http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6323243-B1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-08
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C237-20
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-13
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-22
filingDate 2000-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ef9de20a3fd43f8ac3960ce706dcec87
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f8f724048a940049c648429a644c3e56
publicationDate 2001-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6323243-B1
titleOfInvention Tyrosine-derived compounds as calcium channel antagonists
abstract The present invention provides compounds that block calcium channels and have the Formula I:and pharmaceutically acceptable salts, esters, and pro-drugs thereof, whereinR1 and R2 are independently H, phenylcyclopentylcarbonyl, C1-C7 alkyl, cyclohexylmethyl, benzyl, C1-C5 alkylbenzyl, or C1-C5 alkoxybenzyl,A is -C(O)- or -CH2-;R3 is H or -CH3;R4 is C1-C4 alkyl or piperidin-1-ylethyl;R5 is phenyl-(CH2)n-, C1-C4 alkylphenyl-(CH2)n-, or halophenyl-(CH2)n-; andn is 1 or 2.The present invention also provides pharmaceutical compositions containing the compounds of Formula I and methods of using them to treat stroke, cerebral ischemia, head trauma, and epilepsy.
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priorityDate 1998-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 533.