Endomorphin analogs

Current Medicinal Chemistry

Volumn 14, Issue 30, 2007, Pages 3201-3208

  Janecka, Anna ^a   Staniszewska, Renata ^a   Fichna, Jakub ^a  

^a MEDICAL UNIVERSITY OF LODZ   (Poland)

Author keywords

Bioactive conformation; Opioid agonists and antagonists; Peptide stability; Structure activity relationshiops

Indexed keywords

1 AMINOCYCLOHEXANECARBOXYLIC ACID; 1,2,3,4 TETRAHYDRO 3 ISOQUINOLINE CARBOXYLIC ACID; 2 AMINOCYCLOPENTANE 1 CARBOXYLIC ACID; ANALGESIC AGENT; ANTANAL 1; ANTANAL 2; BIPHALIN; CYCLO(TYROSYL DEXTRO PROLYL DEXTRO TRYPTOPHYLPHENYLALANYLGLYCYL); CYCLOLEUCINE; DELTA OPIATE RECEPTOR ANTAGONIST; ENDOMORPHIN 1; ENDOMORPHIN 2; ENDORPHIN DERIVATIVE; KAPPA OPIATE RECEPTOR; MORPHICEPTIN; MORPHINE; MU OPIATE RECEPTOR AGONIST; MU OPIATE RECEPTOR ANTAGONIST; OPIATE AGONIST; OPIATE ANTAGONIST; OPIATE DERIVATIVE; TYROSYLCYCLO(ASPARTYLPHENYLALANYLPHENYLALANYLLYSYL)AMIDE; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ANALGESIC ACTIVITY; BLOOD BRAIN BARRIER; CHEMICAL MODIFICATION; DRUG BIOAVAILABILITY; DRUG CHOICE; DRUG CONFORMATION; DRUG DEPENDENCE; DRUG POTENCY; DRUG POTENTIATION; DRUG STRUCTURE; DRUG SYNTHESIS; DRUG TOLERANCE; GASTROINTESTINAL TOXICITY; HUMAN; NONHUMAN; PAIN; RESPIRATION DEPRESSION; REVIEW; SIDE EFFECT; STRUCTURE ACTIVITY RELATION; STRUCTURE ANALYSIS; UNSPECIFIED SIDE EFFECT;

ANIMALS; BIOLOGICAL AVAILABILITY; HUMANS; OPIOID PEPTIDES; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 37549071395     PISSN: 09298673     EISSN: None     Source Type: Journal    
DOI: 10.2174/092986707782793880     Document Type: Review

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