314082-69-4Relevant academic research and scientific papers
Highly potent and selective peptide-based inhibitors of the hepatitis C virus serine protease: Towards smaller inhibitors
Llinas-Brunet, Montse,Bailey, Murray,Fazal, Gulrez,Ghiro, Elise,Gorys, Vida,Goulet, Sylvie,Halmos, Ted,Maurice, Roger,Poirier, Martin,Poupart, Marc-Andre,Rancourt, Jean,Thibeault, Diane,Wernic, Dominik,Lamarre, Daniel
, p. 2267 - 2270 (2000)
Structure-activity studies on a hexapeptide N-terminal cleavage product of a dodecamer substrate led to the identification of very potent and highly specific inhibitors of the HCV NS3 protease/NS4A cofactor peptide complex. The largest increase in potency
LINCOMYCIN DERIVATIVE AND ANTIBACTERIAL AGENT CONTAINING THE SAME AS ACTIVE INGREDIENT
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, (2008/12/08)
This invention provides compounds of formula (I) or its pharmacologically acceptable salt or solvate, wherein A represents aryl or a monocyclic or bicyclic heterocyclic group, R1 represents a halide, nitro, substituted C1-6 alkyl, optionally substituted amino, C1-6 alkyloxycarbonyl, optionally substituted aryl, a heterocyclic group, or heterocyclic carbonyl, R2 represents a hydrogen atom or C1-6 alkyl, R3 represents C1-6 alkyl, all of R4, R5, and R6 represent a hydrogen atom, R7 represents C1-6 alkyl, m is 1 or 2, and n is 1. The compounds are novel lincomycin derivatives having a potent activity against resistant pneumococci. The compounds can be used as an antimicrobial agent and are useful for preventing or treating bacterial infectious diseases.
