发明名称 PEPTIDOMIMETIC LIGANDS FOR CELLULAR RECEPTORS AND ION CHANNELS
摘要 One aspect of the present invention relates to novel peptidomimetic compounds. A second aspect of the present invention relates to the use of the novel peptidomimetic compounds as ligands - agonists or antagonists - for various cellular receptors, e.g., G-protein-coupled receptors and opioid receptors, and various cellular ion channels, e.g., sodium and calcium. In certain embodiments, compounds of the present invention preferentially or selectively inhibit sodium or calcium ion channels. In certain embodiments, compounds of the present invention preferentially or selectively agonize or antagonize DOLLAR gm opioid receptors. In certain embodiments, compounds of the present invention preferentially or selectively inhibit sodium or calcium ion channels and agonize or antagonize DOLLAR gm-opioid receptors.
申请公布号 WO0170684(A2) 申请公布日期 2001.09.27
申请号 WO2001US06173 申请日期 2001.02.27
申请人 SEPRACOR, INC.;PERSONS, PAUL, E.;HOLLAND, JOANNE, M.;HAUSKE, JAMES, R. 发明人 PERSONS, PAUL, E.;HOLLAND, JOANNE, M.;HAUSKE, JAMES, R.
分类号 C07C275/26;C07C275/28;C07C275/30;C07C275/34;C07D207/14;C07D207/16;C07D213/56;C07D217/26;C07D295/185;C07D401/12;(IPC1-7):C07D207/00 主分类号 C07C275/26
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