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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-27
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-18
filingDate 1996-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_184bd8e691d2639f7fc0a831460a79d6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f1e17b1392447167591efb19836a5b4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b117052d3e928e989e065a3220364fac
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b9d8a42c42ae4d717783400f1f65cf0f
publicationDate 1997-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2237016-A1
titleOfInvention Azahexane derivatives as substrate isosters of retroviral asparate proteases
abstract The invention relates to compounds of formula (I): wherein R1 and R10 are each independently of the other lower alkoxycarbonyl; either R2, R3 and R4 are each independently of the other C1-C4alkyl and R7, R8 and R9 are each selected from hydrogen and C1-C4alkyl, with not more than 2 of the radicals being hydrogen; or R7, R8 and R9 are each independently of the other C1-C4alkyl and R2, R3 and R4 are each selected from hydrogen and C1-C4alkyl, with 1 or 2 of the radicals being hydrogen; R5 is phenyl or cyclohexyl; and R6 is phenyl or cyanophenyl; or salts thereof; those compounds are inhibitors of retroviral aspartate proteases and are effective, for example, against HIV.
priorityDate 1995-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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