Synthetic approaches and pharmacological activity of 1, 3, 4-oxadiazoles: a review of the literature from 2000–2012

CS De Oliveira, BF Lira, JM Barbosa-Filho… - Molecules, 2012 - mdpi.com
Molecules | Free Full-Text | Synthetic Approaches and Pharmacological Activity of 1,3,4-Oxadiazoles:
A Review of the Literature from 2000–2012 Next Article in Journal Chemical Composition of …

The importance of new companies for drug discovery: origins of a decade of new drugs

R Kneller - Nature reviews Drug discovery, 2010 - nature.com
Understanding the factors that promote drug innovation is important both for improvements
in health care and for the future of organizations engaged in drug discovery research and …

Cytotoxic effect, enzyme inhibition, and in silico studies of some novel N-substituted sulfonyl amides incorporating 1,3,4-oxadiazol structural motif

Ö Güleç, C Türkeş, M Arslan, Y Demir, Y Yeni… - Molecular Diversity, 2022 - Springer
The acetylcholinesterase and carbonic anhydrase inhibitors (AChEIs and h CAIs) remain
key therapeutic agents for many bioactivities such as anti-Alzheimer and antiobesity …

Synopsis of some recent tactical application of bioisosteres in drug design

NA Meanwell - Journal of medicinal chemistry, 2011 - ACS Publications
The concept of isosterism between relatively simple chemical entities was originally
contemplated by James Moir in 1909, a notion further refined by HG Grimm's hydride …

Raltegravir with optimized background therapy for resistant HIV-1 infection

RT Steigbigel, DA Cooper, PN Kumar… - … England Journal of …, 2008 - Mass Medical Soc
Background Raltegravir (MK-0518) is an inhibitor of human immunodeficiency virus type 1
(HIV-1) integrase active against HIV-1 susceptible or resistant to older antiretroviral drugs …

K10 montmorillonite clays as environmentally benign catalysts for organic reactions

BS Kumar, A Dhakshinamoorthy… - Catalysis Science & …, 2014 - pubs.rsc.org
Montmorillonite is one of the most intensively explored catalytic materials in heterogeneous
catalysis due to its low cost and eco-friendliness. Also, it possesses some unique properties …

Chloroquine: modes of action of an undervalued drug

R Thomé, SCP Lopes, FTM Costa, L Verinaud - Immunology letters, 2013 - Elsevier
For more than two decades, chloroquine (CQ) was largely and deliberately used as first
choice drug for malaria treatment. However, worldwide increasing cases of resistant strains …

New class of HIV-1 integrase (IN) inhibitors with a dual mode of action

M Tsiang, GS Jones, A Niedziela-Majka, E Kan… - Journal of Biological …, 2012 - ASBMB
tert-Butoxy-(4-phenyl-quinolin-3-yl)-acetic acids (tBPQA) are a new class of HIV-1 integrase
(IN) inhibitors that are structurally distinct from IN strand transfer inhibitors but analogous to …

Fabs enable single particle cryoEM studies of small proteins

S Wu, A Avila-Sakar, JM Kim, DS Booth, CH Greenberg… - Structure, 2012 - cell.com
In spite of its recent achievements, the technique of single particle electron cryomicroscopy
(cryoEM) has not been widely used to study proteins smaller than 100 kDa, although it is a …

Applications of 2D descriptors in drug design: a DRAGON tale

AM Helguera, RD Combes… - Current topics in …, 2008 - ingentaconnect.com
In order to minimize expensive drug failures, is essential to determine potential activity,
toxicity and ADME problems as early as possible. In view of the large libraries of compounds …