http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2380597-A1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K51-08
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filingDate 2010-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4e338f12030861cd2f16908bf34a718e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c02c7fb6b691ad29e8170cb6f37187c9
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a4fcbcfb71bdf376c1080bcae36ab0da
publicationDate 2011-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2380597-A1
titleOfInvention Cyclopeptide derivatives and uses thereof
abstract The invention relates to compounds having a structure according to formula (I), cyclo[(R 1 )Xaa 1 -B-(R 2 )Xaa 2 -(R 3 )Xaa 3 -(R 4 )Xaa 4 ], or pharmaceutically acceptable salts thereof, wherein Xaa 1 and Xaa 3 are independently of each other, a natural or unnatural amino acid, preferably with Xaa 1 and Xaa 3 being, independently of each other, an amino acid comprising an aromatic moiety in its side chain, Xaa 2 is a natural or unnatural basic amino acid, Xaa 4 is glycine or a D-amino acid, R 1 , R 2 , R 3 and R 4 are independently of each other H or methyl, B is an amino acid group having a structure according to formula (II), -N(-Q)-CHR 5 -C(=O)-, wherein R 5 is selected from the group consisting of H, optionally substituted alkyl, optionally substituted aryl and optionally substituted heteroaryl, and a moiety L, and wherein Q is a group being sterically more demanding than a methyl group. The invention also relates to compositions, methods and uses related to said compounds.
priorityDate 2010-04-20-04:00^^<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: 550.