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2-(oxalylamino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylic acid

中文名称
——
中文别名
——
英文名称
2-(oxalylamino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylic acid
英文别名
1C88;2-(Oxalyl-amino)-4,5,6,7-tetrahydro-thieno[2,3-C]pyridine-3-carboxylic acid;2-(oxaloamino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylic acid
2-(oxalylamino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylic acid化学式
CAS
——
化学式
C10H10N2O5S
mdl
——
分子量
270.266
InChiKey
ZIBMATWHOAGNTR-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):
    -1.7
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    144
  • 氢给体数:
    4
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    2-(tert-butoxyoxalylamino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3,6-dicarboxylic acid di-tert-butyl ester 在 三氟乙酸 作用下, 以 二氯甲烷 为溶剂, 反应 16.0h, 以88%的产率得到2-(oxalylamino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylic acid
    参考文献:
    名称:
    Discovery and SAR of a Novel Selective and Orally Bioavailable Nonpeptide Classical Competitive Inhibitor Class of Protein-Tyrosine Phosphatase 1B
    摘要:
    Reversible phosphorylation and dephosphorylation of key proteins on tyrosine residues are important parts of intracellular signaling triggered by hormones and other agents. Recent knock-out studies in mice have identified PTP1B as a potential target for the treatment of diabetes and obesity. As a consequence, a number of academic and industrial groups are aggressively pursuing the development of selective PTP1B inhibitors. In addition, other protein-tyrosine phosphatases (PTPs) appear to be critically involved in major diseases such as cancer and autoimmunity. Given the diversity of PTPs and their potential as drug targets in different diseases, we have taken a broad approach to develop active site-directed selective inhibitors of specific members of this family of enzymes. Using a high throughput screening, we have previously identified 2-(oxalylamino)benzoic acid 3a as a relatively weak but classical competitive inhibitor of several PTPs.(4) On the basis of our early studies, indicating that 3a might be used as a starting point for the synthesis of selective PTP inhibitors, we now present our efforts in expansion of this concept and provide here a number of new chemical scaffolds for the development of inhibitors of different members of the PTP family. Although the core structure of these inhibitors is charged, good oral bioavailability has been observed in rat for some compounds. Furthermore, we have observed enhancement of 2-deoxy-glucose accumulation in C2C12 cells with prodrug analogues.
    DOI:
    10.1021/jm0209026
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文献信息

  • Rhodanine Derivatives, a Process for the Preparation Thereof and Pharmaceutical Composition Containing the Same
    申请人:Ryu Seong Eon
    公开号:US20090042872A1
    公开(公告)日:2009-02-12
    Disclosed herein are rhodanine derivatives, a method for the preparation thereof, and a pharmaceutical composition containing the same. The rhodanine derivatives have inhibitory activity against protein phosphatases (PPase) such as PTP1B, Prl-3, LAR, CD45, Cdc25A, Cdc25B, Cdc25C, Yop, PP1 and VHR, and can be applied for the prevention and treatment of PPase-caused diseases, including autoimmune diseases, diabetes, impaired glucose intolerance, insulin resistance, obesity, cancers, etc. when the inhibitory activity thereof is modulated.
    本文披露了罗丹宁生物、其制备方法以及含有相同物质的药物组合物。这些罗丹宁生物具有对蛋白磷酸酶(PPase)如PTP1B、Prl-3、LAR、CD45、Cdc25A、Cdc25B、Cdc25C、Yop、PP1和VHR的抑制活性,并可用于预防和治疗PPase引起的疾病,包括自身免疫疾病、糖尿病、糖耐量受损、胰岛素抵抗、肥胖、癌症等,当其抑制活性被调节时。
  • Synthesis of tetrasubstituted thiophenes on solid-support using the Gewald reaction
    作者:Georgette M Castanedo、Daniel P Sutherlin
    DOI:10.1016/s0040-4039(01)01470-8
    日期:2001.10
    The Gewald reaction was performed on solid support. This reaction combines a ketone or aldehyde, an activated nitrile, and sulfur in the presence of a suitable amine base to make tri- and tetrasubstituted thiophenes. After optimizing conditions for maximum yield and purity, the scope of the reaction was investigated. Finally, this method is highlighted in the synthesis of two biologically relevant
    Gewald反应在固体载体上进行。该反应在合适的胺碱的存在下将酮或醛,活化的腈和结合以制备三和四取代的噻吩。优化了最大产率和纯度的条件后,研究了反应范围。最后,在两种生物学上相关的化合物的合成中突出了该方法。
  • Modulators of protein tyrosine phosphatases (PTPases)
    申请人:——
    公开号:US20030069267A1
    公开(公告)日:2003-04-10
    The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTP&agr;, LAR and HePTP or the like. The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.
    本发明提供了新型化合物、新型组合物、它们的使用方法和制造方法,其中这些化合物是药理学上有用的蛋白酪氨酸磷酸酶(PTPase's)抑制剂,如PTP1B、CD45、SHP-1、SHP-2、PTP&agr;、LAR和HePTP等。这些化合物可用于治疗I型糖尿病、II型糖尿病、糖耐量受损、胰岛素抵抗、肥胖症、免疫功能障碍,包括凝血系统功能障碍的自身免疫性疾病、包括哮喘在内的过敏性疾病、骨质疏松症、增生性疾病,包括癌症和屑病、合成减少或增加或对生长激素释放或响应调节的激素或细胞因子的疾病,包括阿尔茨海默病和精神分裂症的脑部疾病以及传染病。
  • Advanced drug development and manufacturing
    申请人:Los Alamos National Security, LLC
    公开号:EP2511844A2
    公开(公告)日:2012-10-17
    There is described an apparatus for measuring protein characteristics comprising an X-ray fluorescence (XRF) spectrometer comprising a source of polychromatic X-rays, an X-ray detector, a protein, a molecule that has been exposed to and at least weakly binds to the protein, a plurality of X-ray fluorescence signal data obtained by irradiating chemical elements in the protein and molecule with the polychromatic X-rays and a security system for maintaining records for the data from the plurality of X-ray fluorescence signal measurements. There is also described an x-ray microscope for measuring a sample.
    描述了一种测量蛋白质特性的仪器,该仪器包括一个 X 射线荧光 (XRF) 光谱仪,其中包括一个多色 X 射线源、一个 X 射线探测器、一个蛋白质、一个已暴露于该蛋白质并至少与该蛋白质弱结合的分子、通过用多色 X 射线照射蛋白质和分子中的化学元素而获得的多个 X 射线荧光信号数据,以及一个用于维护多个 X 射线荧光信号测量数据记录的安全系统。此外,还介绍了一种用于测量样品的 X 射线显微镜。
  • MODULATORS OF PROTEIN TYROSINE PHOSPHATASES (PTPASES)
    申请人:NOVO NORDISK A/S
    公开号:EP1080095B1
    公开(公告)日:2005-11-02
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