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Inhibitor(s) of transporters or uptake of monoaminergic neurotransmitters

机译:转运蛋白抑制剂或单胺能神经递质的吸收

摘要

The present disclosure concerns a compound, or a pharmaceutically acceptable salt thereof, having a formula:; embedded image where at least one of R1-R4 is a heterocycle, at least one of R1-R4 is an aryl group coupled to the ring by a linker atom, functional group, or other moiety, or where none of R1-R4 is an amide, and any and all combinations thereof. Remaining R1-R4 substituents independently are aliphatic, substituted aliphatic, amine, substituted amine, aryl, substituted aryl, cyclic, substituted cyclic, halide, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic, hydrogen or hydroxyl. A method for treating a subject also is provided comprising administering a disclosed compound or compounds, or a prodrug that is converted into the disclosed compound or compounds, or a composition comprising the compound, compounds, or prodrugs thereof, to a subject. A method for making disclosed compounds also is provided.
机译:本公开涉及具有下式的化合物或其药学上可接受的盐: “嵌入式图像” 其中R 1 -R 4 中的至少一个是杂环,R 1 -R 4 中的至少一个>是通过连接原子,官能团或其他部分与环相连的芳基,或者其中R 1 -R 4 都不是酰胺,并且及其所有组合。剩余的R 1 -R 4 取代基分别是脂肪族,取代的脂肪族,胺,取代的胺,芳基,取代的芳基,环状,取代的环,卤化物,杂芳基,取代的杂芳基,杂环,取代的杂环,氢或羟基。还提供了一种用于治疗受试者的方法,其包括向受试者施用所公开的一种或多种化合物,或转化成所公开的一种或多种化合物的前药,或包含该化合物,其化合物或前药的组合物。还提供了一种制备公开的化合物的方法。

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