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filingDate 2001-09-28^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_33eef8b364cfd0fce157449c4f21ec65
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e07a25f0d668422e19ecb327d459d2a1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c2497bad230e20b5b861304069b6d86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4784560bdc19bac1e83fce8db7113f81
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7f76304633fda507e155c66f6a32d37
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4e7cf8bedfe1f5025e377f898d136d8e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_051c5a2296b9bc46263791c2fbf8ec89
publicationDate 2003-07-16^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1326835-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 compounds 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^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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