The lipophilic bullet hits the targets: medicinal chemistry of adamantane derivatives
L Wanka, K Iqbal, PR Schreiner - Chemical reviews, 2013 - ACS Publications
A simple, primary amine bearing a C10H15 alkyl residue was found to display potent anti-
Influenza A properties in 1964. 1 Soon thereafter, antiviral activity of this amine was found …
Influenza A properties in 1964. 1 Soon thereafter, antiviral activity of this amine was found …
Structure and inhibition of the drug-resistant S31N mutant of the M2 ion channel of influenza A virus
The influenza A virus M2 proton channel (A/M2) is the target of the antiviral drugs
amantadine and rimantadine, whose use has been discontinued due to widespread drug …
amantadine and rimantadine, whose use has been discontinued due to widespread drug …
Structural and energetic analysis of drug inhibition of the influenza A M2 proton channel
The type A influenza virus matrix protein 2 (M2) is a highly selective proton channel in the
viral envelope. Because of its crucial role in viral infection and replication, the M2 channel …
viral envelope. Because of its crucial role in viral infection and replication, the M2 channel …
Discovery of novel dual inhibitors of the wild-type and the most prevalent drug-resistant mutant, S31N, of the M2 proton channel from influenza A virus
Anti-influenza drugs, amantadine and rimantadine, targeting the M2 channel from influenza
A virus are no longer effective because of widespread drug resistance. S31N is the …
A virus are no longer effective because of widespread drug resistance. S31N is the …
3-Azatetracyclo[5.2.1.15,8.01,5]undecane Derivatives: From Wild-Type Inhibitors of the M2 Ion Channel of Influenza A Virus to Derivatives with Potent Activity against …
M Rey-Carrizo, E Torres, C Ma… - Journal of medicinal …, 2013 - ACS Publications
We have synthesized and characterized a series of compounds containing the 3-
azatetracyclo [5.2. 1.15, 8.01, 5] undecane scaffold designed as analogues of amantadine …
azatetracyclo [5.2. 1.15, 8.01, 5] undecane scaffold designed as analogues of amantadine …
Role of the viral hemagglutinin in the anti-influenza virus activity of newly synthesized polycyclic amine compounds
We here report on the synthesis of new series of polycyclic amines initially designed as ring-
rearranged analogs of amantadine and featuring pentacyclo, hexacyclo, and octacyclo …
rearranged analogs of amantadine and featuring pentacyclo, hexacyclo, and octacyclo …
Detection of proton movement directly across viral membranes to identify novel influenza virus M2 inhibitors
C Sulli, SSR Banik, J Schilling, A Moser… - Journal of …, 2013 - Am Soc Microbiol
The influenza virus M2 protein is a well-validated yet underexploited proton-selective ion
channel essential for influenza virus infectivity. Because M2 is a toxic viral ion channel …
channel essential for influenza virus infectivity. Because M2 is a toxic viral ion channel …
Design and Development of NS5B Polymerase Non‐nucleoside Inhibitors for the Treatment of Hepatitis C Virus Infection
PL Beaulieu - 2013 - books.rsc.org
Hepatitis C virus (HCV) infects an estimated 170–200 million people worldwide and is
associated with life-threatening liver diseases such as cirrhosis and hepatocellular …
associated with life-threatening liver diseases such as cirrhosis and hepatocellular …
[图书][B] Catalytic cascades creating novel architecture for medicinal chemistry
EEE Elboray - 2013 - etheses.whiterose.ac.uk
The thesis comprises five chapters. Chapter one, the introduction, starts with a brief
discussion of the more famous Pd catalysed reactions and their relevance to Pd as a catalyst …
discussion of the more famous Pd catalysed reactions and their relevance to Pd as a catalyst …
Nouvelles réactions de contraction de cycle: outils pour la construction d'édifices organisés
G Chaubet - 2013 - theses.hal.science
Ces travaux de thèse s' inscrivent dans un projet à long terme concernant le développement
de nouvelles réactions de contraction de cycle originales afin d'accéder à des édifices …
de nouvelles réactions de contraction de cycle originales afin d'accéder à des édifices …