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首页> 外文期刊>Medicinal chemistry >Synthesis and pharmacological evaluation of 4-phenoxy-1,2,3,4-tetrahydroisoquinolines and 4,5,6,6a-tetrahydrochromeno(2,3,4-de)isoquinolines.
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Synthesis and pharmacological evaluation of 4-phenoxy-1,2,3,4-tetrahydroisoquinolines and 4,5,6,6a-tetrahydrochromeno(2,3,4-de)isoquinolines.

机译:4-苯氧基-1,2,3,4-四氢异喹啉和4,5,6,6a-四氢色素(2,3,4-de)异喹啉的合成及药理学评价。

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摘要

The novel 4-phenoxy-1,2,3,4-tetrahydroisoquinolines 6a-c and their rigid congeners 4,5,6,6a-tetrahydro-chromeno[2,3,4-de]isoquinolines 7a,b were synthesized in order to obtain dopamine D2-like receptor ligands. The new compounds were evaluated for their in vitro binding affinities, in vivo behavioral activities on rats, and for their effects on rat brain neurochemistry. Compounds 6b (toward both D2 and D3 dopamine receptors) and 7a,b (toward D3 only dopamine receptors) showed the most significant affinities. However none of the new compounds was able to stimulate behavioral activity in non pre-treated rats, nor to influence brain neurochemistry.
机译:依次合成了新颖的4-苯氧基-1,2,3,4-四氢异喹啉6a-c及其刚性同系物4,5,6,6a-四氢-铬诺[2,3,4-de]异喹啉7a,b获得多巴胺D2样受体配体。评价了新化合物的体外结合亲和力,对大鼠的体内行为活性以及对大鼠脑神经化学的影响。化合物6b(针对D2和D3多巴胺受体)和7a,b(仅针对D3多巴胺受体)显示出最显着的亲和力。然而,这些新化合物均未能够刺激未预处理大鼠的行为活性,也不会影响脑神经化学。

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