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(8-(2-chlorophenyl)-2-methyl-6-(4-methylpiperazin-1-yl)-9-(tetrahydro-2H-pyran-4-yl)-9H-purine) | 1231220-79-3

中文名称
——
中文别名
——
英文名称
(8-(2-chlorophenyl)-2-methyl-6-(4-methylpiperazin-1-yl)-9-(tetrahydro-2H-pyran-4-yl)-9H-purine)
英文别名
LY2828360;8-(2-Chlorophenyl)-2-methyl-6-(4-methylpiperazin-1-yl)-9-(tetrahydro-2H-pyran-4-yl)-9H-purine;8-(2-chlorophenyl)-2-methyl-6-(4-methylpiperazin-1-yl)-9-(oxan-4-yl)purine
(8-(2-chlorophenyl)-2-methyl-6-(4-methylpiperazin-1-yl)-9-(tetrahydro-2H-pyran-4-yl)-9H-purine)化学式
CAS
1231220-79-3
化学式
C22H27ClN6O
mdl
——
分子量
426.949
InChiKey
UCMNDPDJRSEZPL-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):
    3.3
  • 重原子数:
    30
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    59.3
  • 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

反应信息

  • 作为反应物:
    描述:
    (8-(2-chlorophenyl)-2-methyl-6-(4-methylpiperazin-1-yl)-9-(tetrahydro-2H-pyran-4-yl)-9H-purine)磷酸 作用下, 以 乙醇 为溶剂, 生成 8-(2-chlorophenyl)-2-methyl-6-(4-methylpiperazin-1-yl)-9-(tetrahydropyran-4-yl)-9H-purine phosphate
    参考文献:
    名称:
    Purine Compounds
    摘要:
    该化合物的分子式为,并且用于治疗疼痛的药物组合。
    公开号:
    US20100160288A1
  • 作为产物:
    参考文献:
    名称:
    The Development of Practical Synthetic Routes to a CB2 Agonist: Efficient Construction of a Densely Substituted Purine Core
    摘要:
    An efficient and scalable process for the preparation of a purine-based CB2 agonist was developed. The production route to the requisite purine core relies on N-acylation and sequential substitution of a 5-amino-4,6-dichloropyrimidine with two amine building blocks followed by a cyclocondensation reaction. The chemistry was successfully employed to rapidly prepare over S kg of the active pharmaceutical ingredient. To further improve efficiencies, postproduction development resulted in a rearranged synthesis which reduced the need for pressure reactors and introduced the most costly reagent in the final step.
    DOI:
    10.1021/op300278c
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文献信息

  • Purine compounds
    申请人:Eli Lilly and Company
    公开号:US08252798B2
    公开(公告)日:2012-08-28
    A compound of the formula: and pharmaceutical compositions for the treatment of pain.
    公式为:的化合物以及用于治疗疼痛的药物组合物。
  • Selective Cannabinoid Receptor Type 2 (CB2) Agonists: Optimization of a Series of Purines Leading to the Identification of a Clinical Candidate for the Treatment of Osteoarthritic Pain
    作者:Sean P. Hollinshead、Michael W. Tidwell、John Palmer、Rossella Guidetti、Adam Sanderson、Michael P. Johnson、Mark G. Chambers、Jennifer Oskins、Robert Stratford、Peter C. Astles
    DOI:10.1021/jm400305d
    日期:2013.7.25
    A focused screening strategy identified thienopyrimidine 12 as a cannabinoid receptor type 2 agonist (hCB2) with moderate selectivity over the hCB1 receptor. This initial hit suffered from poor in vitro metabolic stability and high in vivo clearance. Structure-activity relationships describe the optimization and modification to a new more polar series of purine CB2 agonists. Examples from this novel scaffold were found to be highly potent and fully efficacious agonists of the human CB2 receptor with excellent selectivity against CBI, often having no CBI agonist activity at the highest concentration measured (>100 mu M). Compound 26 is a centrally penetrant molecule which possesses good biopharmaceutical properties, is highly water-soluble, and demonstrates robust oral activity in rodent models of joint pain. In addition, the peripherally restricted molecule 22 also demonstrated significant efficacy in the same analgesic model of rodent inflammatory pain.
  • PURINE COMPOUNDS
    申请人:Eli Lilly and Company
    公开号:EP2379555A1
    公开(公告)日:2011-10-26
  • METHODS OF USING CANNABINOID CB2 RECEPTOR AGONIST COMPOSITIONS TO SUPPRESS AND PREVENT OPIOID TOLERANCE AND WITHDRAWAL IN A SUBJECT
    申请人:Indiana University Research and Technology Corporation
    公开号:US20190314379A1
    公开(公告)日:2019-10-17
    The present disclosure relates to methods of using cannabinoid CB 2 receptor agonist compositions to suppress pain (e.g., neuropathic pain), opioid tolerance, and/or opioid-induced physical dependence in a subject.
  • US8252798B2
    申请人:——
    公开号:US8252798B2
    公开(公告)日:2012-08-28
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