The therapeutic voyage of pyrazole and its analogs: a review

MF Khan, MM Alam, G Verma, W Akhtar… - European journal of …, 2016 - Elsevier
Pyrazole, a five membered heteroaromatic ring with two nitrogen atoms is of immense
significance. Presence of this nucleus in the pharmacological agents of diverse therapeutic …

Targeting Phenotypically Tolerant Mycobacterium tuberculosis

B Gold, C Nathan - Tuberculosis and the Tubercle Bacillus, 2017 - Wiley Online Library
Two parallel revolutions were born in the golden era of antibiotics (~ 1940 to 1960). One
was a revolution in medicine as physicians went to war with microbes. The second was a …

[HTML][HTML] The genome of the heartworm, Dirofilaria immitis, reveals drug and vaccine targets

C Godel, S Kumar, G Koutsovoulos, P Ludin… - The FASEB …, 2012 - ncbi.nlm.nih.gov
The heartworm Dirofilaria immitis is an important parasite of dogs. Transmitted by
mosquitoes in warmer climatic zones, it is spreading across southern Europe and the …

Oxidative phosphorylation as a target space for tuberculosis: success, caution, and future directions

GM Cook, K Hards, E Dunn, A Heikal… - Tuberculosis and the …, 2017 - Wiley Online Library
The genus Mycobacterium comprises a group of obligately aerobic bacteria that have
adapted to inhabit a wide range of intracellular and extracellular environments …

Structural Basis of Ligand Binding to UDP-Galactopyranose Mutase from Mycobacterium tuberculosis Using Substrate and Tetrafluorinated Substrate Analogues

KE Van Straaten, JRA Kuttiyatveetil… - Journal of the …, 2015 - ACS Publications
UDP-Galactopyranose mutase (UGM) is a flavin-containing enzyme that catalyzes the
reversible conversion of UDP-galactopyranose (UDP-Gal p) to UDP-galactofuranose (UDP …

The search for herbal antibiotics: An in-silico investigation of antibacterial phytochemicals

M Snow Setzer, J Sharifi-Rad, WN Setzer - Antibiotics, 2016 - mdpi.com
Recently, the emergence and spread of pathogenic bacterial resistance to many antibiotics
(multidrug-resistant strains) have been increasing throughout the world. This phenomenon …

Leishmania cell wall as a potent target for antiparasitic drugs. A focus on the glycoconjugates

Y Cabezas, L Legentil, F Robert-Gangneux… - Organic & …, 2015 - pubs.rsc.org
Although leishmaniasis has been studied for over a century, the fight against cutaneous,
mucocutaneous and visceral forms of the disease remains a hot topic. This review refers to …

Biosynthesis of Galactan in Mycobacterium tuberculosis as a Viable TB Drug Target?

Z Konyariková, K Savková, S Kozmon, K Mikušová - Antibiotics, 2020 - mdpi.com
While target-based drug design has proved successful in several therapeutic areas, this
approach has not yet provided compelling outcomes in the field of antibacterial agents. This …

Natural and Synthetic Flavonoids as Potent Mycobacterium tuberculosis UGM Inhibitors

SA Villaume, J Fu, I N'Go, H Liang… - … A European Journal, 2017 - Wiley Online Library
This study reports a novel class of inhibitors of uridine 5′‐diphosphate (UDP)
galactopyranose mutase (UGM) derived from a screening of natural products. This enzyme …

Virtual screening for UDP-galactopyranose mutase ligands identifies a new class of antimycobacterial agents

VA Kincaid, N London, K Wangkanont… - ACS chemical …, 2015 - ACS Publications
Galactofuranose (Gal f) is present in glycans critical for the virulence and viability of several
pathogenic microbes, including Mycobacterium tuberculosis, yet the monosaccharide is …