
Journal of Medicinal Chemistry p. 993 - 996 (1982)
Update date:2022-08-03
Topics:
Horn, A. S.
Griever-Kazemier, H.
Dijkstra, D.
The synthesis of four prodrug diesters (diacetyl, diisobutyryl, dipivaloyl, and dibenzoyl) of the potent dopaminergic agonist 2-amino-6,7-dihydroxytetrahydronaphthalene (6,7-ADTN) is described.The effects of prodrug structure on the levels of 6,7-ADTN in the rat corpus striatum and cerebellum, as well as the levels of the metabolite, 6-hydroxy-7-methoxy-2-aminotetralin, in the corpus striatum, have been determined after intraperitoneal administration.In addition, the stratial levels of 6,7-ADTN after administration of the dibenzoyl analogue via intraperitoneal, subcutaneous, and oral routes have been measured.These prodrugs produce a significant improvement in the penetration and accumulation of 6,7-ADTN in the brain.
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Doi:10.1016/0040-4039(91)80848-Z
(1991)Doi:10.1002/hlca.19820650142
(1982)Doi:10.1016/S0008-6215(00)80683-7
(1982)Doi:10.1016/0040-4020(81)80015-4
(1981)Doi:10.1021/jo00139a017
(1982)Doi:10.1016/S0022-328X(00)89118-4
(1982)