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N,N,N,N-tetra(2-thienylmethyl)-2,6-pyridinedicarboxamide | 1378535-12-6

中文名称
——
中文别名
——
英文名称
N,N,N,N-tetra(2-thienylmethyl)-2,6-pyridinedicarboxamide
英文别名
N,N,N',N'-tetrakis(2-thienylmethyl)pyridine-2,6-dicarboxamide;2-N,2-N,6-N,6-N-tetrakis(thiophen-2-ylmethyl)pyridine-2,6-dicarboxamide
N,N,N,N-tetra(2-thienylmethyl)-2,6-pyridinedicarboxamide化学式
CAS
1378535-12-6
化学式
C27H23N3O2S4
mdl
——
分子量
549.763
InChiKey
IVBBJDFNLLFWLO-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):
    5.3
  • 重原子数:
    36
  • 可旋转键数:
    10
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    167
  • 氢给体数:
    0
  • 氢受体数:
    7

文献信息

  • AGONISTS THAT ENHANCE BINDING OF INTEGRIN-EXPRESSING CELLS TO INTEGRIN RECEPTORS
    申请人:Biediger Ronald J.
    公开号:US20130236434A1
    公开(公告)日:2013-09-12
    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的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,其中整合素选自α4β1、α5β1、α4β7、αvβ3和αLβ2群,然后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;使用这种激动剂治疗表达整合素的细胞以增强结合的方法;以及包括将激动剂处理的细胞或激动剂化合物给哺乳动物的治疗方法。
  • AGONISTS THAT ENHANCED BINDING OF INTEGRIN-EXPRESSING CELLS TO INTEGRIN RECEPTORS
    申请人:TEXAS HEART INSTITUTE
    公开号: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。
  • INTEGRIN AGONISTS OR ACTIVATING COMPOUNDS AND METHODS FOR MAKING AND USING SAME
    申请人:7 Hills Pharma LLC
    公开号:US20220118086A1
    公开(公告)日:2022-04-21
    Small molecule integrin agonists or integrin activating compounds including at least one di-alkylaryl amine end group and at least one alkyl or alkenoxy linking group including at least one protonatable moiety, wherein the compounds enhance vaccine efficacies, enhance adoptive cell therapy efficacies, enhance immunotherapy efficacies, enhance therapeutic antibody therapy efficacies, enhance checkpoint inhibitor therapy efficacies, enhance effector cell therapy efficacies, and enhanced cell based transplant efficacies and wherein at protonatable moiety either protonate at biological pHs or bears a charge with associated pharmaceutically acceptable counterion making the compound water soluble to improve bioavailability and methods for making and using same.
    小分子整合素激动剂或整合素活化化合物,包括至少一个二烷基芳基胺末端基团和至少一个烷基或烯氧基连接基团,其中包括至少一个可质子化基团,这些化合物增强疫苗效力、增强养护细胞治疗效力、增强免疫疗法效力、增强治疗性抗体疗法效力、增强检查点抑制剂疗法效力、增强效应细胞治疗效力以及增强基于细胞的移植效力。其中,可质子化基团在生物pH下质子化或带有相关的医药可接受的对离子,使化合物溶性以提高生物利用度,并提供制备和使用的方法。
  • Agonists that enhance binding of integrin-expressing cells to integrin receptors
    申请人:Texas Heart Institute
    公开号:EP2881392A1
    公开(公告)日:2015-06-10
    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 enhanced binding of integrin-expressing cells to integrin receptors
    申请人:TEXAS HEART INSTITUTE
    公开号:US10035784B2
    公开(公告)日:2018-07-31
    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。
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