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    • 1. 发明公开
    • PHENYL-SUBSTITUTED NICOTINIC LIGANDS, AND METHODS OF USE THEREOF
    • 尼日利亚联合王国维多利亚州立大学
    • EP2776423A4
    • 2015-01-07
    • EP12847869
    • 2012-11-09
    • UNIV GEORGETOWNUNIV DUKE
    • BROWN MILTON LPAIGE MIKELL AXIAO YINGXIANKELLAR KENNETH JYENUGONDA VENKATA MAHIDHARLEVIN EDWARD DREZVANI AMIR H
    • C07D403/06
    • C07D401/12C07D213/65
    • Disclosed are compounds and methods of using them to treat a disorder selected from the group consisting of addiction, pain, obesity, schizophrenia, epilepsy, mania and manic depression, anxiety, Alzheimer's disease, learning deficit, cognition deficit, attention deficit, memory loss, Lewy Body Dementia, Attention Deficit Hyperactivity Disorder (ADHD), Parkinson's disease, Huntington's disease, Tourette's syndrome, amyotrophic lateral sclerosis, inflammation, stroke, spinal cord injury, dyskinesias, obsessive compulsive disorder, chemical substance abuse, alcoholism, memory deficit, pseudodementia, Ganser's syndrome, migraine pain, bulimia, premenstrual syndrome or late luteal phase syndrome, tobacco abuse, post-traumatic syndrome, social phobia, chronic fatigue syndrome, premature ejaculation, erectile difficulty, anorexia nervosa, autism, mutism, trichotillomania, hypothermia, and disorders of sleep.
    • 公开了使用它们治疗选自瘾,疼痛,肥胖,精神分裂症,癫痫,躁狂和躁狂抑郁,焦虑,阿尔茨海默病,学习缺陷,认知缺陷,注意力缺陷,记忆丧失, 路易体痴呆,注意缺陷多动障碍(ADHD),帕金森病,亨廷顿病,图雷特综合征,肌萎缩性侧索硬化,炎症,中风,脊髓损伤,运动障碍,强迫症,化学物质滥用,酒精中毒,记忆缺陷,假性痴呆, 甘ser综合征,偏头痛,贪食症,经前期综合征或晚黄体期综合症,烟草滥用,创伤后综合征,社交恐惧症,慢性疲劳综合征,早泄,勃起困难,神经性厌食症,孤独症,多发症,头痛,低体温和失调 的睡眠
    • 7. 发明申请
    • 10-SUBSTITUTED CYTISINE DERIVATIVES AND METHODS OF USE THEREOF
    • 10替代的CYTISINE衍生物及其使用方法
    • WO2007115092A3
    • 2008-07-31
    • PCT/US2007065498
    • 2007-03-29
    • UNIV GEORGETOWNKOZIKOWSKI ALAN PTUECKMANTEL WERNERCHELLAPPAN SHEELAKELLAR KENNETH JXIAO YINGXIAN
    • KOZIKOWSKI ALAN PTUECKMANTEL WERNERCHELLAPPAN SHEELAKELLAR KENNETH JXIAO YINGXIAN
    • A61K31/4375A61K31/439
    • C07D471/18
    • The present invention relates to substituted cytisine compounds that are useful in treating diseases impacted by a nicotinic ACh receptor. One aspect of the invention relates to 10-substituted cytisine compounds. In certain instances, the cytisine is substituted in the 10-position by an alkyl, aryl or aralkyl group. The present invention also relates to a pharmaceutical composition comprises the substituted cytisine compound or the 10- substituted cytisine compound. The invention also relates to a method of modulation a nicotinic ACh receptor in a mammal, comprising the step of administering to a mammal in need thereof a therapeutically effective amount of a substituted cytisine. In certain instances, the substituted cytisine is a 10-substituted cytisine. Another aspect of the present invention relates a method of treating a disease impacted by a nicotinic ACh receptor, comprising the step of administering to a mammal in need thereof a therapeutically effective amount of a substituted cytisine. In certain instances, the substituted cytisine is a 10-substituted cytisine.
    • 本发明涉及可用于治疗受烟碱性ACh受体影响的疾病的取代的仙培酮化合物。 本发明的一个方面涉及10-取代的仙客来化合物。 在某些情况下,通过烷基,芳基或芳烷基在十位置替代赤藓酸。 本发明还涉及一种药物组合物,其包含取代的赤藓苷化合物或10-取代的仙茅素化合物。 本发明还涉及一种调节哺乳动物中烟碱性ACh受体的方法,其包括向有需要的哺乳动物施用治疗有效量的取代的氰尿酸的步骤。 在某些情况下,取代的洋甘菊是一种10-取代的胞苷。 本发明的另一方面涉及一种治疗由烟碱性ACh受体影响的疾病的方法,其包括向有需要的哺乳动物施用治疗有效量的取代的氰尿酸的步骤。 在某些情况下,取代的洋甘菊是一种10-取代的胞苷。