http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2008176869-A1

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filingDate 2008-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_30aade65d9ef53e62e1869241687470b
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publicationDate 2008-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2008176869-A1
titleOfInvention Tetrahydro-4H-pyrido[1,2-a] pyrimidines useful as HIV integrase inhibitors
abstract Tetrahydro-4H-pyrido[1,2-a]pyrimidines and related compounds of Formula A: n n n n n n n n n n are described as inhibitors of HIV integrase and inhibitors of HIV replication, wherein n is an integer equal to zero, 1, 2 or 3, and R 1 , R 3 , R 4 , R 12 , R 14 , R 16 , R 30 , R 32 , R 34 and R 36 are defined herein. These compounds are useful in the prevention and treatment of infection by HIV and in the prevention, delay in the onset, and treatment of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8513234-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9649311-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8357798-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2008118559-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2010087419-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10772888-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7754731-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8771733-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2010249410-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006122205-A1
priorityDate 2002-12-27-04:00^^<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: 1442.