2-Aminothiophene scaffolds: Diverse biological and pharmacological attributes in medicinal chemistry

K Bozorov, LF Nie, J Zhao, HA Aisa - European journal of medicinal …, 2017 - Elsevier
Aminothiophenes are important five-membered heterocyclic building blocks in organic
synthesis, and the chemistry of these small molecules is still developing based on the …

A review on enzyme complexes of electron transport chain from Mycobacterium tuberculosis as promising drug targets

P Anand, Y Akhter - International journal of biological macromolecules, 2022 - Elsevier
Energy metabolism is a universal process occurring in all life forms. In Mycobacterium
tuberculosis (Mtb), energy production is carried out in two possible ways, oxidative …

Novel 2‐cyanoacrylamido‐4,5,6,7‐tetrahydrobenzo[b]thiophene derivatives as potent anticancer agents

FM Sroor, MM Aboelenin, KF Mahrous… - Archiv der …, 2020 - Wiley Online Library
Abstract Ethyl 2‐acrylamido‐4, 5, 6, 7‐tetrahydrobenzo [b] thiophene‐3‐carboxylate as well
as its corresponding bis‐derivatives, 5–10, with aliphatic linkers were synthesized, fully …

Synthesis and biological activity of furoxan derivatives against Mycobacterium tuberculosis

GF dos Santos Fernandes, PC de Souza… - European Journal of …, 2016 - Elsevier
Tuberculosis (TB) remains a serious health problem responsible to cause millions of deaths
annually. The scenario becomes alarming when it is evaluated that the number of new drugs …

Alanine dehydrogenase and its applications–A review

UC Dave, RK Kadeppagari - Critical reviews in biotechnology, 2019 - Taylor & Francis
Abstract Alanine dehydrogenase (AlaDH)(EC 1.4. 1.1) is a microbial enzyme that catalyzes
a reversible conversion of L-alanine to pyruvate. Inter-conversion of alanine and pyruvate by …

Drug Discovery for Mycobacterium tuberculosis Using Structure-Based Computer-Aided Drug Design Approach

MA Ejalonibu, SA Ogundare, AA Elrashedy… - International Journal of …, 2021 - mdpi.com
Developing new, more effective antibiotics against resistant Mycobacterium tuberculosis that
inhibit its essential proteins is an appealing strategy for combating the global tuberculosis …

α-Halogenoacetamides: versatile and efficient tools for the synthesis of complex aza-heterocycles

A El Bouakher, A Martel, S Comesse - Organic & Biomolecular …, 2019 - pubs.rsc.org
This review provides an overview of the applications of α-halogenoacetamides in domino
and cycloaddition reactions. α-Halogenoacetamides are versatile building blocks that can …

Design, synthesis, and characterization of N-oxide-containing heterocycles with in vivo sterilizing antitubercular activity

GF dos Santos Fernandes, PC De Souza… - Journal of Medicinal …, 2017 - ACS Publications
Tuberculosis, caused by Mycobacterium tuberculosis (Mtb), is the infectious disease
responsible for the highest number of deaths worldwide. Herein, 22 new N-oxide-containing …

Discovery of a novel dual-target inhibitor of ERK1 and ERK5 that induces regulated cell death to overcome compensatory mechanism in specific tumor types

G Wang, Y Zhao, Y Liu, D Sun, Y Zhen… - Journal of Medicinal …, 2020 - ACS Publications
ERK1 and ERK5 are proposed to have pivotal roles in several types of cancer. Under some
circumstance, ERK5 may provide a common bypass route, which rescues proliferation upon …

Targeting amino acid metabolism of Mycobacterium tuberculosis for developing inhibitors to curtail its survival

SD Yelamanchi, A Surolia - IUBMB life, 2021 - Wiley Online Library
Tuberculosis caused by the bacterium, Mycobacterium tuberculosis (Mtb), continues to
remain one of the most devastating infectious diseases afflicting humans. Although there are …