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Title:
【発明の名称】新規なHIVプロテアーゼ阻害剤
Document Type and Number:
Japanese Patent JPH10505576
Kind Code:
A
Abstract:
Oligopeptide analogs containing sulfonamide, urea or carbamate linkages in the backbone are described. These compounds are useful in the inhibition of HIV protease, the prevention or treatment of infection by HIV and the treatment of AIDS, either as compounds, pharmaceutically acceptable salts, pharmaceutical composition ingredients, whether or not in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating AIDS and methods of preventing or treating infection by HIV are also described.

Inventors:
Rundle Davryu, Hangate
Batka, Joseph Py
Application Number:
JP50254396A
Publication Date:
June 02, 1998
Filing Date:
June 19, 1995
Export Citation:
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Assignee:
Merck End Company, Inc.
International Classes:
C07D295/20; A61K31/165; A61K31/17; A61K31/18; A61K31/27; A61K31/34; A61K31/341; A61K31/38; A61K31/381; A61K31/382; A61K31/41; A61K31/42; A61K31/423; A61K31/44; A61K31/4406; A61K31/4418; A61K31/535; A61K31/5375; A61K31/5377; A61P31/12; A61P43/00; C07C237/22; C07C271/22; C07C271/24; C07C275/10; C07C311/01; C07C311/15; C07C311/19; C07C311/42; C07D213/40; C07D213/56; C07D263/52; C07D295/215; C07D307/14; C07D307/20; C07D333/46; C07D335/06; C07D521/00; (IPC1-7): C07C271/22; C07D521/00; C07D335/06; C07D333/46; C07D307/20; C07D295/20; C07D263/52; C07D213/56; C07D213/40; C07C311/15; C07C311/01; C07C275/10; C07C237/22; A61K31/535; A61K31/44; A61K31/42; A61K31/41; A61K31/38; A61K31/34; A61K31/27; A61K31/18; A61K31/17; A61K31/165
Attorney, Agent or Firm:
Yoshio Kawaguchi (3 outside)