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filingDate 1999-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b1092cdf08189f9e65aebedc08b62937
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publicationDate 2000-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1008592-A3
titleOfInvention Cyclic amide derivatives which inhibit cathepsin K
abstract Alcohol derivatives represented by the general formula (IV); nwherein: R 1 represents a substituted C 1 -C 12 alkyl group; a substituted C 2 -C 6 alkenyl group; a substituted amino group; a substituted C 1 -C 6 alkoxy group; a substituted C 1 -C 6 alkylthio group; a substituted carbamoyl group; a substituted sulfonamide group; or a substituted amide group; the ring A represents a saturated cyclic alkyl group with 5 to 7 carbon atoms; R 2 represents a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aromatic hydrocarbon group or a substituted or unsubstituted heterocyclic group; R 3 represents a hydrogen atom, a group represented by the general formula R 4 O- ; or a group represented by the general formula R 5 (R 6 )N-wherein R 4 represents a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aromatic hydrocarbon group or a substituted or unsubstituted heterocyclic group; R 5 and R 6 may be the same or different and each represents a hydrogen atom, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aromatic hydrocarbon group or a substituted or unsubstituted heterocyclic group, The cyclic carboxylic acid derivatives of formula (IV) are useful for the synthesis of cyclic amide derivatives useful as cathepsin K inhibitors.
priorityDate 1998-11-12-04:00^^<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: 738.