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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H15-16
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-16
filingDate 1973-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1974-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_38f2cf4272d73c58c42b15884f743bb4
publicationDate 1974-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3856943-A
titleOfInvention Compositions and process
abstract THE ZWITTERION THEREOF OR THE HEMI-SALT THEREOF; R is alkyl of not more than 4 carbon atoms; and R1 is alkyl of not more than 8 carbon atoms in association with a pharmaceutical carrier. The compounds have clindamycin-like antibacterial activity and provide particularly high concentrations of compound in the urinary tract thereby being particularly useful in treating bacterial infections of the upper and lower urinary tract as well as L-forms in the kidney. OR THE ACID ADDITION SALTS THEREOF WHEREIN Halo is chlorine, bromine, or iodine, X is a member selected from the group consisting of hydrogen, an acyl radical of an aliphatic carboxylic acid having from 2 to 18 carbon atoms, inclusive, 1''-( Beta -Hydroxyethyl)-1''-demethylclindamycin compounds of the formula:
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