Minisci reactions: Versatile CH-functionalizations for medicinal chemists
MAJ Duncton - MedChemComm, 2011 - pubs.rsc.org
The addition of a radical to a heteroaromatic base is commonly referred to as a Minsici
reaction. Such reactions constitute a broad-set of selective CH-functionalization processes …
reaction. Such reactions constitute a broad-set of selective CH-functionalization processes …
Antituberculosis drugs: ten years of research
YL Janin - Bioorganic & medicinal chemistry, 2007 - Elsevier
Tuberculosis is today amongst the worldwide health threats. As resistant strains of
Mycobacterium tuberculosis have slowly emerged, treatment failure is too often a fact …
Mycobacterium tuberculosis have slowly emerged, treatment failure is too often a fact …
A Diarylquinoline Drug Active on the ATP Synthase of Mycobacterium tuberculosis
K Andries, P Verhasselt, J Guillemont… - Science, 2005 - science.org
The incidence of tuberculosis has been increasing substantially on a worldwide basis over
the past decade, but no tuberculosis-specific drugs have been discovered in 40 years. We …
the past decade, but no tuberculosis-specific drugs have been discovered in 40 years. We …
High-throughput screening for inhibitors of Mycobacterium tuberculosis H37Rv
S Ananthan, ER Faaleolea, RC Goldman, JV Hobrath… - Tuberculosis, 2009 - Elsevier
There is an urgent need for the discovery and development of new antitubercular agents that
target new biochemical pathways and treat drug resistant forms of the disease. One …
target new biochemical pathways and treat drug resistant forms of the disease. One …
New small-molecule synthetic antimycobacterials
L Ballell, RA Field, K Duncan… - Antimicrobial agents and …, 2005 - Am Soc Microbiol
Drugs for treating tuberculosis (TB) have been available for over half a century, and yet the
incidence of disease worldwide continues to rise year by year. In 2002, the last year for …
incidence of disease worldwide continues to rise year by year. In 2002, the last year for …
Antituberculosis drug research: a critical overview
Beena, DS Rawat - Medicinal research reviews, 2013 - Wiley Online Library
The increasing drug resistance of M ycobacterium tuberculosis to the currently used drugs
and HIV coinfection has caused alarm in the international scientific community …
and HIV coinfection has caused alarm in the international scientific community …
Recent advances in new structural classes of anti-tuberculosis agents
Tuberculosis (TB) is one of the most devastating diseases primarily due to several decades
of neglect and presents a global health threat of escalating proportions. TB is second …
of neglect and presents a global health threat of escalating proportions. TB is second …
Synthesis, anti-tuberculosis activity, and 3D-QSAR study of 4-(adamantan-1-yl)-2-substituted quinolines
Structural optimization of the previously identified 4-(adamantan-1-yl)-2-
quinolinecarbohydrazide (AQCH, MIC= 6.25 μg/mL, 99% inhibition, Mycobacterium …
quinolinecarbohydrazide (AQCH, MIC= 6.25 μg/mL, 99% inhibition, Mycobacterium …
Ring-substituted imidazoles as a new class of anti-tuberculosis agents
We describe in vitro anti-Mycobacterium tuberculosis activities of ring-substituted-1H-
imidazole-4-carboxylic acid derivatives (1–6), and 3-(2-alkyl-1H-imidazol-4-yl)-propionic …
imidazole-4-carboxylic acid derivatives (1–6), and 3-(2-alkyl-1H-imidazol-4-yl)-propionic …
Synthesis and biological evaluation of some new 1, 4-dihydropyridines containing different ester substitute and diethyl carbamoyl group as anti-tubercular agents
Tuberculosis is a leading infectious cause of death worldwide. Because of the concern of the
resistance to most of the commonly used drugs displayed by the considered mycobacteria …
resistance to most of the commonly used drugs displayed by the considered mycobacteria …