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3-formyl-2-methoxy-5,6-dichloro-1-(β-D-ribofuranosyl)indole

中文名称
——
中文别名
——
英文名称
3-formyl-2-methoxy-5,6-dichloro-1-(β-D-ribofuranosyl)indole
英文别名
5,6-dichloro-2-methoxy-3-formyl-1-(β-D-ribofuranosyl)indole;5,6-dichloro-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-2-methoxy-indole-3-carbaldehyde;5,6-dichloro-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-methoxyindole-3-carbaldehyde
3-formyl-2-methoxy-5,6-dichloro-1-(β-D-ribofuranosyl)indole化学式
CAS
——
化学式
C15H15Cl2NO6
mdl
——
分子量
376.193
InChiKey
IUOAPFCKYAOYBB-RGCMKSIDSA-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):
    1.4
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    101
  • 氢给体数:
    3
  • 氢受体数:
    6

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

反应信息

  • 作为产物:
    描述:
    sodium methylate2,5,6-trichloro-3-formyl-1-(5-O-acetyl-β-D-ribofuranosyl)indole碳酸氢钠 作用下, 以 甲醇 为溶剂, 反应 0.5h, 以42%的产率得到3-formyl-2-methoxy-5,6-dichloro-1-(β-D-ribofuranosyl)indole
    参考文献:
    名称:
    [EN] INDOLE ANTIVIRAL COMPOSITIONS AND METHODS
    [FR] COMPOSITIONS ANTIVIRALES A BASE D'INDOLE ET PROCEDES CORRESPONDANTS
    摘要:
    本发明提供了新颖的化合物和它们的使用方法。具体来说,本发明提供了吲哚衍生物(例如如公式(I)所示)和相关化合物,以及使用吲哚衍生物和相关化合物作为治疗剂治疗多种疾病的方法,包括与病毒感染和心血管疾病相关的疾病。
    公开号:
    WO2005034943A1
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文献信息

  • Indole antiviral compositions and methods
    申请人:Townsend B. Leroy
    公开号:US20050143329A1
    公开(公告)日:2005-06-30
    The present invention provides novel chemical compounds, and methods for their use. In particular, the present invention provides indole derivatives (e.g. as shown in Formula (I)) and related compounds and methods of using indole derivatives and related compounds as therapeutic agents to treat a number of conditions, including those associated with viral infection and cardiovascular diseases.
    本发明提供了新的化合物和其使用方法。特别地,本发明提供吲哚衍生物(例如如式(I)所示)和相关化合物以及使用吲哚衍生物和相关化合物作为治疗剂治疗多种疾病的方法,包括与病毒感染和心血管疾病有关的疾病。
  • Indole Antiviral Compositions And Methods
    申请人:Townsend Leroy B.
    公开号:US20090281052A1
    公开(公告)日:2009-11-12
    The present invention provides novel chemical compounds, and methods for their use. In particular, the present invention provides indole derivatives (e.g. as shown in Formula (I)) and related compounds and methods of using indole derivatives and related compounds as therapeutic agents to treat a number of conditions, including those associated with viral infection and cardiovascular diseases.
    本发明提供了新型化合物及其使用方法。具体来说,本发明提供吲哚衍生物(例如如式(I)所示)和相关化合物,以及使用吲哚衍生物和相关化合物作为治疗剂治疗多种疾病的方法,包括与病毒感染和心血管疾病相关的疾病。
  • Synthesis and Antiviral Activity of Some 2-Substituted 3-Formyl-and 3-Cyano-5,6-Dichloroindole Nucleosides
    作者:John D. Williams、John C. Drach、Leroy B. Townsend
    DOI:10.1080/15257770500265836
    日期:2005.9.1
    A series of dichlorinated indole nucleosides has been synthesized and tested for activity against human cytomegalovirus (HCMV) and herpes simplex virus type-1 (HSV-1) and for cytotoxicity. The isopropylidene-protected analogs of the previously reported 3-formyl-2,5,6-trichloro-1-(beta-D-ribofuranosyl)indole (FTCRI) and 3-cyano-2,5,6-trichloro-1-(beta-D-ribofuranosyl)indole (CTCRI) were modified by nucleophilic displacement of the 2-chloro substituent using secondary amines. Deprotection of the intermediates provided 2-substituted analogs of FTCRI and CTCRI in good yield. There was a significant difference in reactivity between the isopropylidene-protected and the fully deprotected FTCRI and CTCRI with respect to nucleophilic displacement of the 2-chloro substituent using dialkylamines. This difference in reactivity was not observed with monoalkylamines or with alkoxides, and the corresponding 2-alkylamino- and 2-methoxy substituted analogs were synthesized from FTCRI and CTCRI directly. None of the synthesized analogs demonstrated potent antiviral activity without some corresponding cytotoxicity.
  • US7419963B2
    申请人:——
    公开号:US7419963B2
    公开(公告)日:2008-09-02
  • US7625871B2
    申请人:——
    公开号:US7625871B2
    公开(公告)日:2009-12-01
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同类化合物

3-formyl-2-methoxy-5,6-dichloro-1-(β-D-ribofuranosyl)indole 3-formyl-2-pyrrolidino-5,6-dichloro-1-(β-D-ribofuranosyl)indole 3-formyl-2-dimethylamino-5,6-dichloro-1-(β-D-ribofuranosyl)indole (2R,3S,4R)-2-Hydroxymethyl-5-(5-nitro-indol-1-yl)-tetrahydro-furan-3,4-diol 4,6-bis(furan-2-yl)-9-β-D-ribofuranosyl-9H-pyrimido[4,5-b]indole 6-chloro-4-(thiophen-2-yl)-9-β-D-ribofuranosyl-9H-pyrimido[4,5-b]indole 4-((furan-2-yl)-6-(furan-3-yl)-9-β-D-ribofuranosyl)-9H-pyrimido[4,5-b]indole 4-(benzofuran-2-yl)-6-chloro-9-β-D-ribofuranosyl-9H-pyrimido[4,5-b]indole 6-chloro-4-(thiophen-3-yl)-9-β-D-ribofuranosyl-9H-pyrimido[4,5-b]indole 4-((furan-2-yl)-6-phenyl-9-β-D-ribofuranosyl)-9H-pyrimido[4,5-b]indole 6-chloro-4-phenyl-β-D-ribofuranosyl-9H-pyrimido[4,5-b]indole 6-chloro-4-(furan-2-yl)-9-b-D-ribofuranosyl-9H-pyrimido[4,5-b]indole 6-chloro-4-(furan-3-yl)-9-b-D-ribofuranosyl-9H-pyrimido[4,5-b]indole 4-amino-5-butyl-9-β-D-ribofuranosylpyrimido[4,5-b]indole 1H-Indole, 6-fluoro-1-beta-D-ribofuranosyl- [4-Acetyloxy-2-(hydroxymethyl)-5-indol-1-yloxolan-3-yl] acetate 4-amino-6-benzofuran-2-yl-9-β-D-ribofuranosylpyrimido[4,5-b]indole 5,6-dichloro-2-bromo-3-formyl-1-(5-O-acetyl-β-D-ribofuranosyl)indole 2-bromo-5,6-dichloro-1-(2,3-O-isopropylidene-β-D-ribofuranosyl)indole 2-bromo-1-(5-O-tert-butyldimethylsilyl-2,3-O-isopropylidene-β-D-ribofuranosyl)-5,6-dichloroindole methyl 2,5,6-trichloro-1-(β-D-ribofuranosyl) indole-3-formimidate 4-(furan-2-yl)-9-β-D-ribofuranosyl-9H-pyrimido[4,5-b]indole 3-[1-[(2R,3R,4R,5R)-3,4-bis(phenylmethoxy)-5-(phenylmethoxymethyl)oxolan-2-yl]-6-phenylmethoxyindol-3-yl]-4-(1H-indol-3-yl)-1-methylpyrrole-2,5-dione tert-butyl 3-[4-[1-[(2R,3R,4R,5R)-3,4-bis(phenylmethoxy)-5-(phenylmethoxymethyl)oxolan-2-yl]-6-phenylmethoxyindol-3-yl]-1-methyl-2,5-dioxopyrrol-3-yl]indole-1-carboxylate 14-(β-D-ribofuranosyl)-naphtho[2,1-α]pyrrolo[3,4-c] carbazole-5,7 (6H,12H)-dione 4-amino-5-phenyl-9-β-D-ribofuranosylpyrimido[4,5-b]indole 4-amino-5-chloro-9-β-D-ribofuranosylpyrimido[4,5-b]indole 4-amino-5-thiophen-3-yl-9-β-D-ribofuranosylpyrimido[4,5-b]indole 4-Amino-6-phenyl-9-β-D-ribofuranosylpyrimido[4,5-b]indole 1-(β-D-ribofuranosyl)indol-3-acetic acid ethyl 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)indol-3-acetate methyl 1-(β-D-ribofuranosyl)indol-3-acetate 1'-deoxy-1'-(6-fluoroindolyl)-β-D-ribofuranose 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-1H-indole 1-(2'-O-methyl-β-D-ribofuranosyl)-5-nitroindole 4-amino-6-thiophen-2-yl-9-β-D-ribofuranosylpyrimido[4,5-b]indole 2,5,6-trichloro-1-(2,3-O-isopropylidene-β-D-ribofuranosyl)indole-3-carboxamide 2,5,6-trichloro-1-(2,3-O-isopropylidene-5-O-p-toluenesulfonyl-β-D-ribofuranosyl)indole 1'-deoxy-1'-(5-fluoroindolyl)-β-D-ribofuranose 3-(3-thienyl)-2,5,6-trichloro-1-(2,3-O-isopropylidene-5-O-methoxymethyl-β-D-ribofuranosyl)indole 3-(2-furyl)-2,5,6-trichloro-1-(2,3-O-isopropylidene-5-O-methoxymethyl-β-D-ribofuranosyl)indole 2,5,6-trichloro-3-iodo-1-(β-D-ribofuranosyl)indole β-indolyl-5'-O-(N-salicylsulfamoyl)ribose 3-formyl-2,5,6-trichloro-1-(2,3-O-isopropylidene-β-D-ribofuranosyl)indole 3-formyl-2,5,6-trichloro-1-(2,3-O-isopropylidene-5-O-methoxycarbonyl-β-D-ribofuranosyl)indole 3-cyano-2,5,6-trichloro-1-(2,3-O-isopropylidene-β-D-ribofuranosyl)indole 2,5,6-trichloro-3-propionyl-1-(5-O-acetyl-β-D-ribofuranosyl)indole 3-formyl-2,5,6-trichloro-1-(2,3-O-isopropylidene-5-O-butyryl-β-D-ribofuranosyl)indole 2,5,6-trichloro-3-cyano-1-(β-D-ribofuranosyl)indole 2,5,6-trichloro-3-cyano-1-(5-O-acetyl-β-D-ribofuranosyl)indole