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N-methyl-4-phenyl-1,2,3,4-tetrahydro-1-naphthylamine

中文名称
——
中文别名
——
英文名称
N-methyl-4-phenyl-1,2,3,4-tetrahydro-1-naphthylamine
英文别名
N-methyl-4-phenyl-1,2,3,4-tetrahydronaphthalen-1-amine
N-methyl-4-phenyl-1,2,3,4-tetrahydro-1-naphthylamine化学式
CAS
——
化学式
C17H19N
mdl
——
分子量
237.345
InChiKey
NVXPZMLRGBVYQV-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    12
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    N-氯甲胺1,2-二氢-1-苯基萘 在 rac-QUINAP-Rh 儿萘酚硼烷diethylzinc 作用下, 以 甲苯乙醚 为溶剂, 反应 2.0h, 以47%的产率得到N-methyl-4-phenyl-1,2,3,4-tetrahydro-1-naphthylamine
    参考文献:
    名称:
    Efficient kinetic resolution in hydroboration of 1,2-dihydronaphthalenes
    摘要:
    1-取代的1,2-二氢萘在与Rh–QUINAP复合物进行不对称氢硼化过程中发生动力学分离。
    DOI:
    10.1039/b111175b
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文献信息

  • [EN] 5-HT2C RECEPTOR AGONISTS AND COMPOSITIONS AND METHODS OF USE<br/>[FR] AGONISTES DE RÉCEPTEUR 5-HT2C ET COMPOSITIONS ET PROCÉDÉS D'UTILISATION
    申请人:ARENA PHARM INC
    公开号:WO2017023679A1
    公开(公告)日:2017-02-09
    Provided in some embodiments are compounds of Formula A, as defined herein, that modulate the activity of 5-HT2C receptor. Also provided in some embodiments are methods, such as, for weight management, inducing satiety, and decreasing food intake, and for preventing and treating obesity, antipsychotic-induced weight gain, type 2 diabetes, Prader-Willi syndrome, tobacco/nicotine dependence, drug addiction, alcohol addiction, pathological gambling, reward deficiency syndrome, and sex addiction), obsessive-compulsive spectrum disorders and impulse control disorders (including nail-biting and onychophagia), sleep disorders (including insomnia, fragmented sleep architecture, and disturbances of slow-wave sleep), urinary incontinence, psychiatric disorders (including schizophrenia, anorexia nervosa, and bulimia nervosa), Alzheimer disease, sexual dysfunction, erectile dysfunction, epilepsy, movement disorders (including parkinsonism and antipsychotic-induced movement disorder), hypertension, dyslipidemia, nonalcoholic fatty liver disease, obesity-related renal disease, and sleep apnea.
    在某些实施例中提供了一些符合本文所定义的A式化合物,其调节5-HT2C受体的活性。在某些实施例中还提供了一些方法,例如用于体重管理、诱导饱腹感、减少食物摄入,以及预防和治疗肥胖、抗精神病药物引起的体重增加、2型糖尿病、普拉德-威利综合征、烟草/尼古丁依赖、药物成瘾、酒精成瘾、病理性赌博、奖赏缺乏综合征和性成瘾,强迫症谱系障碍和冲动控制障碍(包括咬指甲和咬甲症),睡眠障碍(包括失眠、睡眠结构碎裂和慢波睡眠紊乱),尿失禁,精神障碍(包括精神分裂症、厌食症和暴食症),阿尔茨海默病,性功能障碍,勃起功能障碍,癫痫,运动障碍(包括帕金森病和抗精神病药物引起的运动障碍),高血压,血脂异常,非酒精性脂肪肝病,肥胖相关肾脏疾病和睡眠呼吸暂停症。
  • [EN] NEGATIVE ALLOSTERIC MODULATORS OF METABOTROPIC GLUTAMATE RECEPTOR 2<br/>[FR] MODULATEURS ALLOSTÉRIQUES NÉGATIFS DU RÉCEPTEUR MÉTABOTROPIQUE DU GLUTAMATE DE TYPE 2
    申请人:UNIV VANDERBILT
    公开号:WO2016149324A1
    公开(公告)日:2016-09-22
    Described are negative allosteric modulators of metabotropic glutamate receptor 2 (mGlu2), pharmaceutical compositions including the compounds, and methods of using the compounds and compositions for treating depression, anxiety, obsessive-compulsive disorder, cognitive disorders, Alzheimer's disease, or autism spectrum disorders in a subject.
    描述了代谢型谷氨酸受体2(mGlu2)的负变构调节剂,包括这些化合物的药物组合物,以及使用这些化合物和组合物治疗受试者的抑郁症、焦虑症、强迫症、认知障碍、阿尔茨海默病或自闭症谱系障碍的方法。
  • [EN] 5-HT2C RECEPTOR AGONISTS AND COMPOSITIONS AND METHODS OF USE<br/>[FR] AGONISTES DU RÉCEPTEUR 5-HT2C ET COMPOSITIONS ET PROCÉDÉS D'UTILISATION
    申请人:ARENA PHARM INC
    公开号:WO2015066344A1
    公开(公告)日:2015-05-07
    Provided are 5-HT2C receptor agonists. Also provided are methods for weight management, inducing satiety, and decreasing food intake, and for preventing and treating obesity, antipsychotic-induced weight gain, type 2 diabetes, Prader-Willi syndrome, tobacco/nicotine dependence, drug addiction, alcohol addiction, pathological gambling, reward deficiency syndrome, and sex addiction), obsessive-compulsive spectrum disorders and impulse control disorders (including nail-biting and onychophagia), sleep disorders (including insomnia, fragmented sleep architecture, and disturbances of slow-wave sleep), urinary incontinence, psychiatric disorders (including schizophrenia, anorexia nervosa, and bulimia nervosa), Alzheimer disease, sexual dysfunction, erectile dysfunction, epilepsy, movement disorders (including parkinsonism and antipsychotic-induced movement disorder), hypertension, dyslipidemia, nonalcoholic fatty liver disease, obesity-related renal disease, and sleep apnea. Also provided are compositions comprising a selective 5-HT2C receptor agonist, optionally in combination with a supplemental agent, and methods for reducing the frequency of smoking tobacco in an individual attempting to reduce frequency of smoking tobacco; aiding in the cessation or lessening of use of a tobacco product in an individual attempting to cease or lessen use of a tobacco product; aiding in smoking cessation and preventing associated weight gain; controlling weight gain associated with smoking cessation by an individual attempting to cease smoking tobacco; reducing weight gain associated with smoking cessation by an individual attempting to cease smoking tobacco; treating nicotine dependency, addiction and/or withdrawal in an individual attempting to treat nicotine dependency, addiction and/or withdrawal; or reducing the likelihood of relapse use of nicotine by an individual attempting to cease nicotine use comprising administering a selective 5-HT2C receptor agonist, optionally in combination with a supplemental agent.
    提供了5-HT2C受体激动剂。还提供了用于体重管理、诱导饱腹感、减少食物摄入量、预防和治疗肥胖、抗精神病药物引起的体重增加、2型糖尿病、普拉德-威利综合征、烟草/尼古丁依赖、药物成瘾、酒精成瘾、病态赌博、奖赏缺乏综合征和性成瘾)、强迫症谱系障碍和冲动控制障碍(包括咬指甲和咬甲)、睡眠障碍(包括失眠、睡眠结构碎裂和慢波睡眠紊乱)、尿失禁、精神障碍(包括精神分裂症、厌食症和暴食症)、阿尔茨海默病、性功能障碍、勃起功能障碍、癫痫、运动障碍(包括帕金森病和抗精神病药物引起的运动障碍)、高血压、血脂异常、非酒精性脂肪肝病、肥胖相关肾脏疾病和睡眠呼吸暂停。还提供了包含选择性5-HT2C受体激动剂的组合物,可选地与辅助剂结合,以及用于减少个体尝试减少吸烟频率的吸烟频率;帮助个体戒除或减少使用烟草制品的个体戒除或减少使用烟草制品;帮助戒烟并预防相关体重增加;通过个体尝试戒烟来控制与戒烟相关的体重增加;通过个体尝试戒烟来减少与戒烟相关的体重增加;治疗尼古丁依赖、成瘾和/或戒断的个体尝试治疗尼古丁依赖、成瘾和/或戒断;或减少个体尝试戒除尼古丁使用的复发可能性,包括给予选择性5-HT2C受体激动剂,可选地与辅助剂结合。
  • [EN] 5-HT2C RECEPTOR AGONISTS AND COMPOSITIONS AND METHODS OF USE<br/>[FR] AGONISTES DES RÉCEPTEURS 5-HT2C ET COMPOSITIONS ET MÉTHODES D'UTILISATION
    申请人:ARENA PHARM INC
    公开号:WO2016176177A1
    公开(公告)日:2016-11-03
    Provided in some embodiments are compounds herein. Also provided in some embodiments are methods for weight management, inducing satiety, and decreasing food intake, and for preventing and treating obesity, antipsychotic-induced weight gain, type 2 diabetes, Prader-Willi syndrome, tobacco/nicotine dependence, drug addiction, alcohol addiction, pathological gambling, reward deficiency syndrome, and sex addiction), obsessive-compulsive spectrum disorders and impulse control disorders (including nail-biting and onychophagia), sleep disorders (including insomnia, fragmented sleep architecture, and disturbances of slow-wave sleep), urinary incontinence, psychiatric disorders (including schizophrenia, anorexia nervosa, and bulimia nervosa), Alzheimer disease, sexual dysfunction, erectile dysfunction, epilepsy, movement disorders (including parkinsonism and antipsychotic-induced movement disorder), hypertension, dyslipidemia, nonalcoholic fatty liver disease, obesity-related renal disease, and sleep apnea. Also provided in some embodiments are compositions comprising a compound herein, optionally in combination with a supplemental agent, and methods for reducing the frequency of smoking tobacco in an individual attempting to reduce frequency of smoking tobacco; aiding in the cessation or lessening of use of a tobacco product in an individual attempting to cease or lessen use of a tobacco product; aiding in smoking cessation and preventing associated weight gain; controlling weight gain associated with smoking cessation by an individual attempting to cease smoking tobacco; reducing weight gain associated with smoking cessation by an individual attempting to cease smoking tobacco; treating nicotine dependency, addiction and/or withdrawal in an individual attempting to treat nicotine dependency, addiction and/or withdrawal; or reducing the likelihood of relapse use of nicotine by an individual attempting to cease nicotine use comprising administering a compound herein, optionally in combination with a supplemental agent.
    在某些实施例中提供了本文中的化合物。在某些实施例中还提供了用于体重管理、诱发饱腹感、减少食物摄入、预防和治疗肥胖、抗精神病药物引起的体重增加、2型糖尿病、普拉德-威利综合征、烟草/尼古丁依赖、药物成瘾、酒精成瘾、病理赌博、奖赏缺乏综合征、性成瘾)、强迫症谱系障碍和冲动控制障碍(包括咬指甲和咬甲)、睡眠障碍(包括失眠、睡眠结构紊乱和慢波睡眠障碍)、尿失禁、精神障碍(包括精神分裂症、厌食症和暴食症)、阿尔茨海默病、性功能障碍、勃起功能障碍、癫痫、运动障碍(包括帕金森病和抗精神病药物引起的运动障碍)、高血压、血脂异常、非酒精性脂肪肝病、肥胖相关肾脏疾病和睡眠呼吸暂停。在某些实施例中还提供了包含本文中的化合物的组合物,可选择地与辅助剂结合,并且提供了用于减少个体尝试减少吸烟频率的吸烟频率;帮助个体戒除或减少吸烟产品的使用;帮助戒烟并预防相关体重增加;通过个体试图戒烟来控制与戒烟相关的体重增加;通过个体试图戒烟来减少与戒烟相关的体重增加;治疗个体试图治疗尼古丁依赖、成瘾和/或戒断的尼古丁依赖、成瘾和/或戒断;或减少个体试图停止尼古丁使用的复发尼古丁使用的可能性,包括给予本文中的化合物,可选择地与辅助剂结合。
  • USE OF AMITIFADINE, (+)-1-(3,4-DICHLOROPHENYL)-3-AZABICYCLO[3.1.0]HEXANE IN METHODS AND COMPOSITIONS WITH ENHANCED EFFICACY AND REDUCED METABOLIC SIDE EFFECTS AND TOXICITY FOR TREATMENT OF DEPRESSION AND OTHER CENTRAL NERVOUS SYSTEM DISORDERS AND CONDITIONS AFFECTED BY MONOAMINE NEUROTRANSMITTERS
    申请人:McKinney Anthony Alexander
    公开号:US20160346249A1
    公开(公告)日:2016-12-01
    The present invention relates to (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane and pharmaceutically acceptable active salts, polymorphs, glycosylated derivatives, metabolites, solvates, hydrates, and/or prodrugs of (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane and their use alone or in combination with additional psychotherapeutic compositions in the treatment of conditions affected by monoamine neurotransmitters, including treatment of refractory individuals. (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane compositions are metabolized by either or both MAO-A or cytochrome P450 enzymes and thus are effective in the treatment of individuals with cytochrome P450 polymorphisms or who are taking other medications that affect the cytochrome P450 pathway.
    本发明涉及(+)-1-(3,4-二氯苯基)-3-氮杂双环[3.1.0]己烷及其药用可接受的活性盐、多晶形态、糖基化衍生物、代谢物、溶剂合物、水合物和/或前药,以及其单独使用或与额外的精神疗法组合一起治疗受单胺神经递质影响的疾病,包括难治性个体的治疗。 (+)-1-(3,4-二氯苯基)-3-氮杂双环[3.1.0]己烷组合物被MAO-A或细胞色素P450酶中的任一或两者代谢,因此对患有细胞色素P450多态性或正在服用影响细胞色素P450途径的其他药物的个体进行治疗是有效的。
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