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 …

Structure and inhibition of the drug-resistant S31N mutant of the M2 ion channel of influenza A virus

J Wang, Y Wu, C Ma, G Fiorin, J Wang… - Proceedings of the …, 2013 - National Acad Sciences
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 …

Structural and energetic analysis of drug inhibition of the influenza A M2 proton channel

RX Gu, LA Liu, DQ Wei - Trends in pharmacological sciences, 2013 - cell.com
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 …

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

J Wang, C Ma, J Wang, H Jo, B Canturk… - Journal of medicinal …, 2013 - ACS Publications
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 …

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 …

Role of the viral hemagglutinin in the anti-influenza virus activity of newly synthesized polycyclic amine compounds

E Torres, MD Duque, E Vanderlinden, C Ma, LH Pinto… - Antiviral research, 2013 - Elsevier
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 …

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 …

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 …

[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 …

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 …