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filingDate 1992-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1b83ea6136f21d9843c3b60f8e5ee87
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publicationDate 1993-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0526009-A1
titleOfInvention Inhibitors of hiv protease useful for the treatment of aids
abstract A pharmaceutical compund having the Formula:n n where: n   R is C₅-C₇ cycloalkyl, heterocycle, aryl or unsaturated heterocycle; n   X is a bond, (-CH₂) q -, -O-(-CH₂-) q -, -(-CH₂-) q -O-or -N(R⁵)(CH₂-) m -; n      n is 0, 1, or 2; n      q is 1, 2, 3 or 4; n   R¹ is aryl or C₅-C₇ cycloalkyl; n   R² is an amino acid side chain, unsaturated heterocycle, unsaturated heterocycle(C₁-C₄ alkanediyl), C₁-C₄ alkylaminocarbonyl(C₁-C₄ alkanediyl), or a group having the structure -CH₂-C(O)-NR⁴-X-R or -CH₂-R; n   Y is an aryl or unsaturated heterocycle; n   R³ is a group having the structure: nn 1) -C(O)-NR⁴R⁴ 2)n 3)n 4)n 5)n 6)n n where: n      1 is 3, 4 or 5; n      m at each occurrence is independently 0, 1, 2, or 3; n      p is 4 or 5; n   R⁴ at each occurrence is independently hydrogen, C₁-C₆ alkyl, or hydroxy(C₁-C₄)alkanediyl; n   R⁵ and R⁶ are independently selected from hydrogen, hydroxy, C₁-C₆ alkyl, C₁-C₆ alkoxy, amino, C₁-C₄alkylamino, hydroxy (C₁-C₄) alkanediyl, carboxy, (C₁-C₄alkoxy)carbonyl, aminocarbonyl, C₁-C₄ alkylaminocarbonyl, aryl, heterocycle or unsaturated heterocycle; nor a pharmaceutically acceptable salt or solvate thereof.
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Total number of triples: 564.