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filingDate 2001-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_efdb01626d549233d2cf02746855ecb2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_72b6be798b77c5b0a088f7366cee3cf9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_11abb8d7cb501efd5a074c6300ce90c1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_906b5629110f343558e61c1aed1afc49
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_05f2f4477e97f3d31e21db6856ae219e
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_18c7c51cf30efecc349cb45f965f3e52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_516d908db3ebc1f25084b3f8168db882
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publicationDate 2002-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2425097-A1
titleOfInvention Benzamide compounds as apo b secretion inhibitors
abstract The present invention relates to compounds of the formula (I) wherein R1 and R2 are each independently lower alkyl, lower alkenyl, acyl, amino, lower alkoxy, lower cycloalkyloxy, aryl, aryloxy, sulfooxy, mercapto, sulfo, hydrogen, halogen, nitro, cyano or hydroxy, or may form a ring structure; Q1 is N or CH; L is optionally substituted unsaturated 3 to 10-membered heterocyclic group; X is optionally substituted monocyclic arylene or monocyclic heteroarylene; Y is -(A1)m-(A2)n-(A4)k-; Z is direct bond, -CH2-, - NH- or -O-; and R is hydrogen or lower alkyl, or a salt thereof. The compoun ds of the present invention inhibit apolipoprotein B (Apo B) secretion and are useful as a medicament for prophylactic and treatment of diseases or conditions resulting from elevated circulating levels of Apo B.
priorityDate 2000-10-05-04:00^^<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: 1406.