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(R)-6-bromo-8-fluoro-4-methyl-3,4-dihydro-2H-pyrazino[1,2-a]indol-1-one | 396076-62-3

中文名称
——
中文别名
——
英文名称
(R)-6-bromo-8-fluoro-4-methyl-3,4-dihydro-2H-pyrazino[1,2-a]indol-1-one
英文别名
(4R)-6-bromo-8-fluoro-4-methyl-3,4-dihydro-2H-pyrazino[1,2-a]indol-1-one
(R)-6-bromo-8-fluoro-4-methyl-3,4-dihydro-2H-pyrazino[1,2-a]indol-1-one化学式
CAS
396076-62-3
化学式
C12H10BrFN2O
mdl
——
分子量
297.127
InChiKey
MHOVNONRTMDMII-ZCFIWIBFSA-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):
    2.5
  • 重原子数:
    17
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    34
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Piperazine derivatives
    申请人:——
    公开号:US20020169163A1
    公开(公告)日:2002-11-14
    Piperazine derivatives, as well as pharmaceutically acceptable salts, solvates and esters thereof, can be used in the form of pharmaceutical preparations for the treatment or prevention of disorders of the central nervous system, damage to the central nervous system, cardiovascular disorders, gastrointestinal disorders, diabetes insipidus, type II diabetes, obesity and sleep apnoea.
    哌嗪生物以及其中医药可接受的盐、溶剂合物和酯,可用于制药制剂的形式,用于治疗或预防中枢神经系统疾病、中枢神经系统损伤、心血管疾病、胃肠疾病、尿崩症、2型糖尿病、肥胖和睡眠呼吸暂停。
  • [EN] PIPERAZINO[1,2-A]INDOL-1-ONES AND [1,4]DIAZEPINO[1,2-A]INDOL-1-ONE<br/>[FR] PIPÉRAZINO[1,2-A]INDOL-1-ONES ET [1,4]DIAZÉPINO[1,2-A]INDOL-1-ONE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2014023674A1
    公开(公告)日:2014-02-13
    The present invention relates to compounds of general formula (I), wherein R1 is hydrogen, halogen, lower alkyl, lower alkoxy, lower alkoxy substituted by halogen or cyano; R2 is hydrogen, lower alkyl or lower alkyl substituted by halogen; R3 is phenyl, benzo[1,3]dioxolyl, 2,3-dihydro-benzofuran-5-yl or a 5- and 6-membered heteroaryl, wherein phenyl and the 5- and 6-membered heteroaryl groups may be substituted by one or more substituents, selected from cyano, nitro, amino and lower di-alkylamino, lower alkyl sulfonyl, lower alkoxy, lower alkoxy substituted by halogen, halogen, lower alkyl, lower alkyl substituted by halogen or lower alkyl substituted by hydroxyl; X is -CH(lower alkyl)-, -CH2-, -CH2CH2- or –CH(lower alkyl)CH2-; R is hydrogen or lower alkyl; n is 1 or 2; or to a pharmaceutically acceptable acid addition salt, to a racemic mixture or to its corresponding enantiomer and/or optical isomers thereof. The compounds may be used for the treatment of schizophrenia, obsessive-compulsive personality disorder, major depression, bipolar disorders, anxiety disorders, normal aging, epilepsy, retinal degeneration, traumatic brain injury, spinal cord injury, post-traumatic stress disorder, panic disorder, Parkinson's disease, dementia, Alzheimer's disease, mild cognitive impairment, chemotherapy-induced cognitive dysfunction, Down syndrome, autism spectrum disorders, hearing loss, tinnitus, spinocerebellar ataxia, amyotrophic lateral sclerosis, multiple sclerosis, Huntington's disease, stroke, radiation therapy, chronic stress, abuse of neuro-active drugs, such as alcohol, opiates, methamphetamine, phencyclidine and cocaine.
    本发明涉及一般式(I)的化合物,其中R1是氢、卤素、较低烷基、较低烷氧基、被卤素或基取代的较低烷氧基;R2是氢、较低烷基或被卤素取代的较低烷基;R3是苯基、苯并[1,3]二噁英基、2,3-二氢-苯并呋喃-5-基或5-和6-成员杂芳基,其中苯基和5-和6-成员杂芳基可能被基、硝基、基和较低二烷基基、较低烷基磺酰基、较低烷氧基、被卤素取代的较低烷氧基、卤素、较低烷基、被卤素取代的较低烷基或被羟基取代的较低烷基等一个或多个取代基取代;X是-CH(较低烷基)-、-CH2-、- -或-CH(较低烷基) -;R是氢或较低烷基;n是1或2;或是药学上可接受的酸盐,或是外消旋混合物,或是其对映体和/或光学异构体。这些化合物可用于治疗精神分裂症、强迫性人格障碍、重度抑郁症、躁郁症、焦虑障碍、正常衰老、癫痫、视网膜退化、创伤性脑损伤、脊髓损伤、创伤后应激障碍、惊恐障碍、帕森病、痴呆症、阿尔茨海默病、轻度认知障碍、化疗诱导的认知功能障碍、唐氏综合征、自闭症谱系障碍、听力丧失、耳鸣、脊髓小脑共济失调、肌萎缩性侧索硬化、多发性硬化、亨廷顿病、中风、放射治疗、慢性压力、对神经活性药物的滥用,如酒精、阿片类药物、甲基苯丙胺、芬西克林和可卡因
  • [EN] PIPERAZINE DERIVATIVES<br/>[FR] DERIVES DE LA PIPERAZINE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2002010169A1
    公开(公告)日:2002-02-07
    The present invention refers to chemical compounds of formula (I) as well as pharmaceutically usable salts, solvates and esters thereof, wherein R1 to R8 have the significance given in claim 1. They can be used in the form of pharmaceutical preparations for the treatment or prevention of disorders of the central nervous system, damage to the central nervous system, cardiovascular disorders, gastrointestinal disorders, diabetes insipidus, obesity and sleep apnoea.
    本发明涉及化学式(I)的化合物,以及其可用于制药的盐,溶剂合物和酯,其中R1至R8具有权利要求1中给出的意义。它们可以用于制药制剂的形式,用于治疗或预防中枢神经系统的疾病,中枢神经系统的损伤,心血管疾病,胃肠疾病,尿崩症,肥胖症和睡眠呼吸暂停。
  • Anti-obesity 1,2,3,4,10,10a-hexahydropyrazino[1,2-a] indoles
    申请人:Bentley Mark Jonathan
    公开号:US20050239789A1
    公开(公告)日:2005-10-27
    The present invention is directed to 1,2,3,4,10,10a,-hexahydropyrazino[1,2-a]indole derivatives as well as pharmaceutically acceptable salts, solvates and esters thereof, wherein R 1 to R 8 have the significance given in claim 1 be used in the form of pharmaceutical preparations for the treatment or prevention of disorders of the central nervous system, damage to the central nervous system, cardiovascular disorders, gastrointestinal disorders, diabetes insipidus, obesity and sleep apnea.
    本发明涉及1,2,3,4,10,10a,-六氢吡嗪并[1,2-a]吲哚生物,以及其药学上可接受的盐、溶剂和酯,其中R1至R8在权利要求书中所给出的意义下使用,用于制备药物制剂,用于治疗或预防中枢神经系统疾病、中枢神经系统损伤、心血管疾病、胃肠道疾病、尿崩症、肥胖症和睡眠呼吸暂停。
  • Anti-obesity 1, 2, 3, 4, 10, 10a-hexahydropyrazino[1, 2-a] indoles
    申请人:——
    公开号:US20030216401A1
    公开(公告)日:2003-11-20
    The present invention is directed to 1,2,3,4,10,10a,-hexahydro-pyrazino[1,2-a]indole derivatives as well as pharmaceutically acceptable salts, solvates and esters thereof, wherein R 1 to R 8 have the significance given in claim 1 be used in the form of pharmaceutical preparations for the treatment or prevention of disorders of the central nervous system, damage to the central nervous system, cardiovascular disorders, gastrointestinal disorders, diabetes insipidus, obesity and sleep apnea.
    本发明涉及1,2,3,4,10,10a,-六氢吡嗪[1,2-a]吲哚生物以及药学上可接受的盐、溶剂和酯,其中R1到R8具有权利要求1中所给定的含义,以药物制剂的形式用于治疗或预防中枢神经系统疾病、中枢神经系统损伤、心血管疾病、胃肠道疾病、尿崩症、肥胖症和睡眠呼吸暂停。
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