Conformationally restricted peptides as tools in opioid receptor studies

Current Medicinal Chemistry

Volumn 12, Issue 4, 2005, Pages 471-481

  Janecka, Anna ^a   Kruszynski, Rafal ^a,b  

^a MEDICAL UNIVERSITY OF LODZ   (Poland)

^b LODZ UNIVERSITY OF TECHNOLOGY   (Poland)

Author keywords

Agonists and antagonists; Opioid peptides; Receptor binding; Receptor selectivity; Structure activity relationships

Indexed keywords

2',6' DIMETHYLPHENYLALANINE; 2',6' DIMETHYLTYROSINE; BETA CASOMORPHINE; DELTA OPIATE RECEPTOR; DELTA OPIATE RECEPTOR AGONIST; DELTORPHIN; DERMORPHIN; DYNORPHIN A DERIVATIVE; ENDOMORPHIN 2; ENDORPHIN DERIVATIVE; ENKEPHALIN; KAPPA OPIATE RECEPTOR; LANTHIONINE; LEUCINE ENKEPHALIN; MORPHICEPTIN; MORPHICEPTIN DERIVATIVE; MU OPIATE RECEPTOR; MU OPIATE RECEPTOR AGONIST; OCTREOTIDE; OPIATE AGONIST; OPIATE ANTAGONIST; OPIATE PEPTIDE; OPIATE RECEPTOR; PENICILLAMINE; PHENYLALANINE DERIVATIVE; SOMATOSTATIN RECEPTOR; TYROSINE DERIVATIVE; TYROSYL DEXTRO ARGINYLGLYCYL 4 NITROPHENYLALANYLPROLINAMIDE; TYROSYLCYCLO[DEXTRO CYSTEINYLPHENYLALANYL DEXTRO PENICILLAMINE]; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ALKYLATION; AMINO TERMINAL SEQUENCE; ANTINOCICEPTION; BINDING SITE; CARBOXY TERMINAL SEQUENCE; CYCLIZATION; DRUG ANTAGONISM; DRUG CONFORMATION; DRUG DESIGN; DRUG POTENCY; DRUG RECEPTOR BINDING; DRUG SELECTIVITY; DRUG STABILITY; DRUG SYNTHESIS; IC 50; IN VIVO STUDY; ISOMERIZATION; LIPOPHILICITY; METHYLATION; RECEPTOR AFFINITY; REVIEW; STRUCTURE ACTIVITY RELATION;

EID: 14544294044     PISSN: 09298673     EISSN: None     Source Type: Journal    
DOI: 10.2174/0929867053362983     Document Type: Review

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