Carbohydrate-based therapeutics: a frontier in drug discovery and development

S Mishra, K Upadhaya, KB Mishra, AK Shukla… - Studies in Natural …, 2016 - Elsevier
Carbohydrates, one of the most abundant classes of biomolecules, are the structural
building blocks of genetic materials and vital source of energy. They are integral part of the …

Biochemical and structural characterization of DNA ligases from bacteria and archaea

G Pergolizzi, GK Wagner, RP Bowater - Bioscience Reports, 2016 - portlandpress.com
DNA ligases are enzymes that seal breaks in the backbones of DNA, leading to them being
essential for the survival of all organisms. DNA ligases have been studied from many …

Developments of Corey-Chaykovsky in organic reactions and total synthesis of natural products

MM Heravi, S Asadi, N Nazari… - Current Organic …, 2016 - ingentaconnect.com
The reactions of sulfur ylides with carbonyl, olefin or imine compounds named as the Corey-
Chaykovsky, provide oxiranes, cyclopropane or aziridine, respectively. In this report, we try …

Formal substitution of bromocyclopropanes with nitrogen nucleophiles

JE Banning, J Gentillon, PG Ryabchuk… - The Journal of …, 2013 - ACS Publications
A highly chemo-and diastereoselective protocol toward amino-substituted donor–acceptor
cyclopropanes via the formal nucleophilic displacement in bromocyclopropanes is …

Bile acid amphiphiles with tunable head groups as highly selective antitubercular agents

S Bansal, M Singh, S Kidwai, P Bhargava, A Singh… - …, 2014 - pubs.rsc.org
Tuberculosis faces major challenges for its cure due to (a) long treatment period,(b)
emergence of drug resistance bacteria, and (c) poor patient compliance. Disrupting the …

Formal nucleophilic substitution of bromocyclopropanes with azoles

P Ryabchuk, M Rubina, J Xu, M Rubin - Organic letters, 2012 - ACS Publications
A highly diastereoselective protocol for the formal nucleophilic substitution of 2-
bromocyclopropylcarboxamides with azoles is described. A wide range of azoles, including …

Identification through structure-based methods of a bacterial NAD+-dependent DNA ligase inhibitor that avoids known resistance mutations

K Murphy-Benenato, H Wang, HM McGuire… - Bioorganic & medicinal …, 2014 - Elsevier
In an attempt to identify novel inhibitors of NAD+-dependent DNA ligase (LigA) that are not
affected by a known resistance mutation in the adenosine binding pocket, a detailed …

Homology Modeling of NAD+-Dependent DNA Ligase of the Wolbachia Endosymbiont of Brugia malayi and Its Drug Target Potential Using Dispiro-Cycloalkanones

N Shrivastava, JK Nag, J Pandey… - Antimicrobial Agents …, 2015 - Am Soc Microbiol
Lymphatic filarial nematodes maintain a mutualistic relationship with the endosymbiont
Wolbachia. Depletion of Wolbachia produces profound defects in nematode development …

Structure based identification of first-in-class fragment inhibitors that target the NMN pocket of M. tuberculosis NAD+-dependent DNA ligase A

A Shukla, M Afsar, N Kumar, S Kumar… - Journal of structural …, 2021 - Elsevier
NAD+-dependent DNA ligase (LigA) is the essential replicative ligase in bacteria and differs
from ATP-dependent counterparts like the human DNA ligase I (HligI) in several aspects …

Synthesis and bioevaluation of aryl hydroxamates distinguishing between NAD+ and ATP-dependent DNA ligases

V Kukshal, M Mishra, A Ajay, T Khanam, R Sharma… - …, 2012 - pubs.rsc.org
Identification of compounds distinguishing between NAD+ and ATP-dependent ligases is a
key factor to discover new antimicrobials. Based on virtual screening experiments a series of …