Topographically designed analogues of [D-Pen,D-Pen5]enkephalin

DOI: 10.1021/jm00110a010

Source and publish data:

Journal of Medicinal Chemistry p. 1823 - 1830 (1991)

Update date:2022-08-03

Topics:

Authors:

Hruby Hruby

Toth Toth

Gehrig Gehrig

Kao Kao

Knapp Knapp

Lui Lui

Yamamura

Kramer Kramer

Davis Davis

Burks Burks

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Article abstract of DOI:10.1021/jm00110a010

The conformationally restricted, cyclic disulfide-containing δ opioid receptor selective enkephalin analogue [D-Pen²,D-Pen⁵]enkephalin (1, DPDPE) was systematically modified topographically by addition of a methyl group at either the

Full text of DOI:10.1021/jm00110a010

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