http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2016095870-A1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-675
filingDate 2015-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c4e46a520c77a9daf6d8e7ce279cb533
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e435cb2b10a347c9080c35c508dacc83
publicationDate 2016-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2016095870-A1
titleOfInvention Methods of forming cyclopirox or derivatives thereof in a subject by administration of prodrug
abstract A method of forming a compound in a subject can include: providing a composition having a prodrug compound represented by a structure of Formula 1 or stereoisomer thereof or pharmaceutically acceptable salt thereof; and administering the composition to a subject such that the prodrug compound has a phosphoryloxyalkyl prodrug moiety removed therefrom to form the compound in the subject and to form the separate phosphoryloxyalkyl compound. The prodrug can be included in a pharmaceutical composition for use in treatment of fungus, various cancers (e.g., bladder, breast, etc.), dermatitis, superficial mycoses; inflammation, tinea pedis, tinea cruris, and tinea corporis, Trichophyton rubrum, Trichophyton mentagrophytes, Epidermophyton floccosum , and Microsporum canis , candidiasis (moniliasis), Candida albicans , tinea (pityriasis) vesicolor, Malassezia furfur , acute myeloid leukemia, acute lymphoid leukemia, chronic myelogenous leukemia, lymphoma or multiple myeloma.
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priorityDate 2010-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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