56247-28-0Relevant academic research and scientific papers
Synthesis and Antibacterial Activity of Novel 3-N-Substituted 1,8-Naphthyridin-2(1H)-ones
Sakram,Kurumanna,Ashok,Rambabu,Ravi,Sathish Kumar
, p. 2534 - 2543 (2019)
Synthesis of novel N-protected and unprotected 3-N-substituted 1,8-naphthyridin-2(1H)-ones with potential inhibiting activity of penicillin-binding protein 6 (PBP6) has been developed. The synthesis is designed around a Buchwald–Hartwig crosscoupling of v
QUINOLIN-2-ONE DERIVATIVES
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Page/Page column 50; 51; 52, (2017/08/07)
Compounds of the formula (I) in which X1, X2, X3, X4, R1, R2, R3, Q and Y have the meanings indicated in Claim 1, are inhibitors of c-Kit kinase, and can be employed for the treatment of cancer.
HCV NS3 PROTEASE INHIBITORS
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Page/Page column 67, (2008/12/05)
The present invention relates to macrocyclic compounds of formula (I) that are useful as inhibitors of the hepatitis C virus (HCV) NS3 protease, their synthesis, and their use for treating or preventing HCV infections.
