Halogenated mazindol analogs as potential inhibitors of the cocaine binding site at the dopamine transporter.
Halogenated mazindol analogs as potential inhibitors of the cocaine binding site at the dopamine transporter.
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卤化马吲哚类似物作为多巴胺转运蛋白上可卡因结合位点的潜在抑制剂。
DOI:
10.1021/jm960288w
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发表时间:
1996
期刊:
影响因子:
--
通讯作者:
Kuhar,MJ
中科院分区:
文献类型:
--
作者:
Houlihan,WJ;Boja,JW;Parrino,VA;Kopajtic,TA;Kuhar,MJ
A series of halogenated (F, Cl, Br, I), pyrimido and diazepino homologs of mazindol were prepared and evaluated for their ability to displace [3H]WIN 35,428 binding and to inhibit uptake of [3H]dopamine (DA) in rat striatal tissue. All of the compounds except for the 2‘-chloro (6) and 2‘-bromo (16) analogs of mazindol displaced [3H]WIN 35,428 binding and inhibited [3H]DA uptake more effectively than (R)-cocaine. Structure−activity studies indicated that best inhibition of [3H]WIN 35,428 binding occurred in the imidazo series with compounds containing one or two Cl or Br atoms in the 3‘- or 4‘-position of the free phenyl group. Replacement of the imidazo ring by a pyrimido or diazepino ring enhanced binding inhibition. The most potent inhibitors of [3H]WIN 35,428 binding and [3H]DA uptake were 6-(3‘-chlorophenyl)-2,3,4,6-tetrahydropyrimido[2,1-a]isoindol-6-ol (23; IC501.0 nM; 8× mazindol) and 7-(3‘,4‘-dichlorophenyl)-2,3,4,5-tetrahydro-7H-diazepino[2,1-a]isoindol-7-ol (28; IC500.26 nM; 32× mazindol), respectively. No significant differences was found between binding and uptake inhibition. Mazindol and the pyrimido and diazepino homologs24and27showed a selectivity for the DA uptake over the serotonin (5-HT) uptake site of 5-, 250-, and 465-fold, respectively, and displayed weak or no affinity for a variety of neurotransmitter receptor sites.