http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2223926-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_baee372c55802742f9582e25c15ff11a
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-65583
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6558
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-661
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-10
filingDate 2008-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9c8e772a466cdd179239417be1c422fe
publicationDate 2010-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2223926-A1
titleOfInvention Pyridine derivative substituted with heterocycle and phosphonoxymethyl group and antifungal agent containing the same
abstract The present invention provides antifungal agents that have excellent antifungal action, and is also excellent in terms of its properties, particularly its solubility in water and its safety. According to the present invention, disclosed are compounds represented by the following formula (I):n n(wherein R 1 represents a hydrogen atom, a halogen atom, an amino group, R 11 -NH-(wherein R 11 represents a C 1-6 alkyl group, a hydroxy C 1-6 alkyl group, a C 1-6 alkoxy C 1-6 alkyl group, or a C 1-6 alkoxycarbonyl C 1-6 alkyl group), R 12 -(CO)-NH- (wherein R 12 represents a C 1-6 alkyl group or a C 1-6 alkoxy C 1-6 alkyl group), a C 1-6 alkyl group, a hydroxy C 1-6 alkyl group, a cyano C 1-6 alkyl group, a C 1-6 alkoxy group, or a C 1-6 alkoxy C 1-6 alkyl group; nR 2 represents a hydrogen atom, a C 1-6 alkyl group, an amino group, or a di-C 1-6 alkylamino group; none of X and Y represents a nitrogen atom, and the other represents a nitrogen atom or an oxygen atom; nring A represents a 5- or 6-member heteroaryl ring or a benzene ring, which may have one or two halogen atoms or C 1-6 alkyl groups; nZ represents a single bond, a methylene group, an ethylene group, an oxygen atom, a sulfur atom, -CH 2 O- -OCH 2 -, -NH-, -CH 2 NH-, -NHCH 2 -, -CH 2 S-, or -SCH 2 -; nR 3 represents a hydrogen atom or a halogen atom, or a C 1-6 alkyl group, a C 3 - 8 cycloalkyl group, a C 6-10 aryl group, a 5- or 6-member heteroaryl group, or a 5- or 6-member non-aromatic heterocyclic group, wherein these groups may have one or two substituents selected from a substituent group α; and nR 4 represents a hydrogen atom or a halogen atom; n[substituent Group α] na halogen atom, a cyano group, a C 1-6 alkyl group, a C 1-6 alkoxy group, a C 1-6 alkoxycarbonyl group, a C 3-8 cycloalkyl group, a C 2-6 alkenyl group, and a C 2-6 alkynyl group).
priorityDate 2007-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127732581
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID229173796
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID68651734
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11177
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128035868
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID247629916
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18594011
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128391806
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID163781067
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID45051774
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID229419058
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6405
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID229476236
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129150992
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128446718
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID229419194
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128404680
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6552009
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID68651733
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11124
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128551806
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12056233
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226416767
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129969390
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID68627726
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129366270
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID229415855
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226397879
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129273733
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7358
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID248860571
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127783789
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8164
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12296
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226411266
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226823891
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9746

Total number of triples: 645.