http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2331352-T3

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filingDate 2002-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7055d18fb82102223daeb850cc69ff6f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6dc91b9d3cae805086bfc4abf28233bc
publicationDate 2009-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2331352-T3
titleOfInvention INHIBITORS BASED ON 2,1-OXAZOLINE AND 1,2-PIRAZOLINE FROM DIPEPTIDIL PEPTIDASA IV AND ITS USE.
abstract A compound that has the structure ** (See formula) ** n is 0 or 1; -X is CN; Y is N, NH or O; Z is CH or CH2, where Z CH2 is when Y is O or NH, with YZ forming a single bond, and Z being Z when Y is N, with YZ forming a double bond R1, R2, R3 and R4 are the same or different and are independently selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, bicycloalkyl, bicycloalkylalkyl, alkylthioalkyl, arylalkylthioalkyl, cycloalkenyl, aryl, aralkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl, optionally substituted by all 1-carbonyl-alkyl, cycloheteroalkyl with all carbon atoms; , 3, 4 or 5 groups selected from hydrogen, halogen, alkyl, polyhalogenoalkyl, alkoxy, halogenoalkoxy, polyhalogenoalkoxy, alkoxycarbonyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, polycycloalkyl, heteroarylamino, arylamino, cycloheteroalkyl, cycloheteroalkyloxy, nitroxyalkyloxy, nitroxyalkyloxy, nitroxyalkyloxy, nitroxyalkyloxy, nitroxyalkyloxy, nitroalkyloxy , amino, substituted amino, alkylamino, dialkylamino, thiol, alkylthio, alkylcarbonyl, acyl , alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, alkylaminocarbonyl, alkenylaminocarbonyl, alkylcarbonyloxy, alkylcarbonylamino, arylcarbonylamino, alkylsulfonylamino, alkylaminocarbonylamino, alkoxycarbonylamino, alkylsulfonyl, aminosulfonyl, alkylsulfinyl sulfonyl; and R1 and R3 can optionally be taken together to form - (CR5R6) m- in which m is from 2 to 6, and R5 and R6 are the same or different and are independently selected from hydroxy, alkoxy, H, alkyl, alkenyl, alkynyl , cycloalkyl, cycloalkylalkyl, cycloalkenyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl, cycloheteroalkylalkyl, alkylcarbonylamino, arylcarbonylamino, alkoxycarbonylamino, aryloxycarbonylamino, alkoxycarbonyla, aryloxycarbonyl, or R8 may together take R4 to take 8 which p is 3 to 6, and R7 and R8 are the same or different and are independently selected from hydroxy, alkoxy, cyano, H, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, cycloalkenyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloheteroalkyl , cycloheteroalkylalkyl, alkylcarbonylamino, arylcarbonylamino, alkoxycarbonylamino, aryloxycarbonylamino, alkoxycarbonyl, aryloxycarbonyl or, or alkylaminocarbonylamino, or optionally R1 and R3 together with ** (See formula) ** form a 5 to 7 member ring containing a total of 2 to 4 heteroatoms selected from N, O, S, SO or SO2; or optionally R1 and R3 together with ** (See formula) ** form a 4 to 8 membered cycloheteroalkyl ring in which the cycloheteroalkyl ring has an optional aryl ring fused thereto, or a 3 to cycloalkyl ring 7 members optional condensed thereto; including all its stereoisomers; and its pharmaceutically acceptable salts.
priorityDate 2001-04-12-04:00^^<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/SID419483452
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID681
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419533103
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5745206
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID84003
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422601242

Total number of triples: 612.