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filingDate 1993-01-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd0333d85be156a0e6fe3bc95a6811a3
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publicationDate 1994-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H069679-A
titleOfInvention Novel 16-membered macrolide derivative with sustained antibacterial activity in plasma, its synthetic intermediate and method for producing them
abstract (57) [Summary] (Modified) [Objective] To provide a 16-membered ring macrolide compound which is useful as a bactericide per se and is also a production intermediate. [Structure] A compound represented by the formula (1) or a pharmaceutically acceptable salt thereof. A novel 16-membered macrolide compound represented by the formula (1) is produced by chemical modification using midecamycin A 3 as a starting material. [In the formula, R 1 is O, H and OH, or H and O-COR 6 R 2 and R 3 are H or —COR 6 ; R 4 Is a C 1-4 straight chain alkyl group; R 5 is C 1-10 (substituted) alkyl group and the like; R 6 is C 1-3. It is a straight-chain alkyl group]
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2000086691-A
priorityDate 1992-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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