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CARBAMINIC ACID DERIVED CONTENT OF AN AMID GROUP AS HDAC INHIBITOR

机译:作为HDAC抑制剂的酰胺基的氨基甲酸来源

摘要

This invention pertains to certain active carbamic acid compounds which inhibit HDAC activity and which have the following formula: CHEM wherein: A is an aryl group; Q1 is an aryl leader group having a backbone of at least 2 carbon atoms; J is an amide linkage selected from: -NR1C(=O)- and -C(=O)NR1-; R1 is an amido substituent; and, Q2 is an acid leader group; and pharmaceutically acceptable salts, solvates, amides, esters, ethers, chemically protected forms, and prodrugs thereof, for use in the treatment of parasitic infections, such as malaria.
机译:本发明涉及抑制HDAC活性并具有下式的某些活性氨基甲酸酯化合物:其中:A是芳基; Q 1为具有至少2个碳原子的主链的芳基前导基团; J是选自以下的酰胺键:-NR 1 C(= O)-和-C(= O)NR 1-。 R 1为酰胺基取代基;并且,Q 2为酸前导基团。以及药学上可接受的盐,溶剂化物,酰胺,酯,醚,其化学保护形式和前药,用于治疗寄生虫感染,例如疟疾。

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