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cyclopropavir

中文名称
——
中文别名
——
英文名称
cyclopropavir
英文别名
2-amino-9-{[(1Z)-2,2-bis(hydroxymethyl)cyclopropylidene]methyl}-6,9-dihydro-1H-purin-6-one;2-amino-9-[[2,2-bis(hydroxymethyl)cyclopropylidene]methyl]-1H-purin-6-one
cyclopropavir化学式
CAS
——
化学式
C11H13N5O3
mdl
——
分子量
263.256
InChiKey
KMUNHOKTIVSFRA-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):
    -1.9
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    126
  • 氢给体数:
    4
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    cyclopropavir 在 human herpesvirus 6A U69 protein kinase with glutathione S-transferase 、 potassium chloride 、 5’-三磷酸腺苷 、 magnesium chloride 、 1,4-二巯基-2,3-丁二醇 作用下, 以 aq. buffer 为溶剂, 反应 24.0h, 生成
    参考文献:
    名称:
    Human Herpesvirus 6 U69 Kinase Phosphorylates the Methylenecyclopropane Nucleosides Cyclopropavir, MBX 2168, and MBX 1616 to Their Monophosphates
    摘要:
    摘要 二羟甲基和一羟甲基亚甲基环丙烷核苷是人类疱疹病毒 6(HHV-6)两种变体的有效抑制剂。我们研究了 HHV-6 U69 蛋白激酶参与其作用机制的情况。我们研究了二羟甲基类似物环丙沙韦和含 6-醚基(MBX 2168)或 6-硫醚基(MBX 1616)的单羟甲基核苷与纯化的 U69 的磷酸化作用。这三种化合物都是这种病毒激酶的底物,具有相似的迈克尔-门顿动力学参数。
    DOI:
    10.1128/aac.00978-13
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文献信息

  • 2,2-bis-(hydroxymethyl)cyclopropylidenemethyl-purines and pyrmindines as antiviral agents
    申请人:Zemlicka Jiri
    公开号:US20050113393A1
    公开(公告)日:2005-05-26
    Compounds which are active against viruses have the following formulas: wherein B is a purine or pyrimidine heterocyclic ring or base. In a preferred embodiment, the purine include 6-aminopurine (adenine), 6-hydroxypurine (hypoxanthine), 2-amino-6-hydroxypurine (guanine), 2,6-diamino-purine, 2-amino-6-azidopurine, 2-amino-6-halo substituted purines such as 2-amino-6-chloropurine, 2-amino-6-fluoropurine, 2-amino-6-alkoxypurines such as 2-amino-6-methoxypurine, 2-amino-6-cyclopropylaminopurine, 2-amino-6-alkylamino or 2-amino-6-dialkylamino substituted purines, 2-amino-6-thiopurine, 2-amino-6-alkylthio substituted purines, 3-deazapurines, 7-deazapurines and 8-azapurines. The pyrimidine incorporates cytosine, uracil and thymine, 5-halo substituted cytosines and uracils, 5-alkyl substituted cytosines and uracils including derivatives with a saturated or unsaturated alkyl group and 6-azapyrimidines.
    具有抗病毒活性的化合物具有以下公式:其中B是嘌呤或嘧啶杂环环或碱基。在一个首选实施例中,嘌呤包括6-氨基嘌呤(腺嘌呤)、6-羟基嘌呤(次黄嘌呤)、2-氨基-6-羟基嘌呤(鸟嘌呤)、2,6-二氨基嘌呤,2-氨基-6-叠氮基嘌呤,2-氨基-6-卤代嘌呤,例如2-氨基-6-氯嘌呤,2-氨基-6-氟嘌呤,2-氨基-6-烷氧基嘌呤,例如2-氨基-6-甲氧基嘌呤,2-氨基-6-环丙基氨基嘌呤,2-氨基-6-烷基氨基或2-氨基-6-二烷基氨基嘌呤,2-氨基-6-硫嘌呤,2-氨基-6-烷硫代嘌呤,3-脱氮嘌呤,7-脱氮嘌呤和8-氮嘌呤。嘧啶包括胞嘧啶、尿嘧啶和胸腺嘧啶,5-卤代胞嘧啶和尿嘧啶,5-烷基代胞嘧啶和尿嘧啶,包括具有饱和或不饱和烷基基团的衍生物和6-氮杂嘧啶。
  • 2,2-Bis-(hydroxymethyl)cyclopropylidenemethyl-Purines and -Pyrimidines As Antiviral Agents
    申请人:Zemlicka Jiri
    公开号:US20090118308A1
    公开(公告)日:2009-05-07
    Compounds which are active against viruses have the following formulas: wherein B is a purine or pyrimidine heterocyclic ring or base. In a preferred embodiment, the purine include 6-aminopurine (adenine), 6-hydroxypurine (hypoxanthine), 2-amino-6-hydroxypurine (guanine), 2,6-diamino-purine, 2-amino-6-azidopurine, 2-amino-6-halo substituted purines such as 2-amino-6-chloropurine, 2-amino-6-fluoropurine, 2-amino-6-alkoxypurines such as 2-amino-6-methoxypurine, 2-amino-6-cyclopropylaminopurine, 2-amino-6-alkylamino or 2-amino-6-dialkylamino substituted purines, 2-amino-6-thiopurine, 2-amino-6-alkylthio substituted purines, 3-deazapurines, 7-deazapurines and 8-azapurines. The pyrimidine incorporates cytosine, uracil and thymine, 5-halo substituted cytosines and uracils, 5-alkyl substituted cytosines and uracils including derivatives with a saturated or unsaturated alkyl group and 6-azapyrimidines.
    对病毒具有活性的化合物具有以下公式:其中B是嘌呤或嘧啶杂环环或碱基。在优选实施例中,嘌呤包括6-氨基嘌呤(腺嘌呤),6-羟基嘌呤(次黄嘌呤),2-氨基-6-羟基嘌呤(鸟嘌呤),2,6-二氨基嘌呤,2-氨基-6-叠氮基嘌呤,2-氨基-6-卤代嘌呤,例如2-氨基-6-氯嘌呤,2-氨基-6-氟嘌呤,2-氨基-6-烷氧基嘌呤,例如2-氨基-6-甲氧基嘌呤,2-氨基-6-环丙基氨基嘌呤,2-氨基-6-烷基氨基或2-氨基-6-二烷基氨基取代的嘌呤,2-氨基-6-硫代嘌呤,2-氨基-6-烷基硫代取代嘌呤,3-去氮嘌呤,7-去氮嘌呤和8-氮杂嘧啶。嘧啶包括胞嘧啶,尿嘧啶和胸腺嘧啶,5-卤代胞嘧啶和尿嘧啶,5-烷基取代的胞嘧啶和尿嘧啶,包括具有饱和或不饱和烷基的衍生物和6-氮杂嘧啶。
  • 2,2-BIS-(HYDROXYMETHYL)CYCLOPROPYLIDENEMETHYL-PURINES AND -PYRIMIDINES AS ANTIVIRAL AGENTS
    申请人:Zemlicka Jiri
    公开号:US20110275652A1
    公开(公告)日:2011-11-10
    Compounds which are active against viruses have the following formulas: wherein B is a purine or pyrimidine heterocyclic ring or base. In a preferred embodiment, the purine include 6-aminopurine (adenine), 6-hydroxypurine (hypoxanthine), 2-amino-6-hydroxypurine (guanine), 2,6-diamino-purine, 2-amino-6-azidopurine, 2-amino-6-halo substituted purines such as 2-amino-6-chloropurine, 2-amino-6-fluoropurine, 2-amino-6-alkoxypurines such as 2-amino-6-methoxypurine, 2-amino-6-cyclopropylaminopurine, 2-amino-6-alkylamino or 2-amino-6-dialkylamino substituted purines, 2-amino-6-thiopurine, 2-amino-6-alkylthio substituted purines, 3-deazapurines, 7-deazapurines and 8-azapurines. The pyrimidine incorporates cytosine, uracil and thymine, 5-halo substituted cytosines and uracils, 5-alkyl substituted cytosines and uracils including derivatives with a saturated or unsaturated alkyl group and 6-azapyrimidines.
    具有抗病毒活性的化合物具有以下公式:其中B是一种嘌呤或嘧啶杂环环或碱基。在优选实施例中,嘌呤包括6-氨基嘌呤(腺嘌呤)、6-羟基嘌呤(次黄嘌呤)、2-氨基-6-羟基嘌呤(鸟嘌呤)、2,6-二氨基嘌呤、2-氨基-6-叠氮基嘌呤、2-氨基-6-卤代嘌呤,例如2-氨基-6-氯嘌呤、2-氨基-6-氟嘌呤、2-氨基-6-烷氧基嘌呤,例如2-氨基-6-甲氧基嘌呤、2-氨基-6-环丙胺基嘌呤、2-氨基-6-烷基氨基或2-氨基-6-二烷基氨基取代的嘌呤,2-氨基-6-硫代嘌呤,2-氨基-6-烷基硫代取代的嘌呤,3-脱氮嘌呤,7-脱氮嘌呤和8-氮杂嘧啶。嘧啶包括胞嘧啶、尿嘧啶和胸腺嘧啶,5-卤代胞嘧啶和尿嘧啶,5-烷基取代的胞嘧啶和尿嘧啶,包括具有饱和或不饱和烷基的衍生物和6-氮杂嘧啶。
  • 2,2-BIS(HYDROXYMETHYL)CYCLOPROPYLIDENEMETHYL - PURINES AND -PYRIMIDINES AS ANTIVIRAL AGENTS
    申请人:WAYNE STATE UNIVERSITY
    公开号:EP1490368B1
    公开(公告)日:2011-08-03
  • CANCER TREATMENT WITH (2,2-BISHYDROXYMETHYL) METHYLENECYCLOPROPANE NUCLEOTIDES
    申请人:MEDIVIR AB
    公开号:US20200399295A1
    公开(公告)日:2020-12-24
    The invention provides a compound of formula (I) wherein B is a nucleobase; U is O or S; R x is —OC(═O)R y , —OC(═O)CH(R y )NH 2 , —OCH 2 OC(═O)R y ; R y is optionally substituted alkyl or alkenyl or the side chain of a natural or unnatural amino acid R 1 is H, or optionally substituted phenyl, benzyl, naphthyl, pyridyl or indolyl, or R x and R 1 together define a bond thus forming a cyclic phosphate; R 2 and R 2′ together define the side chain of a natural or unnatural amino acid; R 3 is optionally substituted alkyl, cycloalkyl, phenyl or benzyl; and pharmaceutically acceptable salts and compositions thereof which are useful in the treatment of cancer, especially leukemias.
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