7-Benzylidenenaltrexone (BNTX): A selective δ1 opioid receptor antagonist in the mouse spinal cord

Life Sciences

Volumn 52, Issue 8, 1993, Pages 769-775

  Sofuoglu, Mehmet ^a   Portoghese, P S ^a   Takemori, A E ^b  

^a UNIVERSITY OF MINNESOTA   (United States)

^b UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3,4 DICHLORO N METHYL N [2 (1 PYRROLIDINYL)CYCLOHEXYL]BENZENEACETAMIDE METHANESULFONATE; 7 BENZYLIDENENALTREXONE; DELTA OPIATE RECEPTOR; DELTORPHIN II [2 DEXTRO ALANINE]; ENKEPHALIN[2 DEXTRO ALANINE 4 METHYLPHENYLALANINE 5 GLYCINE]; ENKEPHALIN[2,5 DEXTRO PENICILLAMINE]; MORPHINE; OPIATE AGONIST; OPIATE ANTAGONIST; RECEPTOR SUBTYPE; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANTINOCICEPTION; ARTICLE; CONTROLLED STUDY; DRUG ANTAGONISM; DRUG SELECTIVITY; INTRATHECAL DRUG ADMINISTRATION; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; SPINAL CORD; SUBCUTANEOUS DRUG ADMINISTRATION; TAIL FLICK TEST;

ANALGESICS; ANIMAL; BENZYLIDENE COMPOUNDS; ENKEPHALIN, ALA(2)-MEPHE(4)-GLY(5)-; ENKEPHALIN, D-PENICILLAMINE (2,5)-; ENKEPHALINS; MALE; MICE; NALTREXONE; NARCOTIC ANTAGONISTS; OLIGOPEPTIDES; RECEPTORS, OPIOID, DELTA; SPINAL CORD; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0027463858     PISSN: 00243205     EISSN: None     Source Type: Journal    
DOI: 10.1016/0024-3205(93)90240-4     Document Type: Article

References (17)

1. Application of the message-address concept in the design of highly potent and selective non-peptide .delta. opioid receptor antagonists