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filingDate 2002-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_048fd4e3f1d602cafd75520f695be16e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0f468d5aa64cf67952af46ad769f1516
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_28955791413c21270b580ebc08143cf2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_27a04a8ac34b97a4e202f15bcc4a290c
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4feac6eb020cbfce88aa60c8899fde29
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7dacfd78beb75b8005baf765f1c1b6b2
publicationDate 2003-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2003048880-A
titleOfInvention Cyclic amine compounds, their production and use
abstract (57) [Summary] (Modified) [Problem] To provide a compound that exhibits excellent CCR5 antagonism and is useful as a prophylactic / therapeutic agent for HIV infection of human peripheral blood mononuclear cells, particularly AIDS. SOLUTION: Equation 1, (In the formula, R 1 and R 2 represent a hydrogen atom, a hydrocarbon group, a non-aromatic heterocyclic ring, or R 1 and R 2 may be bonded to form a heterocyclic ring with a nitrogen atom; N or N + -R 5 • Y − (R 5 represents a hydrocarbon group, Y − represents a counter anion), R 3 represents a cyclic hydrocarbon group or a heterocyclic ring, n represents 0 or 1, R 4 represents a hydrogen atom, a hydrocarbon Group, A heterocyclic ring, an alkoxy group, an aryloxy group, or an amino group; E represents a divalent chain hydrocarbon group other than an oxo group; G 1 is a bond, CO or SO 2 , G 2 is CO, SO 2 , NHCO, CONH or OCO, J is a methine or nitrogen atom, Q and R are each a divalent C 1-3 Each chain hydrocarbon is shown. Or a salt thereof.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008525416-A
priorityDate 1999-10-01-04:00^^<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: 1728.