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2-(sec-butyldisulfanyl)benzo[d]thiazole | 514207-45-5

中文名称
——
中文别名
——
英文名称
2-(sec-butyldisulfanyl)benzo[d]thiazole
英文别名
2-(butan-2-yldisulfanyl)-1,3-benzothiazole
2-(sec-butyldisulfanyl)benzo[d]thiazole化学式
CAS
514207-45-5
化学式
C11H13NS3
mdl
——
分子量
255.429
InChiKey
SEBPGRSSPNLOGD-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):
    4.6
  • 重原子数:
    15
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    91.7
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    1-methyl-1-propanethioisothiourea hydrochloride2-巯基苯并噻唑碳酸氢钠 作用下, 以 甲醇 为溶剂, 以88%的产率得到2-(sec-butyldisulfanyl)benzo[d]thiazole
    参考文献:
    名称:
    Selective Inhibition of Extracellular Thioredoxin by Asymmetric Disulfides
    摘要:
    Whereas the role of mammalian thioredoxin (Trx) as an intracellular protein cofactor is widely appreciated, its function in the extracellular environment is not well-understood. Only few extracellular targets of Trx-mediated thiol disulfide exchange are known. For example, Trx activates extracellular transglutaminase 2 (TG2) via reduction of an intramolecular disulfide bond. Because hyperactive TG2 is thought to play a role in various diseases, understanding the biological role of utracellular Trx may provide critical insight into the pathogenesis of these disorders. Starting from a clinical-stage asymmetric disulfide lead, we have identified analogs with >100-fold specificity for Trx. Structure-activity relationship and computational docking model analyses have provided insights into the features important for enhancing potency and specificity. The most active compound identified had an IC50 below 0.1 mu M in cell culture and may be appropriate for in vivo use to interrogate the role of extracellular Trx in health and disease.
    DOI:
    10.1021/jm301775s
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文献信息

  • Methods and compositions to prevent or treat bacterial infections
    申请人:Ketter Patrick
    公开号:US10398682B2
    公开(公告)日:2019-09-03
    Certain embodiments are directed to methods and compositions for preventing or treating bacterial infections. In certain embodiments the compositions comprise thioredoxin inhibitors, and/or thioredoxin-like inhibitors.
    某些实施方案涉及预防或治疗细菌感染的方法和组合物。在某些实施方案中,组合物包括硫氧还蛋白抑制剂和/或硫氧还蛋白样抑制剂。
  • MODULATION OF TISSUE TRANSGLUTAMINASE ACTIVATION IN DISEASE
    申请人:The Board of Trustees of the Leland Stanford Junior University
    公开号:EP2721169A2
    公开(公告)日:2014-04-23
  • BIOACTIVE SUBSTANCE-BLOOD PROTEIN CONJUGATE AND STABILIZATION OF A BIOACTIVE SUBSTANCE USING THE SAME
    申请人:Park Jong-Il
    公开号:US20100021480A1
    公开(公告)日:2010-01-28
    This invention relates to a technology of modifying low-molecular-weight bioactive substances with short in vivo half-life and low stability in order to achieve a stable and efficient in vivo delivery thereof. More specifically, the present invention relates to a stable bioactive substance-blood protein conjugate, wherein a low-molecular-weight bioactive substance is ex vivo conjugated with a specific functional group on a blood protein through a reactive group, the low-molecular-weight bioactive substance is available as a drug for treatment and prevention in mammals including human and selected from the group consisting of a natural substance; and a method of a stable and efficient in vivo delivery of the low-molecular-weight bioactive substance based on the use of the bioactive substance-blood protein conjugate.
  • Modulation of Tissue Transglutaminase Activation in Disease
    申请人:DiRaimondo Thomas
    公开号:US20140322278A1
    公开(公告)日:2014-10-30
    Compositions and methods are provided for modulating the physiological activation of tissue transglutaminase (TG2); which methods can include inhibiting the activation of TG2 associated with enteric inflammatory disorders, which disorders may include celiac disease, irritable bowel syndrome, Crohn's Disease, dermatitis herpetiformis, and the like. In other embodiments of the invention, methods are provided for reducing undesirable paracellular transport in enteric tissues, in particular the paracellular transport of molecules greater than about 500 mw, e.g. peptides, including without limitation immunogenic gluten peptides.
  • METHODS AND COMPOSITIONS TO PREVENT OR TREAT BACTERIAL INFECTIONS
    申请人:KETTER Patrick
    公开号:US20160151333A1
    公开(公告)日:2016-06-02
    Certain embodiments are directed to methods and compositions for preventing or treating bacterial infections. In certain embodiments the compositions comprise thioredoxin inhibitors, and/or thioredoxin-like inhibitors.
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同类化合物

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