http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2320927-A2

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00
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filingDate 2009-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0b4b1708bd8cef5a3d401c6b5b15a849
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_306a04fd195df0c469a67cc634ab9118
publicationDate 2011-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2320927-A2
titleOfInvention Modified peptides as potent inhibitors of the psd-95/nmda receptor interaction
abstract The present invention is directed to the provision of small molecule inhibitors of the PSD-95/NMDA receptor interaction, employing an undecapeptide corresponding to the C-terminal of the NMDA as a template for finding lead candidates. A compound (NMDAR/PSD-95 inhibitor) of the invention includes a peptide or peptide analogue comprising at least four peptide bonded residues having the sequence YTXV or YSXV, wherein Y is selected from among E, Q, and A, or an analogue thereof, and X is selected from among A, Q, D, N, N -Me-A, N-Me-Q, N -Me-D, and N -Me-N or an analogue thereof, wherein an amino-terminal residue of the peptide is N -alkylated. Alternatively the compound of the invention comprises a first peptide or peptide analogue linked to a second peptide or peptide analogue by a linker, where the first and second peptide or peptide analogue each comprise at least four peptide bonded residues having the sequence YTXV or YSXV, wherein Y is selected from among E, Q, and A, or an analogue thereof, and X is selected from among A, Q, D, N, N-Me-A, N -Me-Q, N-Me-D, and N -Me-N or an analogue thereof.
priorityDate 2008-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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