A quantitative study of [3H]D-Ala2-D-Leu5-enkephalin binding to rat brain membranes. Evidence that oxymorphone is a noncompetitive inhibitor of the lower affinity delta-binding site.

R B Rothman; W D Bowen; M Herkenham; A E Jacobson; K C Rice; C B Pert

Abstract

A quantitative study of [3H]D-Ala2-D-Leu5-enkephalin binding to rat brain membranes. Evidence that oxymorphone is a noncompetitive inhibitor of the lower affinity delta-binding site.

R B Rothman, W D Bowen, M Herkenham, A E Jacobson, K C Rice and C B Pert

Molecular Pharmacology March 1985, 27 (3) 399-409;

R B Rothman

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W D Bowen

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M Herkenham

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A E Jacobson

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K C Rice

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C B Pert

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Molecular Pharmacology

Vol. 27, Issue 3

1 Mar 1985

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Abstract

A quantitative study of [3H]D-Ala2-D-Leu5-enkephalin binding to rat brain membranes. Evidence that oxymorphone is a noncompetitive inhibitor of the lower affinity delta-binding site.

R B Rothman, W D Bowen, M Herkenham, A E Jacobson, K C Rice and C B Pert

Molecular Pharmacology March 1, 1985, 27 (3) 399-409;

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Abstract

A quantitative study of [3H]D-Ala2-D-Leu5-enkephalin binding to rat brain membranes. Evidence that oxymorphone is a noncompetitive inhibitor of the lower affinity delta-binding site.

R B Rothman, W D Bowen, M Herkenham, A E Jacobson, K C Rice and C B Pert

Molecular Pharmacology March 1, 1985, 27 (3) 399-409;

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A quantitative study of [3H]D-Ala2-D-Leu5-enkephalin binding to rat brain membranes. Evidence that oxymorphone is a noncompetitive inhibitor of the lower affinity delta-binding site.

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A quantitative study of [3H]D-Ala2-D-Leu5-enkephalin binding to rat brain membranes. Evidence that oxymorphone is a noncompetitive inhibitor of the lower affinity delta-binding site.

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