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filingDate 1994-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6197b6dfea68b4385daa65e8afc55e20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3faa2dc216b5c4e56285248ab9e968b7
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publicationDate 1995-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H07330791-A
titleOfInvention Novel 16-membered ring macrolide derivative and new comprehensive production method thereof
abstract (57) [Summary] (Modified) [Purpose] A novel 16-position in which the 3-position is a free hydroxyl group, the 3 "-position tertiary hydroxyl group is methylated, and the 4" -position hydroxyl group is acylated. Provided are a membered-ring macrolide derivative, a novel production method thereof, and a compound useful as an antibacterial agent itself. [Structure] Starting from a known naturally-occurring 16-membered macrolide antibiotic represented by the general formula (II), the 3-position is a free hydroxyl group, and the 3 "-position tertiary hydroxyl group is methylated. A novel 16-membered macrolide derivative represented by the general formula (I), which is useful as an antibacterial agent and has a hydroxyl group at the 4 "position and is acylated, was chemically synthesized.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100361397-B1
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