combat multidrug-resistant HIV variants

AK Ghosh, KV Rao, PR Nyalapatla… - Journal of medicinal …, 2017 - ACS Publications
Design, synthesis, and evaluation of a new class of exceptionally potent HIV-1 protease
inhibitors are reported. Inhibitor 5 displayed superior antiviral activity and drug-resistance …