Cyclic peptide compound, and preparation method, pharmaceutical composition and use thereof
AssigneeHangzhou Guanyu Bio-Medical Co., Ltd.
InventorsSheng Jiang, Zhiyi Yao, Yiwu Yao, Yatao Qiu, Changyin Lu, Kun Su, Xiaoming Yao
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Abstract
The present invention relates to a cyclic peptide compound, and a preparation method, pharmaceutical composition and use thereof. In particular, the cyclic peptide compound of the present invention has a structure as shown by general formula (I). The compound of general formula (I), and isomers, racemates, pharmaceutically acceptable salts, crystalline hydrates, solvates or mixtures thereof have a use in the preparation of medicaments for preventing or treating mammalian diseases associated with histone deacetylase dysregulations.
Claims10
A compound with a chemical structure shown as formula (I), its isomers, racemates, pharmaceutically acceptable salts, crystalline hydrate, and solvate or their mixture:
- wherein,
- R1 is hydrogen, C1-16 alkyl, C3-16 cycloalkyl, —(C═O)—(C1-16 alkyl), —(C═S)—(C1-16 alkyl) or —S—(C1-16 alkyl);
- R2 is hydrogen, C1-12 alkyl, —CH2—O—(C1-12 alkyl), —CH2—NH—(C1-12 alkyl), —CH2—S—(C1-12 alkyl), C6-12 aryl, heteroaryl, —CH2—(C6-12 aryl) or —CH2-heteroaryl;
- wherein the C6-12 aryl, heteroaryl, —CH2—C6-12 aryl, and —CH2-heteroaryl, optionally comprise one or more substituents and the one or more substituents are selected from halo, amino, hydroxyl, nitro, cyano, C1-12 alkyl, C1-12 alkoxy, amino C1-12 alkyl, acyl, acyloxy, thio C1-12 alkyl, carboxyl and phenyl;
- R3, R4 are independently selected from hydrogen, C1-12 alkyl, —O—(C1-12 alkyl), —NH—(C1-12 alkyl), —S—(C1-12 alkyl), C6-12 aryl and heteroaryl;
- X is N and Y is C, or both X and Y are N;
- R5, R6, R7 are independently selected from hydrogen, halo, —S—(C1-12 alkyl), C1-12 alkyl and t-butoxycarbonyl;
- Z is —CH2—, —NH—, —O—, —S— or
- m is 0, 1, 2, 3, 4, 5 or 6.
Dependencies are inferred from the claim text.