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N-(thiophen-2-ylmethyl)hexanamide

中文名称
——
中文别名
——
英文名称
N-(thiophen-2-ylmethyl)hexanamide
英文别名
——
N-(thiophen-2-ylmethyl)hexanamide化学式
CAS
——
化学式
C11H17NOS
mdl
——
分子量
211.33
InChiKey
MJPMGQAXNXKJFW-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):
    2.7
  • 重原子数:
    14
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    57.3
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • beta-sheet mimetics and composition and methods relating thereto
    申请人:Myriad Pharmaceuticals, Inc.
    公开号:US20040014763A1
    公开(公告)日:2004-01-22
    Compounds having the following structure: 1 including pharmaceutically acceptable salts and stereoisomers thereof, wherein A, A′, B, X, Y, R 2 , R 3 , R 4 and R 5 are as defined herein. Such compounds have utility over a wide range of applications, including use as diagnostic and therapeutic agents. In particular, compounds of this invention, and pharmaceutical compositions containing such compounds, are tryptase antagonists.
    具有以下结构的化合物:1,包括药用可接受的盐及其立体异构体,其中A、A'、B、X、Y、R2、R3、R4和R5如本文所定义。这些化合物在广泛的应用范围内具有实用性,包括用作诊断和治疗剂。特别是,本发明的化合物和含有这些化合物的药物组合物是色胺酸蛋白酶抑制剂。
  • AGONISTS THAT ENHANCED BINDING OF INTEGRIN-EXPRESSING CELLS TO INTEGRIN RECEPTORS
    申请人:TEXAS HEART INSTITUTE
    公开号:US20150368234A1
    公开(公告)日:2015-12-24
    A method of enhancing binding of cells to an integrin-binding ligand comprises treating integrin-expressing cells in vitro with an agonist of integrin, wherein the integrin is selected from the group consisting of α4β1, α5β1, α4β7, αvβ3 and αLβ2, and contacting the treated cells with an integrin-binding ligand; integrin agonist compounds having the general formula I; methods of treating integrin-expressing cells with such agonists to enhance binding; and therapeutic methods comprising administering agonist-treated cells or agonist compounds to a mammal.
    一种增强细胞与整合素结合配体结合的方法包括在体外用整合素激动剂处理表达整合素的细胞,其中整合素被选择自α4β1、α5β1、α4β7、αvβ3和αLβ2组成的群体中的一种,并将处理后的细胞与整合素结合配体接触;具有一般式I的整合素激动剂化合物;用这样的激动剂处理表达整合素的细胞以增强结合的方法;以及包括向哺乳动物施用经激动剂处理的细胞或激动剂化合物的治疗方法。
  • Agonists that enhanced binding of integrin-expressing cells to integrin receptors
    申请人:TEXAS HEART INSTITUTE
    公开号:US10071980B2
    公开(公告)日:2018-09-11
    A method of enhancing binding of cells to an integrin-binding ligand comprises treating integrin-expressing cells in vitro with an agonist of integrin, wherein the integrin is selected from the group consisting of α4β1, α5β1, α4β7, αvβ3 and αLβ2, and contacting the treated cells with an integrin-binding ligand; integrin agonist compounds having the general formula I; methods of treating integrin-expressing cells with such agonists to enhance binding; and therapeutic methods comprising administering agonist-treated cells or agonist compounds to a mammal.
    一种增强细胞与整合素结合配体结合的方法,包括在体外用整合素的激动剂处理表达整合素的细胞,其中整合素选自由α4β1、α5β1、α4β7、αvβ3和αLβ2组成的组,并使处理过的细胞与整合素结合配体接触;具有通式Ⅰ的整合素激动剂化合物;用这种激动剂处理整合素表达细胞以增强结合的方法;以及治疗方法,包括给哺乳动物施用激动剂处理过的细胞或激动剂化合物。
  • Agonists that enhance binding of integrin-expressing cells to integrin receptors
    申请人:TEXAS HEART INSTITUTE
    公开号:US10287264B2
    公开(公告)日:2019-05-14
    A method of enhancing binding of cells to an integrin-binding ligand comprises treating integrin-expressing cells in vitro with an agonist of integrin, wherein the integrin is selected from the group consisting of α4β1, α5β1, α4β7, αvβ3 and αLβ2, and contacting the treated cells with an integrin-binding ligand; integrin agonist compounds having the general formula I; methods of treating integrin-expressing cells with such agonists to enhance binding; and therapeutic methods comprising administering agonist-treated cells or agonist compounds to a mammal.
    一种增强细胞与整合素结合配体结合的方法,包括在体外用整合素的激动剂处理表达整合素的细胞,其中整合素选自由α4β1、α5β1、α4β7、αvβ3和αLβ2组成的组,并使处理过的细胞与整合素结合配体接触;具有通式Ⅰ的整合素激动剂化合物;用这种激动剂处理整合素表达细胞以增强结合的方法;以及治疗方法,包括给哺乳动物施用激动剂处理过的细胞或激动剂化合物。
  • Compositions and methods for immunotherapies comprising small molecule integrin receptor-ligand agonist adjuvants
    申请人:7 Hills Interests LLC
    公开号:US10342866B2
    公开(公告)日:2019-07-09
    Small molecule integrin ligand mimetics facilitate integrin-ligand interactions, which may be used to prepare vaccines, adoptive cell therapies, immunotherapies for cancer, and a variety of other conditions. As integrin mediated cell-cell interactions are critical to antigen presentation and effector cell killing, increasing the efficiency of integrin receptor-ligand interactions will stabilize the immune synapse and improve effector functions. Compositions and methods including the mimetics enhance: (1) the priming of vaccines (including, but not limited to, cancer vaccines); (2) cytolytic activity of adoptive cell therapies (including, but not limited to γδT-cells, CTLs, NK, iNKT); (3) immunotherapies (including, but not limited to, negative checkpoint blockage strategies such as anti-CTLA-4 and anti-PD-1); and (4) biologic therapies (including, but not limited, to trastuzumab and rituxamab), whereby the mechanism-of-action includes antibody dependent cellular cytotoxicity (ADCC).
    小分子整合素配体模拟物能促进整合素与配体之间的相互作用,可用于制备疫苗、采用性细胞疗法、癌症免疫疗法以及其他多种治疗方法。由于整合素介导的细胞-细胞相互作用对于抗原递呈和效应细胞杀伤至关重要,因此提高整合素受体-配体相互作用的效率将稳定免疫突触并改善效应功能。包括模拟物在内的组合物和方法可提高(1) 疫苗(包括但不限于癌症疫苗)的启动;(2) 接种细胞疗法(包括但不限于γδT 细胞、CTL、NK、iNKT)的细胞溶解活性;(3) 免疫疗法(包括但不限于阴性检查点阻断策略,如抗 CTLA-4 和抗 PD-1);以及 (4) 生物疗法(包括但不限于曲妥珠单抗和利妥昔单抗),其作用机制包括抗体依赖性细胞毒性(ADCC)。
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