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L-nucleosides as ligands to adenosine receptors

机译:L-核苷作为腺苷受体的配体

摘要

Disclosed herein are compounds having Formula I, which are non-natural L-adenosine analogs. Also disclosed are their methods of making. Still further, disclosed are the uses of the disclosed compounds to treat cardiovascular disease, ischemia related injuries; and neurodegenerative diseases. The compounds disclosed herein have the formula:; embedded image wherein R1 and R2 are, independently, H, branched or straight-chain, substituted or unsubstituted alkyl, alkenyl, alkynyl, or aryl; R3 is branched or straight-chain, substituted or unsubstituted alkyl, hydroxy-alkyl, or —C(═O)NR6R7; and R4 and R5 are, independently, H, hydroxy, halogen, and NR8R9,wherein R6, R7, R8, and R9 are, independently, H, branched or straight-chain, substituted or unsubstituted alkyl, alkenyl, alkynyl, or aryl.
机译:本文公开了具有式I的化合物,其为非天然的L-腺苷类似物。还公开了它们的制造方法。更进一步,公开了所公开的化合物在治疗心血管疾病,局部缺血相关的损伤中的用途。和神经退行性疾病。本文公开的化合物具有下式: “嵌入式图像” 其中R 1 和R 2 独立地是H,支链或直链,取代或未取代的烷基,烯基,炔基或芳基; R 3 是支链或直链,取代或未取代的烷基,羟基烷基或-C(═O)NR 6 R 7 ;和R 4 和R 5 独立地是H,羟基,卤素和NR 8 R 9 ,其中R 6 ,R 7 ,R 8 和R 9 分别为H,分支或直链-链,取代或未取代的烷基,烯基,炔基或芳基。

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