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Butyl(thiophen-2-ylmethyl)carbamic acid

中文名称
——
中文别名
——
英文名称
Butyl(thiophen-2-ylmethyl)carbamic acid
英文别名
butyl(thiophen-2-ylmethyl)carbamic acid
Butyl(thiophen-2-ylmethyl)carbamic acid化学式
CAS
——
化学式
C10H15NO2S
mdl
——
分子量
213.3
InChiKey
AIRBJINEBYGVJZ-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):
    2.3
  • 重原子数:
    14
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    68.8
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • AGONISTS THAT ENHANCE BINDING OF INTEGRIN-EXPRESSING CELLS TO INTEGRIN RECEPTORS
    申请人:Texas Heart Institute
    公开号:EP2640721B1
    公开(公告)日:2018-06-06
  • Agonists that enhance binding of integrin-expressing cells to integrin receptors
    申请人:Texas Heart Institute
    公开号:EP2881393B1
    公开(公告)日:2018-06-06
  • NOVEL COMPOSITIONS AND METHODS FOR IMMUNOTHERAPIES COMPRISING SMALL MOLECULE INTEGRIN RECEPTOR-LIGAND AGONIST ADJUVANTS
    申请人:7 HILLS INTERESTS, LLC
    公开号:EP3288585A2
    公开(公告)日:2018-03-07
  • [EN] NOVEL COMPOSITIONS AND METHODS FOR IMMUNOTHERAPIES COMPRISING SMALL MOLECULE INTEGRIN RECEPTOR-LIGAND AGONIST ADJUVANTS<br/>[FR] NOUVELLES COMPOSITIONS ET MÉTHODES POUR IMMUNOTHÉRAPIES COMPRENANT DES ADJUVANTS AGONISTES DES RÉCEPTEURS-LIGANDS D'INTÉGRINE À PETITES MOLÉCULES
    申请人:7 HILLS INTERESTS LLC
    公开号:WO2016176400A2
    公开(公告)日:2016-11-03
    Small molecule integrin ligand mimetics facilitate integrin-ligand interactions, which maybe 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 ϒδΤ-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).
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