http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1072009-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1344c5c0f7a3b561aa76dfefb893f85f
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-045
filingDate 1976-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1980-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d8e35178a4ea37fe6621f7700fd7c89d
publicationDate 1980-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1072009-A
titleOfInvention Potentiated medicaments containing antimicrobial agents
abstract Abstract of the Disclosure Antimicrobial compositions are provided wherein there is obtained an enhancement of the activity of an anti-microbial agent exemplified by quaternary ammonium compounds, bisdiguamides, anti-fungal agents, phenols, hydroxydiphenyls, carbanilides, salicylanilides, organo-metalic antiseptics, antibiotics, halogens, organic halogen derivatives and iodo-phores derived from monionic surface active agents and from polyvinylpyrrolidone by combining the antimicrobial agent with an effective amount of a potentiator. the potentiator is an alcohol or phenol derivative selected from the group consisting of (a) aliphatic straight or branched chain primary, secondary and tertiary monohydric alcohols wherin the straight chain alcohols have from about 5 to about 10 carbon atoms; and the branched chain alcohols have up to about 17 carbon atoms, their longest straight chain of carbon to carbon bonds having from about 5 to about 10 carbon atoms; (b) a primary, secondary or tertiary cyclohexylalkanol or alkylcyclohexyl-alkanol where the alkanol is as more fully defined herein-after; (c) a primary, secondary or tertiary phenylalkanol, halophenylalkanol or C1 to C3 alkylphenylalkanol where the alkanol has from about 3 to about 9 carbon atoms; and (d) a cyclohexyl phenol which may have a substituent on the phenyl ring selected form the group consisting of C1 to C3 alkyl and alkoxy, hydroxy, halo, amino and alkyl and dialkyl amino-substituents.
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priorityDate 1976-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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