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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D521-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-60
filingDate 1978-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fc0055dd2ebf735ac9878abdf829fd5c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a26f19d41ab0b0d10929925eae051577
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_72295f5534677f89a1c777fcb48adeff
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_402a012bed4f4c370844e544aa4575ee
publicationDate 1980-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2832677-A1
titleOfInvention HYDROXYPROPYL IMIDAZOLES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS MEDICINAL PRODUCTS
abstract Imidazole derivs. of formula (I) and their acid-addn. salts are new: (R is opt. substd. phenyl, naphthyl or tetrahydronaphthyl; R1 is opt. substd. phenyl or cycloalkyl; R2 is H; or R1 + R2 in the ortho position to each other can form an opt. substd. polymethylene bridge or a fused benzene ring; R3 is halogen, alkyl, alkoxy or haloalkyl; n = 0-3). Cpds. (I) have antimycotic activity, e.g. against Candida, Epidermophyton, Aspergillus, Trichophyton, Microsporon and Penicillium spp. They can be used to treat dermatological and systemic infections in humans and animals.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11426412-B2
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priorityDate 1978-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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