Significance and biological importance of pyrimidine in the microbial world

V Sharma, N Chitranshi… - International journal of …, 2014 - Wiley Online Library
Microbes are unique creatures that adapt to varying lifestyles and environment resistance in
extreme or adverse conditions. The genetic architecture of microbe may bear a significant …

Rearrangement of N-Oxyenamines and Related Reactions

AA Tabolin, SL Ioffe - Chemical Reviews, 2014 - ACS Publications
Hydroxylamines and their derivatives have found a wide range of applications in organic
synthesis. 1 In this review we hope to cover the synthetic applications of N …

Structural and biochemical basis for development of influenza virus inhibitors targeting the PA endonuclease

RM DuBois, PJ Slavish, BM Baughman, MK Yun… - PLoS …, 2012 - journals.plos.org
Emerging influenza viruses are a serious threat to human health because of their pandemic
potential. A promising target for the development of novel anti-influenza therapeutics is the …

Targeting Metalloenzymes: The “Achilles' Heel” of Viruses and Parasites

D Moianos, GM Prifti, M Makri, G Zoidis - Pharmaceuticals, 2023 - mdpi.com
Metalloenzymes are central to the regulation of a wide range of essential viral and parasitic
functions, including protein degradation, nucleic acid modification, and many others. Given …

4,5-Dihydroxypyrimidine Carboxamides and N-Alkyl-5-hydroxypyrimidinone Carboxamides Are Potent, Selective HIV Integrase Inhibitors with Good Pharmacokinetic …

V Summa, A Petrocchi, VG Matassa… - Journal of medicinal …, 2006 - ACS Publications
The dihydroxypyrimidine carboxamide 4a was discovered as a potent and selective HIV
integrase strand transfer inhibitor. The optimization of physicochemical properties …

Inhibitors of the hepatitis C virus RNA-dependent RNA polymerase NS5B

MH Powdrill, JA Bernatchez, M Götte - Viruses, 2010 - pmc.ncbi.nlm.nih.gov
More than 20 years after the identification of the hepatitis C virus (HCV) as a novel human
pathogen, the only approved treatment remains a combination of pegylated interferon-α and …

[HTML][HTML] Synthesis and characterization of violurate-based Mn (II) and Cu (II) complexes nano-crystallites as DNA-binders and therapeutics agents against SARS-CoV …

SA Al-Harbi - Journal of Saudi Chemical Society, 2022 - Elsevier
Synthesis and structural characterization of nano crystallites of bis-violurate-based
manganese (II) and copper (II) chelates is the subject of the present study. Analytical data …

RNase H active site inhibitors of human immunodeficiency virus type 1 reverse transcriptase: design, biochemical activity, and structural information

TA Kirschberg, M Balakrishnan… - Journal of medicinal …, 2009 - ACS Publications
Pyrimidinol carboxylic acids were designed as inhibitors of HIV-1 RNase H function. These
molecules can coordinate to two divalent metal ions in the RNase H active site. Inhibition of …

Recent progress in the development of inhibitors of the hepatitis C virus RNA-dependent RNA polymerase

U Koch, F Narjes - Current topics in medicinal chemistry, 2007 - ingentaconnect.com
The global prevalence of hepatitis C virus (HCV) infection and the serious consequences
associated with the chronic state of the disease have become a worldwide health problem. A …

Dihydroxypyrimidine-4-carboxamides as novel potent and selective HIV integrase inhibitors

P Pace, ME Di Francesco, C Gardelli… - Journal of Medicinal …, 2007 - ACS Publications
Human immunodeficiency virus type-1 (HIV-1) integrase, one of the three constitutive viral
enzymes required for replication, is a rational target for chemotherapeutic intervention in the …