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filingDate 2001-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a8287e8b2a3e922d7592206f86d35706
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b2dc4d3f6a045f5c056cc948d02aa719
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ece51826ffef7fdcaf94a82d3a2f778f
publicationDate 2009-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2418794-C
titleOfInvention Calcium receptor antagonists
abstract A compound of the formula [I] (see formula I) wherein R2 is optionally substituted aryl group or optionally substituted heteroaryl group; R2 is optionally substituted C1-6 alkyl group, C3-7 cycloalkyl group and the like; R3 is hydrogen atom, C1-6 alkyl group, hydroxyl group and the like; R4 is hydrogen atom, C1-6 alkyl group and the like; R5 and R6 are each C1-6 alkyl group and the like; R7 is optionally substituted aryl group or optionally substituted heteroaryl group; X1, X2 and X3 are each C1-6 alkylene group and the like; and X4 and X5 are each a single bond, methylene group and the like, a salt thereof, a solvate thereof or a prodrug thereof, and a pharmaceutical composition containing the compound, particularly a calcium receptor antagonist and a therapeutic agent for osteoporosis, are provided. The compound of the present invention is useful as a therapeutic drug of diseases accompanied by abnormal calcium homeostasis, or osteoporosis, hypoparathyreosis, osteosarcoma, periodontal disease, bone fracture, steoarthrosis, chronic rheumatoid arthritis, Paget's disease, humoral hypercalcemia, autosomal dominant hypocalcemia and the like. In addition, an intermediate for the compound is provided.
priorityDate 2000-08-11-04:00^^<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: 410.