chemistry chemdraw filechemistry mol file;are useful as inhibitors of mitochondrial F1F0 ATP hydrolase, wherein R1, R5 and R7 are optional substituents, R2, R3 and R4 are hydrogen, alkyl, or substituted alkyl, or comprise a bond to R, T or Y; Z and Y are selected from C(O), CO2, SO2, CH2, CH2C(O), and C(O)C(O), or Z may be absent; R and T are CH2, C(O), or CH(CH2)p(Q), wherein Q is NR10R11, OR10 or CN and p is 0, 1 or 2; R6 is alkyl, alkenyl, substituted alkyl, substituted alkenyl, aryl, cycloalkyl, heterocyclo, or heteroaryl; R10 and R11 are hydrogen, alkyl, or substituted alkyl; and r and t are 0 or 1."/> Benzodiazepine inhibitors of mitochondial F1F0 ATP hydrolase and methods of inhibiting F1F0 ATP hydrolase
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Benzodiazepine inhibitors of mitochondial F1F0 ATP hydrolase and methods of inhibiting F1F0 ATP hydrolase

机译:线粒体F1F0 ATP水解酶的苯二氮卓抑制剂和抑制F1F0 ATP水解酶的方法

摘要

Compounds having the formula (I), chemistry chemdraw filechemistry mol file;are useful as inhibitors of mitochondrial F1F0 ATP hydrolase, wherein R1, R5 and R7 are optional substituents, R2, R3 and R4 are hydrogen, alkyl, or substituted alkyl, or comprise a bond to R, T or Y; Z and Y are selected from C(O), CO2, SO2, CH2, CH2C(O), and C(O)C(O), or Z may be absent; R and T are CH2, C(O), or CH(CH2)p(Q), wherein Q is NR10R11, OR10 or CN and p is 0, 1 or 2; R6 is alkyl, alkenyl, substituted alkyl, substituted alkenyl, aryl, cycloalkyl, heterocyclo, or heteroaryl; R10 and R11 are hydrogen, alkyl, or substituted alkyl; and r and t are 0 or 1.
机译:具有式(I)的化合物, <图像文件=“ US20040009972A1-20040115-C00001.GIF” he =“ 144.72675” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 198.02475” /> 化学chemdraw文件 化学mol文件< / ExternalFileRef> ;可用作线粒体F 1 F 0 ATP水解酶的抑制剂,其中R 1 ,R 5 和R 7 是可选的取代基,R 2 ,R 3 和R 4 是氢,烷基或取代的烷基,或包含与R,T或Y的键; Z和Y选自C(O),CO 2 ,SO 2 ,CH 2 ,CH 2 C(O)和C(O)C(O)或Z可能不存在; R和T为CH 2 ,C(O)或CH(CH 2 p (Q),其中Q为NR 10 R 11 ,OR 10 或CN,且p为0、1或2; R 6 是烷基,烯基,取代的烷基,取代的烯基,芳基,环烷基,杂环或杂芳基; R 10 和R 11 是氢,烷基或取代的烷基;和r和t为0或1。

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