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filingDate 1997-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b117052d3e928e989e065a3220364fac
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_184bd8e691d2639f7fc0a831460a79d6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b9d8a42c42ae4d717783400f1f65cf0f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4a85c570ca7410f2617fed73f1e07d20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2c49773506ce123111b88946fe76e7b6
publicationDate 1999-01-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-337398-A3
titleOfInvention Heterocyclic azahexane derivatives, processes for their preparation, pharmaceutical compositions containing them and their use
abstract There are described compounds of formula (I*) wherein R1 is lower alkoxycarbonyl, R2 is secondary or tertiary lower alkyl or lower alkylthio-lower alkyl, R3 is phenyl that is unsubsituted or substituted by one or more lower alkoxy radicals, or C4-C8cycloalkyl, R4 is phenyl or cyclohexyl each substituted in the 4-position by unsaturated heterocyclyl that is bonded by way of a ring carbon atom, has from 5 to 8 ring atoms, contains from 1 to 4 hetero atoms selected from nitrogen, oxygen, sulfur, sulfinyl (-SO-) and sulfonyl (-SO2-) and is unsubstituted or substituted by lower alkyl or by phenyl-lower alkyl, R5, independently of R2, has one of the meanings mentioned for R2, and R6, independently of R1, is lower alkoxycarbonyl, or salts thereof, provided that at least one salt-forming group is present. The compounds are inhibitors of retroviral aspartate protease and can be used, for example, in the treatment of AIDS. They exhibit outstanding pharmacodynamic properties.
priorityDate 1996-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 728.