Literature DB >> 7411420

Evaluation of 2-azabicyclo[2.2..2]octane analogs of 4-anilidopiperidine analgesics.

R F Borne, S J Law, J C Kapeghian, L W Masten.   

Abstract

Eight analogs of the fentanyl-type analgesics, in which the piperidine ring is restricted into a boat conformation, were evaluated for analgesic activity. All analogs were less active than fentanyl, but interesting conformational and structural relationships were observed. Results of the study are discussed.

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Year:  1980        PMID: 7411420     DOI: 10.1002/jps.2600690934

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  3 in total

1.  Development of a conformational search strategy for flexible ligands: a study of the potent mu-selective opioid analgesic fentanyl.

Authors:  C Cometta-Morini; G H Loew
Journal:  J Comput Aided Mol Des       Date:  1991-08       Impact factor: 3.686

Review 2.  Fentanyl-related compounds and derivatives: current status and future prospects for pharmaceutical applications.

Authors:  Ruben S Vardanyan; Victor J Hruby
Journal:  Future Med Chem       Date:  2014-03       Impact factor: 3.808

3.  Conformation-activity relationships of opiate analgesics.

Authors:  J Martin; P Andrews
Journal:  J Comput Aided Mol Des       Date:  1987-04       Impact factor: 3.686

  3 in total

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