18 articles for R De Francesco
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
Discovery of (7R)-14-cyclohexyl-7-{[2-(dimethylamino)ethyl](methyl) amino}-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylic acid (MK-3281), a potent and orally bioavailable finger-loop inhibitor of the hepatitis C virus NS5B polymerase.

P. Angeletti S.P.A. (Merck Research Laboratories)
Unraveling the hidden catalytic activity of vertebrate class IIa histone deacetylases.

Istituto Di Ricerche Di Biologia Molecolare
A series of novel, potent, and selective histone deacetylase inhibitors.

Irbm/Merck Research Laboratories
Mechanism of hepatitis C virus RNA polymerase inhibition with dihydroxypyrimidines.

Mcgill University
Hepatitis C virus NS5A is a direct substrate of casein kinase I-alpha, a cellular kinase identified by inhibitor affinity chromatography using specific NS5A hyperphosphorylation inhibitors.

Istituto Di Ricerche Di Biologia Molecolare &Quot;P. Angeletti
A structure-guided approach to an orthogonal estrogen-receptor-based gene switch activated by ligands suitable for in vivo studies.

Irbm (Merck Research Laboratories Rome)
2-(2-Thienyl)-5,6-dihydroxy-4-carboxypyrimidines as inhibitors of the hepatitis C virus NS5B polymerase: discovery, SAR, modeling, and mutagenesis.

P. Angeletti S.P.A. (Merck Research Laboratories)
Potent inhibitors of subgenomic hepatitis C virus RNA replication through optimization of indole-N-acetamide allosteric inhibitors of the viral NS5B polymerase.

Irbm (Merck Research Laboratories Rome)
Development and preliminary optimization of indole-N-acetamide inhibitors of hepatitis C virus NS5B polymerase.

Irbm (Merck Research Laboratories Rome)
Discovery and antiviral profile of new sulfamoylbenzamide derivatives as HBV capsid assembly modulators.

Promidis
HCV NS5b RNA-dependent RNA polymerase inhibitors: from alpha,gamma-diketoacids to 4,5-dihydroxypyrimidine- or 3-methyl-5-hydroxypyrimidinonecarboxylic acids. Design and synthesis.

Italy. Vinc
The monoethyl ester of meconic acid is an active site inhibitor of HCV NS5B RNA-dependent RNA polymerase.

Mrl Rome
Discovery of alpha,gamma-diketo acids as potent selective and reversible inhibitors of hepatitis C virus NS5b RNA-dependent RNA polymerase.

Italy. Vinc
Phenethyl amides as novel noncovalent inhibitors of hepatitis C virus NS3/4A protease: discovery, initial SAR, and molecular modeling.

Mrl Rome
A designed P1 cysteine mimetic for covalent and non-covalent inhibitors of HCV NS3 protease.

Irbm, Mrl Rome
Substituted triazoles useful as Axl inhibitors

Rigel Pharmaceuticals
1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazoles: identification of a potent aurora kinase inhibitor with a favorable antitumor kinase inhibition profile.

Nerviano Medical Sciences
Potent and selective nonpeptide inhibitors of caspases 3 and 7.

Glaxosmithkline