Identification of small-molecule inhibitors of Zika virus infection and induced neural cell death via a drug repurposing screen
In response to the current global health emergency posed by the Zika virus (ZIKV) outbreak
and its link to microcephaly and other neurological conditions, we performed a drug …
and its link to microcephaly and other neurological conditions, we performed a drug …
Identification of 53 compounds that block Ebola virus-like particle entry via a repurposing screen of approved drugs
J Kouznetsova, W Sun… - Emerging microbes & …, 2014 - Taylor & Francis
In light of the current outbreak of Ebola virus disease, there is an urgent need to develop
effective therapeutics to treat Ebola infection, and drug repurposing screening is a potentially …
effective therapeutics to treat Ebola infection, and drug repurposing screening is a potentially …
[HTML][HTML] Elabela-apelin receptor signaling pathway is functional in mammalian systems
Z Wang, D Yu, M Wang, Q Wang, J Kouznetsova… - Scientific reports, 2015 - nature.com
Elabela (ELA) or Toddler is a recently discovered hormone which is required for normal
development of heart and vasculature through activation of apelin receptor (APJ), a G protein-…
development of heart and vasculature through activation of apelin receptor (APJ), a G protein-…
Discovery and optimization of potent, cell-active pyrazole-based inhibitors of lactate dehydrogenase (LDH)
We report the discovery and medicinal chemistry optimization of a novel series of pyrazole-based
inhibitors of human lactate dehydrogenase (LDH). Utilization of a quantitative high-…
inhibitors of human lactate dehydrogenase (LDH). Utilization of a quantitative high-…
[HTML][HTML] Synergistic drug combination effectively blocks Ebola virus infection
W Sun, S He, C Martínez-Romero, J Kouznetsova… - Antiviral research, 2017 - Elsevier
Although a group of FDA-approved drugs were previously identified with activity against
Ebola virus (EBOV), most of them are not clinically useful because their human blood …
Ebola virus (EBOV), most of them are not clinically useful because their human blood …
Large-scale screening and identification of novel Ebola virus and Marburg virus entry inhibitors
M Anantpadma, J Kouznetsova, H Wang… - Antimicrobial agents …, 2016 - Am Soc Microbiol
Filoviruses are highly infectious, and no FDA-approved drug therapy for filovirus infection is
available. Most work to find a treatment has involved only a few strains of Ebola virus and …
available. Most work to find a treatment has involved only a few strains of Ebola virus and …
A novel quantitative high-throughput screen identifies drugs that both activate SUMO conjugation via the inhibition of microRNAs 182 and 183 and facilitate …
…, D Maric, G Volpe, J Kouznetsova… - Journal of Cerebral …, 2016 - journals.sagepub.com
The conjugation/de-conjugation of Small Ubiquitin-like Modifier (SUMO) has been shown to
be associated with a diverse set of physiologic/pathologic conditions. The clinical …
be associated with a diverse set of physiologic/pathologic conditions. The clinical …
[HTML][HTML] Quantitative high-throughput screening identifies cytoprotective molecules that enhance SUMO conjugation via the inhibition of SUMO-specific protease …
…, YJ Lee, FA Gessler, A Yasgar, J Kouznetsova… - The FASEB …, 2018 - ncbi.nlm.nih.gov
The development of novel neuroprotective treatments for acute stroke has been fraught with
failures, which supports the view of ischemic brain damage as a highly complex …
failures, which supports the view of ischemic brain damage as a highly complex …
Small molecule, NSC95397, inhibits the CtBP1-protein partner interaction and CtBP1-mediated transcriptional repression
MA Blevins, J Kouznetsova… - Journal of …, 2015 - journals.sagepub.com
Carboxyl-terminal binding protein (CtBP) is a transcriptional corepressor that suppresses
multiple proapoptotic and epithelial genes. CtBP is overexpressed in many human cancers, …
multiple proapoptotic and epithelial genes. CtBP is overexpressed in many human cancers, …
Structure–activity relationship studies and biological characterization of human NAD+-dependent 15-hydroxyprostaglandin dehydrogenase inhibitors
The structure–activity relationship (SAR) study of two chemotypes identified as inhibitors of
the human NAD + -dependent 15-hydroxyprostaglandin dehydrogenase (HPGD, 15-PGDH) …
the human NAD + -dependent 15-hydroxyprostaglandin dehydrogenase (HPGD, 15-PGDH) …