http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4714757-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_76195fd1cd08192222699d8e7a88c231
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K5-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-02
filingDate 1985-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1987-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_613eed73ccd287298af5520db8cc2146
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b94e579e1a329b8c229323aeaf904015
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1809e327e6e16100fd07d7ce9b1b2538
publicationDate 1987-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4714757-A
titleOfInvention Aminopeptidase inhibitors
abstract Aminopeptidase inhibitory activity is exhibited by compounds having the formula <IMAGE> and pharmaceutically acceptable salts thereof, wherein R1 and R2 are each independently hydrogen, alkyl, carboxyalkyl, halo-substituted alkyl, hydroxyalkyl, aminoalkyl, mercaptoalkyl, alkylthioalkyl, (cycloalkyl)alkyl, (heteroaryl)alkyl, arylalkyl, carbamoylalkyl, guanidinylalkyl or heteroaryl; R3 is hydrogen, alkyl, cycloalkyl, aryl, heteroaryl, arylalkyl, (heteroaryl)alkyl, <IMAGE> +TR CH2NR4R5; R4 and R5 are each independently hydrogen, alkyl, cycloalkyl, aryl, heteroaryl, arylalkyl, or (heteroaryl)alkyl; A is glycyl, alanyl, leucyl, phenylalanyl, arginyl, sarcosyl, seryl, asparagyl, lysyl, glutamyl, histidyl, tryptophyl, cysteinyl, methionyl, threonyl, tyrosyl, valyl, aspartyl, prolyl, norleucyl, or norvalyl; and n is an integer of 1 to 6.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5444042-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7205435-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2004176333-A1
priorityDate 1985-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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