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(R)-1-(5-acetoxyhexyl)-7-benzyl-3-methylxanthine | 301329-56-6

中文名称
——
中文别名
——
英文名称
(R)-1-(5-acetoxyhexyl)-7-benzyl-3-methylxanthine
英文别名
[(2R)-6-(7-benzyl-3-methyl-2,6-dioxopurin-1-yl)hexan-2-yl] acetate
(R)-1-(5-acetoxyhexyl)-7-benzyl-3-methylxanthine化学式
CAS
301329-56-6
化学式
C21H26N4O4
mdl
——
分子量
398.462
InChiKey
BUCWRUDZXPWBKZ-OAHLLOKOSA-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):
    2.5
  • 重原子数:
    29
  • 可旋转键数:
    9
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    84.7
  • 氢给体数:
    0
  • 氢受体数:
    5

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
  • 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:
    参考文献:
    名称:
    Therapeutic compounds for inhibiting interleukin-12 signals and method for using same
    摘要:
    发现将六元环结构融合到五元环结构的新型杂环化合物对治疗和预防与受白细胞介素-12(“IL-12”)胞内信号传导受影响的疾病相关的症状或表现是有用的,例如Th1细胞介导的疾病。这些治疗化合物、药学上可接受的衍生物(例如,其解旋异构体、二对映异构体、互变异构体、盐和溶剂)或其前药具有以下一般公式:每个X、Y和Z独立地选择自C(R3)、N、N(R3)和S的群体之一。每个R1、R2和R3被取代或未取代,并且独立地选择自氢、卤、氧、C(1-20)烷基、C(1-20)羟基烷基、C(1-20)硫烷基、C(1-20)烷基胺、C(1-20)烷基胺烷基、C(1-20)胺基烷基、C(1-20)胺基甲氧基烯基、C(1-20)胺基甲氧基炔基、C(1-20)二胺基烷基、C(1-20)三胺基烷基、C(1-20)四胺基烷基、C(5-15)氨基三烷氧基氨基、C(1-20)烷基酰胺、C(1-20)烷基酰胺烷基、C(1-20)酰胺基烷基、C(1-20)乙酰胺基烷基、C(1-20)烯基、C(1-20)炔基、C(3-8)烷氧基、C(1-11)烷氧基烷基和C(1-20)二烷氧基烷基。
    公开号:
    US06878715B1
  • 作为产物:
    描述:
    (R)-5-acetoxy-1-bromohexane 、 7-苄基-3-甲基黄嘌呤二甲基亚砜 为溶剂, 以76%的产率得到(R)-1-(5-acetoxyhexyl)-7-benzyl-3-methylxanthine
    参考文献:
    名称:
    TRICYCLIC FUSED XANTHINE COMPOUNDS AND THEIR USES
    摘要:
    发现新型三环化合物对于治疗或预防受细胞因子内部信号传导影响的疾病或疾病相关症状或表现具有益处。
    公开号:
    US20020103211A1
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文献信息

  • Therapeutic compounds for inhibiting interleukin-12 signaling and methods for using same
    申请人:Klein Peter J.
    公开号:US20050049262A1
    公开(公告)日:2005-03-03
    Novel heterocyclic compounds having a six membered ring structure fused to a five membered ring structure are found to be useful for the treatment and prevention of symptoms or manifestations associated with disorders affected by lnterleukin-12 (“IL-12”) intracellular signaling, such as, for example, Th1 cell-mediated disorders. The therapeutic compounds, pharmaceutically acceptable derivatives (e.g., resolved enantiomers, diastereomers, tautomers, salts and solvates thereof) or prodrugs thereof, have the following general formula: Each X, Y and Z are independently selected from a member of the group consisting of C(R 3 ), N, N(R 3 ) and S. Each R 1 , R 2 and R 3 is substituted or unsubstituted and is independently selected from a member of the group consisting of hydrogen, halo, oxo, C (1-20) alkyl, C (1-20) hydroxyalkyl, C (1-20) thioalkyl, C (1-20) alkylamino, C (1-20) alkylaminoalkyl, C (1-20) aminoalkyl, C (1-20) aminoalkoxyalkenyl, C (1-20) aminoalkoxyalkynyl, C (1-20) diaminoalkyl, C (1-20) triaminoalkyl, C (1-20) tetraaminoalkyl, C (5-15) aminotrialkoxyamino, C (1-20) alkylamido, C (1-20) alkylamidoalkyl, C (1-20) amidoalkyl, C (1-20) acetamidoalkyl, C (1-20) alkenyl, C (1-20) alkynyl, C (3-8) alkoxyl, C (1-11) alkoxyalkyl, and C (1-20) dialkoxyalkyl.
    具有六元环结构融合到五元环结构的新型杂环化合物被发现可用于治疗和预防与受白细胞介素-12(“IL-12”)细胞内信号传导影响的疾病症状或表现,例如Th1细胞介导的疾病。治疗化合物,药学上可接受的衍生物(例如,解析对映体,非对映体,互变异构体,其盐和溶剂化物)或其前药,具有以下通用公式: 每个X,Y和Z独立地从C(R3),N,N(R3)和S组成的组中选择。每个R1,R2和R3被取代或未取代,并且独立地从氢,卤素,氧代,C(1-20)烷基,C(1-20)羟基烷基,C(1-20)代烷基,C(1-20)烷基基,C(1-20)烷基基烷基,C(1-20)基烷基,C(1-20)基烷氧基烯基,C(1-20)基烷氧基炔基,C(1-20)二基烷基,C(1-20)三基烷基,C(1-20)四基烷基,C(5-15)基三烷氧基基,C(1-20)烷基酰胺基,C(1-20)烷基酰胺基烷基,C(1-20)酰胺基烷基,C(1-20)乙酰胺基烷基,C(1-20)烯基,C(1-20)炔基,C(3-8)烷氧基,C(1-11)烷氧基烷基和C(1-20)二烷氧基烷基中独立选择。
  • Tricyclic compounds and their uses
    申请人:——
    公开号:US20030162801A1
    公开(公告)日:2003-08-28
    Novel tricyclic compounds are found to be useful for the treatment or prevention of symptoms or manifestations associated with diseases or disorders affected by cytokine intracellular signaling.
    新型三环化合物被发现对治疗或预防受细胞因子内部信号传导影响的疾病或疾病症状或表现有用。
  • Tricyclic fused xanthine compounds and their uses
    申请人:Cell Therapeutics, Inc.
    公开号:US06586429B2
    公开(公告)日:2003-07-01
    Novel tricyclic compounds are found to be useful for the treatment or prevention of symptoms or manifestations associated with diseases or disorders affected by cytokine intracellular signaling. The compounds have the following formulas where R1, R2 and R3 are defined in the written description of the invention.
    新型三环化合物被发现对于治疗或预防受细胞因子内部信号传递影响的疾病或障碍相关的症状或表现非常有用。这些化合物具有以下公式,其中R1,R2和R3在发明的书面描述中有定义。
  • Uses of tricyclic compounds
    申请人:Cell Therapeutics, Inc.
    公开号:US07247630B2
    公开(公告)日:2007-07-24
    Novel tricyclic compounds are disclosed having the general structure of Formulas I or II: were R1, R2 and R3 are defined in the written description of the invention. The compounds are useful for the treatment or prevention of symptoms or manifestations associated with diseases or disorders affected by intracellular cytokine signaling.
    本发明揭示了具有I或II式一般结构的新型三环化合物:其中R1、R2和R3在发明的书面描述中有定义。该化合物可用于治疗或预防由细胞内细胞因子信号传导影响的疾病或疾病表现的症状或表现。
  • Tricyclic purine compounds and their analogs as inhibitors of cytokine signalling
    申请人:CELL THERAPEUTICS, INC.
    公开号:EP1690864A2
    公开(公告)日:2006-08-16
    Novel tricyclic compounds are found to be useful for the treatment or prevention of symptoms or manifestations associated with diseases or disorders affected by cytokine intracellular signaling.
    新型三环化合物可用于治疗或预防与受细胞因子细胞内信号传导影响的疾病或紊乱有关的症状或表现。
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