Filovirus Antiviral Activity of Cationic Amphiphilic Drugs Is Associated with Lipophilicity and Ability To Induce Phospholipidosis
出版年份 2020 全文链接
标题
Filovirus Antiviral Activity of Cationic Amphiphilic Drugs Is Associated with Lipophilicity and Ability To Induce Phospholipidosis
作者
关键词
-
出版物
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
Volume 64, Issue 8, Pages -
出版商
American Society for Microbiology
发表日期
2020-06-08
DOI
10.1128/aac.00143-20
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Characterization of the Filovirus-Resistant Cell Line SH-SY5Y Reveals Redundant Role of Cell Surface Entry Factors
- (2019) Francisco Zapatero-Belinchón et al. Viruses-Basel
- Identification of Broad-Spectrum Antiviral Compounds by Targeting Viral Entry
- (2019) Michela Mazzon et al. Viruses-Basel
- A central hydrophobic E1 region controls the pH range of hepatitis C virus membrane fusion and susceptibility to fusion inhibitors
- (2019) Dominic H. Banda et al. JOURNAL OF HEPATOLOGY
- Target Identification and Mode of Action of Four Chemically Divergent Drugs against Ebolavirus Infection
- (2018) Jingshan Ren et al. JOURNAL OF MEDICINAL CHEMISTRY
- PubChem 2019 update: improved access to chemical data
- (2018) Sunghwan Kim et al. NUCLEIC ACIDS RESEARCH
- DrugBank 5.0: a major update to the DrugBank database for 2018
- (2017) David S Wishart et al. NUCLEIC ACIDS RESEARCH
- The Ebola outbreak, 2013–2016: old lessons for new epidemics
- (2017) Cordelia E. M. Coltart et al. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES
- Toremifene interacts with and destabilizes the Ebola virus glycoprotein
- (2016) Yuguang Zhao et al. NATURE
- Cationic amphiphilic drugs enhance entry of lentiviral particles pseudotyped with rabies virus glycoprotein into non-neuronal cells
- (2015) Anneke Klintworth et al. ANTIVIRAL RESEARCH
- Flunarizine prevents hepatitis C virus membrane fusion in a genotype-dependent manner by targeting the potential fusion peptide within E1
- (2015) Paula M. Perin et al. HEPATOLOGY
- Ebolavirus Glycoprotein Directs Fusion through NPC1 + Endolysosomes
- (2015) James A. Simmons et al. JOURNAL OF VIROLOGY
- Antiviral drug discovery: broad-spectrum drugs from nature
- (2015) J. P. Martinez et al. NATURAL PRODUCT REPORTS
- Combating emerging viral threats
- (2015) E. Bekerman et al. SCIENCE
- Repurposing of the antihistamine chlorcyclizine and related compounds for treatment of hepatitis C virus infection
- (2015) Shanshan He et al. Science Translational Medicine
- A screen of approved drugs and molecular probes identifies therapeutics with anti–Ebola virus activity
- (2015) Lisa M. Johansen et al. Science Translational Medicine
- Amiodarone and metabolite MDEA inhibit Ebola virus infection by interfering with the viral entry process
- (2015) Cristiano Salata et al. Pathogens and Disease
- Evaluation of Ebola Virus Inhibitors for Drug Repurposing
- (2015) Peter B. Madrid et al. ACS Infectious Diseases
- Ebola Virus and Severe Acute Respiratory Syndrome Coronavirus Display Late Cell Entry Kinetics: Evidence that Transport to NPC1+Endolysosomes Is a Rate-Defining Step
- (2015) Rebecca M. Mingo et al. JOURNAL OF VIROLOGY
- The clinically approved drugs amiodarone, dronedarone and verapamil inhibit filovirus cell entry
- (2014) Gerrit Gehring et al. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
- Lassa Fever in Post-Conflict Sierra Leone
- (2014) Jeffrey G. Shaffer et al. PLoS Neglected Tropical Diseases
- Amiodarone inhibits the entry and assembly steps of hepatitis C virus life cycle
- (2013) Yuan-Lung Cheng et al. CLINICAL SCIENCE
- Chemically Advanced Template Search (CATS) for Scaffold-Hopping and Prospective Target Prediction for ‘Orphan’ Molecules
- (2013) Michael Reutlinger et al. Molecular Informatics
- Multiple Cationic Amphiphiles Induce a Niemann-Pick C Phenotype and Inhibit Ebola Virus Entry and Infection
- (2013) Charles J. Shoemaker et al. PLoS One
- FDA-Approved Selective Estrogen Receptor Modulators Inhibit Ebola Virus Infection
- (2013) L. M. Johansen et al. Science Translational Medicine
- Impact of Intra- and Interspecies Variation of Occludin on Its Function as Coreceptor for Authentic Hepatitis C Virus Particles
- (2011) S. Ciesek et al. JOURNAL OF VIROLOGY
- Small molecule inhibitors reveal Niemann–Pick C1 is essential for Ebola virus infection
- (2011) Marceline Côté et al. NATURE
- Chemical combinations elucidate pathway interactions and regulation relevant to Hepatitis C replication
- (2010) Christopher M Owens et al. Molecular Systems Biology
- A cell protection screen reveals potent inhibitors of multiple stages of the hepatitis C virus life cycle
- (2010) Karuppiah Chockalingam et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Intracellular sequestration of amiodarone: role of vacuolar ATPase and macroautophagic transition of the resulting vacuolar cytopathology
- (2009) G Morissette et al. BRITISH JOURNAL OF PHARMACOLOGY
- Production, concentration and titration of pseudotyped HIV-1-based lentiviral vectors
- (2009) Robert H Kutner et al. Nature Protocols
- Unbiased probing of the entire hepatitis C virus life cycle identifies clinical compounds that target multiple aspects of the infection
- (2009) P. Gastaminza et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Amiodarone Alters Late Endosomes and Inhibits SARS Coronavirus Infection at a Post-Endosomal Level
- (2008) Konrad Stadler et al. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY
- Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium
- (2008) Emyr Lloyd-Evans et al. NATURE MEDICINE
- A 96-well flow cytometric screening assay for detecting in vitro phospholipidosis-induction in the drug discovery phase
- (2008) Mesens Natalie et al. TOXICOLOGY IN VITRO
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started