摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2,3-dihydro-9H-1,4-dioxino[2,3-g]indole | 327183-56-2

中文名称
——
中文别名
——
英文名称
2,3-dihydro-9H-1,4-dioxino[2,3-g]indole
英文别名
3,9-dihydro-2H-[1,4]dioxino[2,3-g]indole
2,3-dihydro-9H-1,4-dioxino[2,3-g]indole化学式
CAS
327183-56-2
化学式
C10H9NO2
mdl
——
分子量
175.187
InChiKey
CDUQBYPFLOLTML-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):
    1.8
  • 重原子数:
    13
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    34.2
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • Condensed indoline derivatives and their use as 5HT, in particular 5HT2c, receptor ligands
    申请人:Roffey Richard Anthony Jonathan
    公开号:US20050187282A1
    公开(公告)日:2005-08-25
    A chemical compound of formula (I) wherein R 1 and R 2 are independently selected from hydrogen and alkyl; R 3 is alkyl; R 4 and R 5 are selected from hydrogen and alkyl; R 6 and R 7 are independently selected from hydrogen, halogen, hydroxyl, alkyl, aryl, amino, alkylamino, dialkylamino, alkoxy, aryloxy, alkylthio, alkylsulfoxyl, nitro, carbonitrile, carbo-alkoxy, carbo-aryloxy and carboxyl; and A is a 5- or 6-membered ring optionally containing one or more heteroatoms wherein the atoms of the ring A, other than the unsaturated carbon atoms of the phenyl ring to which the ring A is fused, are saturated or unsaturated, and pharmaceutically acceptable salts, addition compounds and prodrugs thereof; and the use thereof in therapy, particularly as an agonist or antagonist of a 5HT receptor, particularly a 5HT 2C receptor, for instance in the treatment of disorders of the central nervous system; damage to the central nervous system; cardiovascular disorders; gastrointestinal disorders; diabetes insipidus, and sleep apnea, and particularly for the treatment of obesity.
    化学式(I)的化合物,其中R1和R2分别选自氢和烷基;R3是烷基;R4和R5选自氢和烷基;R6和R7分别选自氢、卤素、羟基、烷基、芳基、基、烷基基、二烷基基、烷氧基、芳氧基、烷基基、烷基亚砜基、硝基、基、羧酸酯基、羧酸芳酯基和羧基;A是一个含有一个或多个杂原子的5-或6元环,其中环A的原子除了与环A融合的苯环的不饱和碳原子外,可以是饱和的或不饱和的,以及其药学上可接受的盐、加合物和前药;以及其在治疗中的用途,特别是作为5HT受体的激动剂或拮抗剂,特别是5HT2C受体,例如在治疗中枢神经系统疾病;中枢神经系统损伤;心血管疾病;胃肠道疾病;尿崩症和睡眠呼吸暂停症,特别是用于肥胖症的治疗。
  • Condensed indoline derivatives and their use as 5HT, in particular 5HT2C, receptor ligands
    申请人:Roffey Richard Anthony Jonathan
    公开号:US20050192334A1
    公开(公告)日:2005-09-01
    A chemical compound of formula (I) wherein R 1 and R 2 are independently selected from hydrogen and alkyl; R 3 is alkyl; R 4 and R 5 are selected from hydrogen and alkyl; R 6 and R 7 are independently selected from hydrogen, halogen, hydroxyl, alkyl, aryl, amino, alkylamino, dialkylamino, alkoxy, aryloxy, alkylthio, alkylsulfoxyl, nitro, carbonitrile, carbo-alkoxy, carbo-aryloxy and carboxyl; and A is a 5- or 6-membered ring optionally containing one or more heteroatoms wherein the atoms of the ring A, other than the unsaturated carbon atoms of the phenyl ring to which the ring A is fused, are saturated or unsaturated, and pharmaceutically acceptable salts, addition compounds and prodrugs thereof; and the use thereof in therapy, particularly as an agonist or antagonist of a 5HT receptor, particularly a 5HT 2C receptor, for instance in the treatment of disorders of the central nervous system; damage to the central nervous system; cardiovascular disorders; gastrointestinal disorders; diabetes insipidus, and sleep apnea, and particularly for the treatment of obesity.
    化学式为(I)的化合物,其中R1和R2独立地选自氢和烷基;R3为烷基;R4和R5选自氢和烷基;R6和R7独立地选自氢、卤素、羟基、烷基、芳基、基、烷基基、二烷基基、烷氧基、芳氧基、烷基、烷基亚砜基、硝基、基、羧基酯基、芳羧基酯基和羧基;A是一个5-或6-成员环,可选地含有一个或多个杂原子,其中环A的原子除与环A融合的苯环的不饱和碳原子外,均为饱和或不饱和的,以及其药学上可接受的盐、加合物和前药;以及其在治疗中的使用,特别是作为5HT受体的激动剂或拮抗剂,特别是5HT2C受体,例如在中枢神经系统疾病、中枢神经系统损伤、心血管疾病、胃肠道疾病、尿崩症和睡眠呼吸暂停症的治疗中,特别是用于肥胖症的治疗。
  • Condensed indoline derivatives and their use as 5HT , in particular 5hHT2c, receptor ligands
    申请人:Roffey Anthony Jonathan Richard
    公开号:US20070105889A1
    公开(公告)日:2007-05-10
    A chemical compound of formula (I) wherein R 1 and R 2 are independently selected from hydrogen and alkyl; R 3 is alkyl; R 4 and R 5 are selected from hydrogen and alkyl; R 6 and R 7 are independently selected from hydrogen, halogen, hydroxyl, alkyl, aryl, amino, alkylamino, dialkylamino, alkoxy, aryloxy, alkylthio, alkylsulfoxyl, nitro, carbonitrile, carbo-alkoxy, carbo-aryloxy and carboxyl; and A is a 5- or 6-membered ring optionally containing one or more heteroatoms wherein the atoms of the ring A, other than the unsaturated carbon atoms of the phenyl ring to which the ring A is fused, are saturated or unsaturated, and pharmaceutically acceptable salts, addition compounds and prodrugs thereof; and the use thereof in therapy, particularly as an agonist or antagonist of a 5HT receptor, particularly a 5HT 2C receptor, for instance in the treatment of disorders of the central nervous system; damage to the central nervous system; cardiovascular disorders; gastrointestinal disorders; diabetes insipidus, and sleep apnea, and particularly for the treatment of obesity.
    化学式为(I)的化合物,其中R1和R2分别选自氢和烷基;R3为烷基;R4和R5选自氢和烷基;R6和R7分别选自氢、卤素、羟基、烷基、芳基、基、烷基基、二烷基基、烷氧基、芳氧基、烷基、烷基亚砜基、硝基、基、羧甲氧基、羧芳氧基和羧基;A是一个5或6元环,可以包含一个或多个杂原子,环A的原子,除了与环A融合的苯环的不饱和碳原子外,都是饱和或不饱和的,并且其药物可接受的盐、加成物和前药;以及其在治疗中的应用,特别是作为5HT受体的激动剂或拮抗剂,特别是5HT2C受体,例如在中枢神经系统疾病的治疗中;中枢神经系统损伤;心血管疾病;胃肠道疾病;尿崩症和睡眠呼吸暂停症,特别是用于肥胖症的治疗。
  • Condensed indoline derivatives and their use as 5HT, in particular 5HT2C, Receptor ligands
    申请人:Roffey Jonathan Richard Anthony
    公开号:US20080125455A1
    公开(公告)日:2008-05-29
    A chemical compound of formula (I) wherein R 1 and R 2 are independently selected from hydrogen and alkyl; R 3 is alkyl; R 4 and R 5 are selected from hydrogen and alkyl; R 6 and R 7 are independently selected from hydrogen, halogen, hydroxyl, alkyl, aryl, amino, alkylamino, dialkylamino, alkoxy, aryloxy, alkylthio, alkylsulfoxyl, nitro, carbonitrile, carbo-alkoxy, carbo-aryloxy and carboxyl; and A is a 5- or 6-membered ring optionally containing one or more heteroatoms wherein the atoms of the ring A, other than the unsaturated carbon atoms of the phenyl ring to which the ring A is fused, are saturated or unsaturated, and pharmaceutically acceptable salts, addition compounds and prodrugs thereof; and the use thereof in therapy, particularly as an agonist or antagonist of a 5HT receptor, particularly a 5HT 2C receptor, for instance in the treatment of disorders of the central nervous system; damage to the central nervous system, cardiovascular disorders; gastrointestinal disorders; diabetes insipidus, and sleep apnea, and particularly for the treatment of obesity.
    化学式为(I)的化合物,其中R1和R2独立地选自氢和烷基;R3是烷基;R4和R5选自氢和烷基;R6和R7独立地选自氢、卤素、羟基、烷基、芳基、基、烷基基、二烷基基、烷氧基、芳氧基、烷基、烷基亚砜基、硝基、基、羧甲氧基、羧芳氧基和羧基;A是一个5或6成员环,可选地含有一个或多个杂原子,其中环A的原子,除了与环A融合的苯环的不饱和碳原子外,均为饱和或不饱和的,并且其药学上可接受的盐、加合物和前药;以及在治疗中的使用,特别是作为5HT受体的激动剂或拮抗剂,特别是5HT2C受体,例如用于治疗中枢神经系统疾病;中枢神经系统损伤、心血管疾病;胃肠道疾病;尿崩症和睡眠呼吸暂停症,特别是用于治疗肥胖症。
  • CONDENSED INDOLINE DERIVATIVES AND THEIR USE AS 5HT, IN PARTICULAR 5HT2C, RECEPTOR LIGANDS
    申请人:VERNALIS RESEARCH LIMITED
    公开号:EP1202964B1
    公开(公告)日:2005-10-12
查看更多

同类化合物

顺式-6-氯-4-甲基-4-苯基-4H-1,3-苯并二氧杂环己-2-羧酸 阿莫齐特 苯并二氧六环-6-甲酸甲酯 苯并二氧六环-6-甲酰胺 苯并二氧六环-5-甲酸甲酯 苯并二氧六环-5-甲酰胺 苯并二氧六环-2-磺酰氯 苯并-1,4-二氧六环-6-硼酸 艾泽罗西 脲,N-(4-甲基-1-哌嗪基)- 胍苯克生 胍美柳 胍生 羧基-6-苯并(4H)二恶英-1,3 美商陆酚A 维兰特罗杂质4 硫酸(2:1)(1,4-苯并二噁烷-6-基甲基)胍正离子 盐酸艾美洛沙 盐酸哌罗克生 盐酸[(7-溴-2,3-二氢-1,4-苯并二恶英-6-基)甲基]肼 甲基氨基甲酸1,4-苯并二恶烷-5-基酯 甲基8-甲基-2,3-二氢-1,4-苯并二氧杂环己烷-6-羧酸酯 甲基7-甲基-2,3-二氢-1,4-苯并二氧杂环己烷-5-羧酸酯 甲基4-[(1E)-3-乙基-3-(羟甲基)三氮杂-1-烯-1-基]苯酸酯 甲基-[2-[(7-丙-2-烯基-2,3-二氢-1,4-苯并二氧杂环己-8-基)氧基]乙基]氯化铵 甲基(2S,4R)-6-氯-4-甲基-4-(2-噻吩基)-4H-1,3-苯并二氧杂环己烷-2-羧酸酯 溴(2,3-二氢-1,4-苯并二氧杂环己-6-基)镁 沙丁胺醇缩丙酮 异美商陆素 A 异戊苯恶烷 度莫辛 布他莫生 安必罗山 地奥地洛 噻唑并[5,4-b]吡啶-2-胺,N-[[1-[(2,3-二氢-1,4-苯并二噁英-2-基)甲基]-4-哌啶基]甲基]- 哌扑罗生 咪洛克生 咪唑克生盐酸盐 吡啶-3-磺酰氯盐酸盐 叔丁基 (2,3-二氢苯并[b][1,4]二噁英-6-基)氨基甲酸酯 反式-2,3-二氢-N-((4-(2-苯氧基乙基)-1-哌嗪基)甲基)-1,4-苯并二氧六环-2-甲酰胺 双恶哌嗪 冰达卡醇 依利格鲁司特酒石酸盐 依利格鲁司特杂质 依利格鲁司特中间体5 依利格鲁司特 亚达唑散 二氨基亚甲基-(2,3-二氢-1,4-苯并二氧杂环己-2-基甲基)铵硫酸盐 二-(叔丁基)2-(2,2-二甲基-4H-1,3-苯并二恶英-6-基)-2-氧代乙基亚氨基二碳酸