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TBS-noribogaine | 1538614-01-5

中文名称
——
中文别名
——
英文名称
TBS-noribogaine
英文别名
——
TBS-noribogaine化学式
CAS
1538614-01-5
化学式
C25H38N2OSi
mdl
——
分子量
410.675
InChiKey
NKALUDMOIKARBK-FSXUSMNQSA-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):
    6.31
  • 重原子数:
    29.0
  • 可旋转键数:
    3.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.68
  • 拓扑面积:
    28.26
  • 氢给体数:
    1.0
  • 氢受体数:
    2.0

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    TBS-noribogaine盐酸 、 palladium 10% on activated carbon 、 氢气sodium hexamethyldisilazane 作用下, 以 四氢呋喃1,4-二氧六环甲醇乙酸乙酯 为溶剂, -78.0~20.0 ℃ 、101.33 kPa 条件下, 反应 48.33h, 生成
    参考文献:
    名称:
    Compositions comprising noribogaine and an excipient to facilitate transport across the blood brain barrier
    摘要:
    这项发明通常涉及包含诺利波甲碱和辅助剂以促进穿越血脑屏障的组合物。
    公开号:
    US08637648B1
  • 作为产物:
    描述:
    10-ethoxyibogamine 在 N,N-二异丙基乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 TBS-noribogaine
    参考文献:
    名称:
    [EN] IBOGAINE ANALOGS AS THERAPEUTICS FOR NEUROLOGICAL AND PSYCHIATRIC DISORDERS
    [FR] ANALOGUES DE L'IBOGAÏNE EN TANT QU'AGENTS THÉRAPEUTIQUES POUR DES TROUBLES NEUROLOGIQUES ET PSYCHIATRIQUES
    摘要:
    The present invention provides a compound having the structure: formula wherein X1 is H or alkyl; Y1 is H, -alkyl, -alkenyl, -alkynyl, alkylaryl, -cycloalkyl, - aryl, heteroaryl, -alkyl-Y3 or -alkyl-C(O)Y4, and Y2 is H, -alkyl, -alkenyl, -alkynyl, alkylaryl, -cycloalkyl, - aryl, heteroaryl, -alkyl-Yg or -alkyl-C(O)Y4, wherein each Y3 is, independently, -OH, -O(alkyl), -NH2, - NH(alkyl) or halogen, and each Y4 is, independently, -OH, -O(alkyl), -NH2, -NH(alkyl) or -N(alkyl)2; Z1 is H, -alkyl, -alkenyl, -alkynyl, alkylaryl, -aryl, heteroaryl, -alkyl-Zg or -alkyl-C(O)Z4, and Z2 is H, -alkyl, -alkenyl, -alkynyl, alkylaryl, -aryl, heteroaryl, -alkyl-Zg or -alkyl-C(O)Z4, wherein each Z3 is, independently, -OH, -O(alkyl), -NH2, - NH(alkyl) or halogen, and each Z4 is, independently, -OH, -O(alkyl), -NH2, -NH(alkyl) or -N(alkyl)2; R1, R2, R3 and R4 are each, independently, -H, -F, -Cl, -Br, -I, -NO2, -CN, -CF3, -CF2H, -OCF3, -(alkyl), -(alkenyl), -(alkynyl), -(aryl), -(heteroaryl), -OH, -OAc, -O-(alkyl), -O-(alkenyl), - O-(alkynyl), -O-(aryl), -O-(heteroaryl), -SH, -S-(alkyl), S (alkenyl), -S-(alkynyl), -S-(aryl), -S-(heteroaryl), -NH2, -NH- (alkyl), -NH-(alkenyl), -NH-(alkynyl), -NH-(aryl), -NH- (heteroaryl), -C(0)R5, -S(O)R5, -SO2R5, -NHSO2R5, -0C(0)R5, SC(0)R5, -NHC(O)R6 or -NHC(S)R6, wherein each R5 is, independently, -(alkyl), -(aryl), (heteroaryl), -OH, -O(alkyl), -NH2, -NH(alkyl) or N(alkyl)2, and wherein each R6 is, independently, -(alkyl), -(aryl), -O- (alkyl), -S-(alkyl), -S-(aryl), -NH2, -NH(alkyl) or N(alkyl)2, wherein the compound is other than any of ibogaine, ibogamine, N- methyl-ibogaine, N-methyl-noribogaine, N-ethyl-noribogaine, N-methyl- ibogamine or 10-ethoxy-ibogamine, or a pharmaceutically acceptable salt of the compound, and methods of using the composition to treat pain, depressive disorders, mood disorders, anxiety disorders, substance use disorders, opioid use disorders, and opioid withdrawal symptoms.
    公开号:
    WO2022020352A1
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文献信息

  • N-substituted noribogaine prodrugs
    申请人:Mash Deborah C.
    公开号:US08741891B1
    公开(公告)日:2014-06-03
    This invention relates generally to prodrugs of noribogaine. This invention also relates to pharmaceutical compositions comprising the prodrugs of noribogaine as well as method of treating pain, addiction and/or stress using such compounds and/or pharmaceutical compositions.
    这项发明通常涉及诺利波甲醇的前药。该发明还涉及包含诺利波甲醇前药的药物组合物,以及使用这些化合物和/或药物组合物治疗疼痛、成瘾和/或压力的方法。
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同类化合物

马山茶碱 非洲伏康树碱 长春质碱 老刺木胺 老刺木任 硫酸长春质碱 海尼山辣椒碱羟基假吲哚 榴花碱 柳黄酸 伏康京碱 伊菠胺-18-羧酸甲酯 伊菠胺 伊菠加因盐酸盐 伊博格碱 7-羟基-1-去氢老刺木碱 20-羟基榴花碱 14-((3alpha)-17-甲氧基-17-氧代派利文碱-3-基)-伊菠胺-18-羧酸甲酯 13-甲氧基-14-[(3A)-17-甲氧基-17-氧代派利文碱-3-基]-伊菠胺-18-羧酸甲酯 13-甲氧基-12-[(3a)-17-甲氧基-17-氧代派利文碱-3-基]-伊菠胺-18-羧酸甲酯 12-((3alpha)-17-甲氧基-17-氧代派利文碱-3-基)-伊菠胺-18-羧酸甲酯 11-羟基狗牙花定 10-羟基狗牙花定 (4a,20S)-20-羟基伊菠胺-18-羧酸甲酯 (2S)-1,2,3,4,4abeta,5,6,7,7a,12bbeta-十氢-4alpha-(1-羟基乙基)-9-甲氧基-2alpha,5alpha-甲桥吲哚并[3,2-d][1]苯并氮杂卓-7alpha-醇 4,20-Dehydrovoacangin 17a,17a,18-trideuterio-12,13-dimethoxy-17a-homo-ibogamine Conodiparine A Hydroxyindolenin von Coronaridin (+/-)-(phenylsulfonyl)50nor-15-oxocoronaridine methyl (6R,6aS,7S,8R,9S)-8-acetoxy-7-ethyl-13a-hydroxy-6a,7,9,10,13,13a-hexahydro-8H-6,9-methanopyrido[1',2':1,2]azepino[4,5-b]indole-6(12H)-carboxylate 20-epi-15-oxocoronaridine 15-S-methylcatharanthine 15β-(tosyloxy)coronaridine N-demethylvoacamine Voacanginol-19,19,22,22-d(4) noribogaine phosphate Isovoacangin-19-d(1) noribogaine sulfate (6R,6aS,7S,9R)-2-((tert-butyldimethylsilyl)oxy)-N-(2-(dimethylamino)ethyl)-7-ethyl-6,6a,7,8,9,10,12,13-octahydro-5H-6,9-methanopyrido[1',2':1,2]azepino[4,5-b]indole-5-carboxamide Coronaridin-19-d(1) 13-(4-acetyl-16-methoxycarbonyl-17,22-dinor-vobasan-3-yl)-12-methoxy-ibogamine-18-carboxylic acid methyl ester Dihydrocatharanthinol-O-mesylat 2-Methoxyethyl 21-methoxyibogamine-18-carboxylate 7-ethyl-6-(toluene-4-sulfonyloxymethyl)-6,6a,7,8,9,10,12,13-octahydro-5H-6,9-methano-pyrido[1',2':1,2]azepino[4,5-b]indole Isovoacangin-12,14,19-d(3) dideuterio-(12,13-dimethoxy-ibogamin-18-yl)-methanol