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【结 构 式】

【药物名称】

【化学名称】2-[4-[2(R)-[3(S),5(R)-Dimethyl-2-oxo-1(S)-cyclohexyl]-2-hydroxyethyl]-2,6-dioxopiperidin-1-yl]acetic acid ethyl ester

【CA登记号】246257-13-6

【 分 子 式 】C19H29NO6

【 分 子 量 】367.44608

【开发单位】Friedrich-Schiller-Universität Jena (Originator), Hans Knöll Institute Natural Prod. Res. (Originator), Max-Planck-Gesellschaft (Originator)

【药理作用】Antiparkinsonian Drugs, Cerebrovascular Diseases, Treatment of, Cognition Disorders, Treatment of, Extrapyramidal Disorders, Treatment of, NEUROLOGIC DRUGS, Stroke, Treatment of, Neurotrophic Agents, Rotamase (FKBP12) Inhibitors

合成路线1

By condensation of cycloheximide (I) with ethyl 2-bromoacetate (II) by means of K2CO3 and 18-crown-6 in acetone.

1 Grabley, S.; Wyrwa, R.; Schummann, D.; Marsch, S.; Christner, C.; Küllertz, G.; Fischer, G.; Thiericke, R.; Synthesis and cytotoxic evaluation of cycloheximide derivatives as potential inhibitors of FKBP12 with neuroregenerative properties. J Med Chem 1999, 42, 18, 3615.
2 Thiericke, R.; Fischer, G.; Küllertz, G.; Christner, C.; Grabley, S.; Wyrwa, R. (Hans Knöll Institute for Natural Product Research; Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. ); Cyclohexamide derivs. which influence the regeneration of neural tissue. WO 0026188 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 38236 4-[(2R)-2-[(1S,3S,5R)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]-2,6-piperidinedione 66-81-9 C15H23NO4 详情 详情
(II) 16640 Ethyl 2-bromoacetate; Ethyl bromoacetate 105-36-2 C4H7BrO2 详情 详情
Extended Information