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2-phenyl-7(9)H-purin-6-ylamine | 1501-45-7

中文名称
——
中文别名
——
英文名称
2-phenyl-7(9)H-purin-6-ylamine
英文别名
2-Phenyl-7(9)H-purin-6-ylamin;2-phenyl-7H-purin-6-amine
2-phenyl-7(9)<i>H</i>-purin-6-ylamine化学式
CAS
1501-45-7
化学式
C11H9N5
mdl
——
分子量
211.226
InChiKey
YKMJOAVCSAOXOU-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):
    1.4
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    80.5
  • 氢给体数:
    2
  • 氢受体数:
    4

SDS

SDS:33771d70fa34d221f8a32d7df9c7f5cb
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反应信息

  • 作为反应物:
    描述:
    2-phenyl-7(9)H-purin-6-ylamine4-三氟甲基苯基异氰酸酯三乙胺 作用下, 反应 1.0h, 以54.5%的产率得到N6-(4-trifluoromethylphenylcarbamoyl)-2-phenyladenine
    参考文献:
    名称:
    新型 2-苯基腺嘌呤和 2-苯基蝶呤的合成及作为腺苷受体配体的生物学评价
    摘要:
    描述了一系列 2-苯基蝶啶衍生物的合成和生物测定,以将它们对腺苷受体的亲和力与特意制备的相应腺嘌呤和先前描述的 8-氮杂腺嘌呤的亲和力进行比较。这项研究表明,腺嘌呤核的五元环扩大为六元环是一种修饰,不允许分子保持对腺苷受体的高活性;事实上,蝶啶衍生物本身并不是良好的腺苷受体配体。相反,N6-环烷基-或N6-烷基-2-苯基腺嘌呤对A1腺苷受体表现出非常高的亲和力和选择性。我们还证明了 9-苄基取代基对于将 A3 受体的高亲和力赋予具有 2-苯腺嘌呤样核的分子至关重要。
    DOI:
    10.1002/ardp.200600168
  • 作为产物:
    描述:
    5-亚硝基-2-苯基嘧啶-4,6-二胺 在 sodium dithionite 、 乙酸酐 作用下, 生成 2-phenyl-7(9)H-purin-6-ylamine
    参考文献:
    名称:
    Synthesis of 2-Aminonicotinamides by Raney Nickel Cleavage of Pyrazolo[3,4-b]-pyridines1
    摘要:
    DOI:
    10.1021/ja01519a043
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文献信息

  • Aqueous-Phase Suzuki-Miyaura Cross-Coupling Reactions of Free Halopurine Bases
    作者:Michal Hocek、Petr Čapek、Milan Vrábel、Zbyněk Hasník、Radek Pohl
    DOI:10.1055/s-2006-950240
    日期:2006.10
    The Suzuki-Miyaura reaction of 9-unsubstituted 2-, 6-, and 8-halopurine bases with diverse aryl- and alkenylboronic acids in water-acetonitrile mixtures under microwave irradiation was used for the single-step synthesis of arylpurines. In most cases the product crystallized directly from the reaction mixture in high yields and good purity. The scope and limitations of these reactions were studied.
    通过水-乙腈混合物中微波辐照下,9-未取代的2-、6-和8-卤代嘌呤碱与多种芳基和烯基硼酸的Suzuki-Miyaura反应,实现了单步合成芳基嘌呤。在大多数情况下,产物以高产率直接从反应混合物中结晶,纯度良好。研究了这些反应的范围和局限性。
  • Method for treating disease or condition susceptible to amelioration by AMPK activators and compounds of formula which are useful to activate AMP-activated protein kinase (AMPK)
    申请人:CHEN Han-Min
    公开号:US20140303112A1
    公开(公告)日:2014-10-09
    The present invention relates to a method for treating disease or condition susceptible to amelioration by AMPK activators and compounds of formula which are useful to activate AMP-activated protein kinase (AMPK) and the use of the compounds in the prevention or treatment of disease, including pre-diabetes, type 2 diabetes, syndrome X, metabolic syndrome and obesity.
    本发明涉及一种治疗疾病或病情的方法,该疾病或病情容易通过AMPK激活剂和公式化合物得到改善,这些化合物有助于激活AMP激活蛋白激酶(AMPK),并将这些化合物用于预防或治疗疾病,包括糖尿病前期、2型糖尿病、X综合症、代谢综合征和肥胖症。
  • Stem Cell Culture Methods
    申请人:Adams David Roger
    公开号:US20120202287A1
    公开(公告)日:2012-08-09
    The invention provides methods for reversibly inhibiting stem cell differentiation wherein a compound of formula (I) is contacted with a stem cell. The invention further provides a method for preparing a culture medium, a culture medium supplement and a composition comprising a compound of formula (I).
    该发明提供了一种可逆抑制干细胞分化的方法,其中将式(I)的化合物与干细胞接触。该发明还提供了一种制备培养基、培养基添加剂和包含式(I)化合物的组合物的方法。
  • Methods and systems for genetic analysis
    申请人:Personalis, Inc.
    公开号:US10415091B2
    公开(公告)日:2019-09-17
    This disclosure provides systems and methods for sample processing and data analysis. Sample processing may include nucleic acid sample processing and subsequent sequencing. Some or all of a nucleic acid sample may be sequenced to provide sequence information, which may be stored or otherwise maintained in an electronic storage location. The sequence information may be analyzed with the aid of a computer processor, and the analyzed sequence information may be stored in an electronic storage location that may include a pool or collection of sequence information and analyzed sequence information generated from the nucleic acid sample. Methods and systems of the present disclosure can be used, for example, for the analysis of a nucleic acid sample, for producing one or more libraries, and for producing biomedical reports. Methods and systems of the disclosure can aid in the diagnosis, monitoring, treatment, and prevention of one or more diseases and conditions.
    本公开提供了用于样本处理和数据分析的系统和方法。样本处理可包括核酸样本处理和后续测序。可对部分或全部核酸样本进行测序,以提供序列信息,该信息可存储或以其他方式保存在电子存储位置中。序列信息可借助计算机处理器进行分析,分析后的序列信息可存储在电子存储位置中,该电子存储位置可包括序列信息池或序列信息集合,以及由核酸样本生成的分析后序列信息。本公开的方法和系统可用于分析核酸样本、生成一个或多个文库以及生成生物医学报告等。本公开的方法和系统可帮助诊断、监测、治疗和预防一种或多种疾病和病症。
  • Compositions and methods for improving plastid transformation efficiency in higher plants
    申请人:RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY
    公开号:US11208665B2
    公开(公告)日:2021-12-28
    Compositions and methods for improving plastid transformation in difficult to transform plants are disclosed.
    本发明公开了用于改善难以转化植物的质体转化的组合物和方法。
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