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2-amino-9-pentofuranosyl-7,9-dihydro-1H-purine-6,8-dione | 3868-31-3

中文名称
——
中文别名
——
英文名称
2-amino-9-pentofuranosyl-7,9-dihydro-1H-purine-6,8-dione
英文别名
2-amino-9-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,7-dihydropurine-6,8-dione
2-amino-9-pentofuranosyl-7,9-dihydro-1H-purine-6,8-dione化学式
CAS
3868-31-3
化学式
C10H13N5O6
mdl
——
分子量
299.24
InChiKey
FPGSEBKFEJEOSA-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

物化性质

  • 熔点:
    232-235°C
  • 密度:
    2.43±0.1 g/cm3(Predicted)
  • 溶解度:
    DMSO(轻微溶解)、甲醇(轻微溶解、加热、超声处理) 水(轻微溶解、加热、超声处理)
  • 稳定性/保质期:

    遵照规定使用和储存,则不会分解。

计算性质

  • 辛醇/水分配系数(LogP):
    -3.6
  • 重原子数:
    21
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    170
  • 氢给体数:
    6
  • 氢受体数:
    6

安全信息

  • 储存条件:
    存放在阴凉干燥处即可。

SDS

SDS:47efcda23fd5842643aa9c7744e4ef03
查看

制备方法与用途

生物活性 8-Hydroxyguanosine 是氧化应激的系统标记,也可用作氢氧自由基对 RNA 损伤的标记。

靶点

Human 内源性代谢物

注:这里的表格信息被简化为文本描述。

文献信息

  • [EN] IMMUNOMODULATORY CONJUGATES<br/>[FR] CONJUGUÉS IMMUNOMODULATEURS
    申请人:ASCEND BIOPHARMACEUTICALS PTY LTD
    公开号:WO2013067597A1
    公开(公告)日:2013-05-16
    The present invention provides an immunomodulatory compound comprising a carbohydrate polymer comprising mannose, wherein the carbohydrate polymer is conjugated to at least one immune modulator. The present invention also provides for the use of this compound in immunomodulatory compositions for vaccination and gene therapy methods, together with processes for its preparation.
    本发明提供了一种免疫调节化合物,包括一种含有甘露糖碳水化合物聚合物,其中该碳水化合物聚合物与至少一种免疫调节剂结合。本发明还提供了将该化合物用于免疫调节组合物、疫苗和基因治疗方法的用途,以及其制备方法。
  • Composition, synthesis and therapeutic applications of polyamines
    申请人:Murphy A Michael
    公开号:US20050085555A1
    公开(公告)日:2005-04-21
    This invention relates to a process of synthesis and composition of open chain (ring), closed ring, linear branched and or substituted polyamines, polyamine derived tyrosine phosphatase inhibitors and PPAR partial agonists/partial antagonists via a series of substitution reactions and optimizing the bioavailability and biological activities of the compounds. Polyamines prevent the toxicty of neutoxins and diabetogenic toxins including paraquat, methyphenyl pyridine radical, rotenone, diazoxide, streptozotocin and alloxan. These polyamines can be to treat neurological, cardiovascular, endocrine acquired and inherited mitochondrial DNA damage diseases and other disorders in mammalian subjects, and more specifically to the therapy of Parkinson's disease, Alzheimer's disease, Lou Gehrig's disease, Binswanger's disease, Olivopontine Cerebellar Degeneration, Lewy Body disease, Diabetes, Stroke, Atherosclerosis, Myocardial Ischemia, Cardiomyopathy, Nephropathy, Ischemia, Glaucoma, Presbycussis, Cancer, Osteoporosis, Rheumatoid Arthritis, Inflammatory Bowel Disease, Multiple Sclerosis and as Antidotes to Toxin Exposure.
    这项发明涉及一种合成和构成开链(环)、闭环、线性分支和/或取代聚胺、聚胺衍生的酪氨酸磷酸抑制剂PPAR部分激动剂/部分拮抗剂的过程,通过一系列的取代反应来优化化合物的生物利用度和生物活性。聚胺可以预防神经毒素和导致糖尿病的毒素的毒性,包括百草枯、甲基苯基吡啶自由基、洛特侬、重组蛋白酶和阿洛克瑞。这些聚胺可以用于治疗哺乳动物主体中的神经系统、心血管系统、内分泌系统获得性和遗传性线粒体DNA损伤疾病以及其他疾病,更具体地用于治疗帕森病、阿尔茨海默病、路易氏氏病、宾斯旺格氏病、橄榄桥小脑变性、Lewy小体病、糖尿病、中风、动脉粥样硬化、心肌缺血、心肌病、肾病、缺血、青光眼、老年性耳聋、癌症、骨质疏松症、类风湿性关节炎、炎症性肠病、多发性硬化症以及作为毒素暴露的解毒剂。
  • Compositions and Methods for the Inhibition of Methyltransferases
    申请人:Northeastern University
    公开号:US20150057243A1
    公开(公告)日:2015-02-26
    Methods and compositions disclosed herein relate to detecting, analyzing, isolating and inhibiting methyltransferases, methyltransferase substrates, S-adenosyl-methionine-binding proteins and RNA, including for the treatment of disease.
    本文披露的方法和组合与检测、分析、分离和抑制甲基转移酶、甲基转移酶底物、S-腺苷酸结合蛋白和RNA有关,包括用于治疗疾病。
  • [EN] HYBRID COMPOUNDS OF CURCUMIN AND MELATONIN AS NEUROPROTECTANTS FOR NEURODEGENERATIVE DISORDERS<br/>[FR] COMPOSÉS HYBRIDES DE CURCUMINE ET DE MÉLATONINE UTILES EN TANT QUE NEUROPROTECTEURS DANS LES TROUBLES NEURODÉGÉNÉRATIFS
    申请人:UNIV VIRGINIA COMMONWEALTH
    公开号:WO2015069970A1
    公开(公告)日:2015-05-14
    Hybrid compounds of curcumin and melatonin as neuroprotectants are provided. The hybrid compounds are useful for the treatment and/or prevention of Alzheimer's disease (AD), as well as other neurodegenerative diseases. The hybrid compounds exhibited superior and potent neuroprotection in an AD model.
    提供了以姜黄素褪黑素为基础的混合化合物作为神经保护剂。这些混合化合物对治疗和/或预防阿尔茨海默病(AD)以及其他神经退行性疾病具有用处。在AD模型中,这些混合化合物表现出卓越且有效的神经保护作用。
  • Dithiolthione compounds for the treatment of neurological disorders and for memory enhancement
    申请人:Patrick Prendergast
    公开号:US20040053989A1
    公开(公告)日:2004-03-18
    The invention provides methods to treat neurological disorders such as Alzheimer's disease, or to slow the progression of such diseases, or to treat and/or prevent other disorders as disclosed in the specification, by administering to patients, or delivering to the tissues of such patients, oltipraz or related compounds as disclosed in the specification.
    该发明提供了治疗神经系统疾病,如阿尔茨海默病的方法,或减缓这些疾病的进展,或治疗和/或预防其他疾病的方法,通过向患者或向这些患者的组织输送在规范中披露的oltipraz或相关化合物。
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