Repurposing of kinase inhibitors for treatment of COVID-19

E Weisberg, A Parent, PL Yang, M Sattler, Q Liu… - Pharmaceutical …, 2020 - Springer
The outbreak of COVID-19, the pandemic disease caused by the severe acute respiratory
syndrome coronavirus 2 (SARS-CoV-2), has spurred an intense search for treatments by the …

Chemical characteristics, synthetic methods, and biological potential of quinazoline and quinazolinone derivatives

M Asif - International journal of medicinal chemistry, 2014 - Wiley Online Library
The heterocyclic fused rings quinazoline and quinazolinone have drawn a huge
consideration owing to their expanded applications in the field of pharmaceutical chemistry …

Preparing for the next viral threat with broad-spectrum antivirals

M Karim, CW Lo, S Einav - The Journal of Clinical …, 2023 - Am Soc Clin Investig
There is a large global unmet need for the development of countermeasures to combat
hundreds of viruses known to cause human disease and for the establishment of a …

Quinazoline-based VEGFR-2 inhibitors as potential anti-angiogenic agents: A contemporary perspective of SAR and molecular docking studies

M Moradi, A Mousavi, Z Emamgholipour… - European Journal of …, 2023 - Elsevier
Angiogenesis, the formation of new blood vessels from the existing vasculature, is pivotal in
the migration, growth, and differentiation of endothelial cells in normal physiological …

Accessing polysubstituted quinazolines via nickel catalyzed acceptorless dehydrogenative coupling

S Parua, R Sikari, S Sinha, G Chakraborty… - The Journal of …, 2018 - ACS Publications
Two environmentally benign methods for the synthesis of quinazolines via acceptorless
dehydrogenative coupling of 2-aminobenzylamine with benzyl alcohol (Path A) and 2 …

Synthesis, biological evaluation and molecular docking of novel series of spiro [(2H, 3H) quinazoline-2, 1′-cyclohexan]-4 (1H)-one derivatives as anti-inflammatory …

KM Amin, MM Kamel, MM Anwar, M Khedr… - European Journal of …, 2010 - Elsevier
Three series of Spiro [(2H, 3H) quinazoline-2, 1′-cyclohexan]-4 (1H)-one derivatives have
been synthesized. Some of the novel quinazolinone derivatives IIe, VIIIc, XIc, XIIb, XIIc, XVIb …

Viral journeys on the intracellular highways

M Robinson, S Schor, R Barouch-Bentov… - Cellular and Molecular …, 2018 - Springer
Viruses are obligate intracellular pathogens that are dependent on cellular machineries for
their replication. Recent technological breakthroughs have facilitated reliable identification …

Function of human cytomegalovirus UL97 kinase in viral infection and its inhibition by maribavir

MN Prichard - Reviews in medical virology, 2009 - Wiley Online Library
The serine/threonine kinase expressed by human cytomegalovirus from gene UL97
phosphorylates the antiviral drug ganciclovir, but its biological function is the …

Repurposing of kinase inhibitors as broad-spectrum antiviral drugs

S Schor, S Einav - DNA and cell biology, 2018 - liebertpub.com
The high cost of drug development and the narrow spectrum of coverage typically provided
by direct-acting antivirals limit the scalability of this antiviral approach. This review …

In Vitro Evaluation of the Activities of the Novel Anticytomegalovirus Compound AIC246 (Letermovir) against Herpesviruses and Other Human Pathogenic Viruses

M Marschall, T Stamminger, A Urban… - Antimicrobial agents …, 2012 - Am Soc Microbiol
ABSTRACT AIC246 (letermovir) is a potent anticytomegalovirus drug in clinical
development. Here, we report a consistent antiviral efficacy of AIC246 against human …