http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2005113304-A1

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filingDate 2004-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_11ed6d066e4465122f5e525406104c56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73c00afc68e3d7db0bd0b3c4fa670bfe
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publicationDate 2005-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2005113304-A1
titleOfInvention Previns as specific inhibitors and therapeutic agents for Botulinum toxin B and Tetanus neurotoxins
abstract The compounds of the invention are generally described by the formula: n nB 1 Z* 2 B 3 Z* 4 X* 5 Q 6 F 7 X 8 X 9 X 10 X 11   (1), n nB 1 X 2 X 3 X 4 X 5 Q 6 F 7 X 8 X 9 X 10 X 11   (2), or n nB 1 Z 2 B 3 X 4 Z 5 Q 6 F 7 Z 8 X 9 X 10 X 11   (3) nand the salts, esters, amides, and acyl forms thereof. Each position represented by a letter indicates a single amino acid residue: B is a basic of polar/large amino acid or a modified form thereof; X is a small or hydrophobic amino acid or a modified form thereof; X* is a small or polar/large amino acid or a modified form thereof; Z is a polar/large or hydrophobic amino acid or a modified form thereof; Z* is Proline or a polar/large of hydrophobic amino acid or a modified form thereof. As described below, one or more of the peptide linkages between the amino acid residues may be replaced by a peptide linkage mimic. These compounds may be used as molecular building blocks to create compounds that are optimized for inhibiting the protease activity of Botulinum b and tetanus toxins.
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type http://data.epo.org/linked-data/def/patent/Publication

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