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n-butyl 3,4-dihydro-3-methyl-4-oxoimidazo[5,1-d]-1,2,3,5-tetrazine-8-carboxylate

中文名称
——
中文别名
——
英文名称
n-butyl 3,4-dihydro-3-methyl-4-oxoimidazo[5,1-d]-1,2,3,5-tetrazine-8-carboxylate
英文别名
Butyl 3,4-dihydro-3-methyl-4-oxoimidazo[5,1-d]-1,2,3,5-tetrazine-8-carboxylate;Butyl 3-methyl-4-oxoimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxylate
n-butyl 3,4-dihydro-3-methyl-4-oxoimidazo[5,1-d]-1,2,3,5-tetrazine-8-carboxylate化学式
CAS
——
化学式
C10H13N5O3
mdl
——
分子量
251.245
InChiKey
YTDPVQVGQALUMD-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):
    1.2
  • 重原子数:
    18
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    89.2
  • 氢给体数:
    0
  • 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
    —— 3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carbonyl chloride 113942-58-8 C6H4ClN5O2 213.583
    替莫唑胺 temozolomide 85622-93-1 C6H6N6O2 194.153

反应信息

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文献信息

  • [EN] TEMOZOLOMIDE ANALOGS AND METHODS OF USE<br/>[FR] ANALOGUES DE TÉMOZOLOMIDE ET PROCÉDÉS D'UTILISATION
    申请人:ST JOHNS CANCER INST
    公开号:WO2022026756A1
    公开(公告)日:2022-02-03
    Disclosed herein are compounds and methods for treating cancer, such as glioblastomas.
    本文揭示了用于治疗癌症(如胶质母细胞瘤)的化合物和方法。
  • 抗Epha3抗体修饰修饰的经鼻入脑的纳米粒子及其用途
    申请人:山东绿叶制药有限公司
    公开号:CN110548016A
    公开(公告)日:2019-12-10
    本发明涉及一种经鼻入脑的纳米粒。具体而言,本发明涉及一种抗Epha3抗体修饰的含有化药的纳米粒,用于治疗胶质瘤和医学成像中的用途。
  • Pharmaceutical Composition Comprising Temozolomide Ester
    申请人:Wang Yongfeng
    公开号:US20080044457A1
    公开(公告)日:2008-02-21
    The present invention discloses general formula I of Temozolomide-8-carboxylate compounds, the process for preparation, pharmaceutical compositions comprising the compounds and the use of the compounds and pharmaceutical compositions for the manufacture of an antitumor medicament. The said pharmaceutical composition comprises one or more general formula I Temozolomide-8-carboxylate compounds as active ingredient, together with conventional pharmaceutical carriers. The composition also comprises one or more pharmaceutically acceptable acidic material, optionally second or tertiary alcohol or ester or ether derivatives thereof. The said pharmaceutical composition can be made into various common formulations, particularly oral formulations as well as topically transdermal patches. The present invention also discloses the application of the compounds and the compositions to treat tumor.
    本发明公开了特莫唑酰胺-8-羧酸酯化合物的通用式I,其制备过程,包含该化合物的制药组合物以及用于制造抗肿瘤药物的化合物和制药组合物的用途。所述制药组合物包括一种或多种通用式I特莫唑酰胺-8-羧酸酯化合物作为活性成分,以及常规的制药载体。该组合物还包括一种或多种药学上可接受的酸性物质,可选的第二或第三醇或酯或醚衍生物。该制药组合物可以制成各种常见的配方,特别是口服制剂以及局部透皮贴片。本发明还公开了该化合物和组合物用于治疗肿瘤的应用。
  • PHARMACEUTICAL COMPOSITION COMPRISING TEMOZOLOMIDE ESTER
    申请人:Tianjin Tasly Group Co., Ltd.
    公开号:EP1798234B1
    公开(公告)日:2012-06-13
  • US7579336B2
    申请人:——
    公开号:US7579336B2
    公开(公告)日:2009-08-25
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同类化合物

米托唑胺 氰基替莫唑胺 替莫唑胺 N-[4-(2-氟苯甲酰)-1,3-二甲基-1H-吡唑-5-基]-N-甲基苯酰胺 3-(2H3)甲基-4-氧代-3,4-二氢咪唑并[5,1-d][1,2,3,5]四嗪-8-甲酰胺 3-(2-氯乙基)-N-甲基-4-氧代-3,4-二氢咪唑并[5,1-d][1,2,3,5]四嗪-8-甲酰胺 3-(2-氯乙基)-N,N-二甲基-4-氧代-3,4-二氢咪唑并[5,1-d][1,2,3,5]四嗪-8-甲酰胺 3-(2-氯乙基)-4-氧代-3H-咪唑并(5,1-d)-1,2,3,5-四嗪-8-羧酸 3,4-二氢-3-甲基-4-氧代咪唑并[5,1-D]-1,2,3,5-四嗪-8-甲酰胺酸 3-cyclohexyl-8-(pyrrolidinocarbonyl)imidazo[5,1-d][1,2,3,5]tetrazin-4(3H)-one 3-cyclohexyl-8-(piperidinocarbonyl)imidazo[5,1-d][1,2,3,5]tetrazin-4(3H)-one 3-cyclohexyl-4-oxoimidazo[5,1-d][1,2,3,5]tetrazin-8-N-methylcarboxamide ethyl 3-cyclohexyl-4-oxoimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxylate 3-cyclohexyl-8-(morpholinocarbonyl)imidazo[5,1-d][1,2,3,5]tetrazin-4(3H)-one S-n-butyl 3,4-dihydro-3-methyl-4-oxoimidazo[5,1-d]-1,2,3,5-tetrazine-8-carbothioate 3-(3,5-dimethyl-1H-pyrazol-1-yl)-6-(isopropylthio)-7-phenylimidazo[1,2-b][1,2,4,5]tetrazine 8-(morpholinocarbonyl)-3-(p-tolyl)imidazo[5,1-d][1,2,3,5]tetrazin-4(3H)-one 4-oxo-3-(p-tolyl)imidazo[5,1-d][1,2,3,5]tetrazin-8-N-methylcarboxamide ethyl 4-oxo-3-(p-tolyl)imidazo[5,1-d][1,2,3,5]tetrazine-8-carboxylate 8-(piperidinocarbonyl)-3-(p-tolyl)imidazo[5,1-d][1,2,3,5]tetrazin-4(3H)-one 3,8-dimethylimidazo[5,1-d][1,2,3,5]tetrazin-4(3H)-one 8-acetyl-3-methylimidazo[5,1-d][1,2,3,5]tetrazin-4(3H)-one 3-(4-methylimidazol-1-yl)imidazo[1,2-b][1,2,4,5]tetrazin 3-methyl-4-oxo-N-(sulfamoyloxy)-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide 3-methyl-4-oxo-N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide N,N,3-trimethyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide methyl 3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carbimidothioate hydroiodide N,3-dimethyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide n-octyl 3,4-dihydro-3-methyl-4-oxoimidazo[5,1-d]-1,2,3,5-tetrazine-8-carboxylate 3-[2-(2-{2-[2-(dimethylamino)ethylcarbamoyl]-1-methylimidazol-4-ylcarbamoyl}-1-methylimidazol-4-ylcarbamoyl)-1-methylimidazol-4-yl]-3,4-dihydro-3-methyl-4-oxoimdazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide 3-(5-{5-[2-(dimethylamino)ethylcarbamoyl]-1-methyl-pyrrol-3-ylcarbamoyl}-1-methylpyrrol-3-yl)-3,4-dihydro-3-methyl-4-oxoimdazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide hexyl 3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxylate n-butyl 3,4-dihydro-3-methyl-4-oxoimidazo[5,1-d]-1,2,3,5-tetrazine-8-carboxylate 3-(2-{2-[2-(dimethylamino)ethylcarbamoyl]-1-methylimidazol-4-ylcarbamoyl}-1-methylimidazol-4-yl)-3,4-dihydro-3-methyl-4-oxoimdazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide 3-{2-[2-(dimethylamino)ethylcarbamoyl]-1-methylimidazol-4-yl}-3,4-dihydro-3-methyl-4-oxoimdazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide 8-carbamoyl-3-(2-trimethylsilylethoxy)methylimidazo<5,1-d>-1,2,3,5-tetrazin-4(3H)-one nor-temozolomide ethyl 3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxylate 8-carbamoyl-3-trimethylsilylmethylimidazo<5,1-d>-1,2,3,5-tetrazin-4(3H)-one Temozolomide hydrochloride methyl 3,4-dihydro-3-methyl-4-oxoimidazo[5,1-d]-1,2,3,5-tetrazine-8-carboxylate [3-N-11C,13C-methyl]temozolomide [4-11C-carbonyl]temozolomide [3-N-11C-methyl]temozolomide N-(2,2-dimethoxyethyl)-3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboximidamide hydroiodide 3-(p-chlorophenyl)-8-(piperidinocarbonyl)imidazo[5,1-d][1,2,3,5]tetrazin-4(3H)-one 8-(morpholinocarbonyl)-3-phenylimidazo[5,1-d][1,2,3,5]tetrazin-4(3H)-one 3-(3,5-dimethyl-1H-pyrazol-1-yl)-6-(propylthio)imidazo[1,2-b][1,2,4,5]tetrazine Imidazo[5,1-d][1,2,3,5]tetrazine 3-(2-(N-(4-fluorophenyl)-N-methylamino)ethyl)-4-oxo-3H,4H-imidazo[1,5-d][1,2,3,5]tetrazine-8-carboxamide