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filingDate 2005-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_83d671f32462befd691779ec60ec7c68
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publicationDate 2006-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2006028239-A1
titleOfInvention Carbamoyl-substituted spiro derivative
abstract A compound represented by, e.g., the formula (I): [Chemical formula 1] (I) [wherein X, Y, Z, and W each independently represents optionally substituted methine; A, B, and D each independently represents -C(O)-, etc.; Q represents methine or nitrogen; and R represents a group optionally substituted by lower alkyl, etc. and represented by the formula (II-1): (II-1) (wherein R6 represents lower alkyl, etc.; and R7 and R8 each independently represents lower alkyl, etc.)] or a pharmaceutically acceptable salt of the compound. The compound and salt have antagonistic activity against a histamine H3 receptor or inverse agonistic activity against a histamine H3 receptor. They are useful in the prevention or treatment of metabolic diseases, circulatory diseases, or neurotic diseases.
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priorityDate 2004-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456050265
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419589421
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9968
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11182
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419554419
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24942599
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421227772
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419481582
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID25290
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID8629308
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ86HL5
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID461892
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ5U780
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ5GKZ7
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Total number of triples: 1346.