http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1189939-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cc4209078d025bee83bc1ad02a70fcf2
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00
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filingDate 2000-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eb2bb6262ae47a6c65761a295773c04a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e4e77995b27864972fbd016c1cec6682
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4eb48d7ad2a4d0a9df3221dcd3cf9e82
publicationDate 2002-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1189939-A1
titleOfInvention Bh3 modified peptides
abstract The present invention is directed to a peptide of formula (I), as defined herein, or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising said peptide of formula (I), and the use thereof to restore apoptosis in human tumor cells. A compound of formula (I) of the present invention is R-A?1-A2-A3-A4-A5-A6-A7-A8-A9-A10-A11-A12-A13-A14-A15-NHR1¿ or a pharmaceutically acceptable salt thereof wherein, R is (C¿1?-C5)acyl; A?1¿ is absent or an aliphatic amino acid; A2 is absent or is selected from the group consisting of Gly, Ala, Ser, Thr and Asn; A?3 and A4¿ are each absent or are each a coded amino acid; A5 is an aliphatic amino acid; A6 is Ala or a basic amino acid; A7 is selected from the group consisting of Ile, Leu, Val, Ser, Thr, Lys and Arg; A8 is an aliphatic amino acid; A9 is Gly; A?10 and A11¿ are each independently Asp or Glu; A12 is an aliphatic amino acid Ile, Leu, Met and Val; A13 is Asp, Glu or Asn; A?14 and A15¿ are each independently absent or selected from the group consisting of Ile, Leu, Val, Met, Ser, Thr, Asn, Lys and Arg; and R1 is (C¿1?-C5)alkyl.
priorityDate 1999-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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