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1-(1-Benzyl-2,5-dimethylpyrrol-3-yl)-2-(1-methyltetrazol-5-yl)sulfanylethanone

中文名称
——
中文别名
——
英文名称
1-(1-Benzyl-2,5-dimethylpyrrol-3-yl)-2-(1-methyltetrazol-5-yl)sulfanylethanone
英文别名
——
1-(1-Benzyl-2,5-dimethylpyrrol-3-yl)-2-(1-methyltetrazol-5-yl)sulfanylethanone化学式
CAS
——
化学式
C17H19N5OS
mdl
——
分子量
341.4
InChiKey
AHPQZCDAMIJFNI-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):
    3
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    90.9
  • 氢给体数:
    0
  • 氢受体数:
    5

文献信息

  • PHARMACEUTICAL COMPOSITION INCLUDING MIGRATORY FACTOR FOR GUIDING PLURIPOTENT STEM CELLS TO INJURY
    申请人:Clio, Inc.
    公开号:EP2962698A1
    公开(公告)日:2016-01-06
    The purpose of the present invention is to identify a migratory factor that guides pluripotent stem cells (Muse cells) useful in new medical applications to damage, and to provide a pharmaceutical composition that includes the migratory factor for promoting tissue regeneration in regenerative medicine that makes use of Muse cells. In the present invention, a receptor that is specifically expressed in Muse cells rather than non-Muse cells was identified, and it was confirmed that a ligand for this receptor can function as a migratory factor. In the present invention, sphingosine-1-phosphate (S1P) was identified as a migratory factor, and thus, the present invention pertains to a pharmaceutical composition for guiding pluripotent stem cells to damage, the composition including SIP as an active ingredient.
    本发明的目的是鉴定一种可引导多能干细胞(缪斯细胞)在新的医疗应用中发挥作用的迁移因子,并提供一种包含该迁移因子的药物组合物,用于促进再生医学中利用缪斯细胞的组织再生。在本发明中,确定了一种在缪斯细胞而非非缪斯细胞中特异表达的受体,并证实该受体的配体可作为迁移因子发挥作用。在本发明中,鞘氨醇-1-磷酸(S1P)被确定为一种迁移因子,因此,本发明涉及一种用于引导多能干细胞受损的药物组合物,该组合物包括作为活性成分的SIP。
  • Pharmaceutical composition including migratory factor for guiding pluripotent stem cells to damage
    申请人:CLIO, INC.
    公开号:US10034889B2
    公开(公告)日:2018-07-31
    The purpose of the present invention is to identify a migratory factor that guides pluripotent stem cells (Muse cells) useful in new medical applications to damage, and to provide a pharmaceutical composition that includes the migratory factor for promoting tissue regeneration in regenerative medicine that makes use of Muse cells. In the present invention, a receptor that is specifically expressed in Muse cells rather than non-Muse cells was identified, and it was confirmed that a ligand for this receptor can function as a migratory factor. In the present invention, sphingosine-1-phosphate (S1P) was identified as a migratory factor, and thus, the present invention pertains to a pharmaceutical composition for guiding pluripotent stem cells to damage, the composition including S1P as an active ingredient.
    本发明的目的是鉴定一种可引导多能干细胞(缪斯细胞)在新的医疗应用中发挥作用的迁移因子,并提供一种包含该迁移因子的药物组合物,用于促进再生医学中利用缪斯细胞的组织再生。在本发明中,确定了一种在缪斯细胞而非非缪斯细胞中特异表达的受体,并证实该受体的配体可作为迁移因子发挥作用。在本发明中,鞘氨醇-1-磷酸(S1P)被确定为一种迁移因子,因此,本发明涉及一种引导多能干细胞受损的药物组合物,该组合物包括作为活性成分的S1P。
  • PHARMACEUTICAL COMPOSITION INCLUDING MIGRATORY FACTOR FOR GUIDING PLURIPOTENT STEM CELLS TO DAMAGE
    申请人:CLIO INC.
    公开号:US20160354393A1
    公开(公告)日:2016-12-08
    The purpose of the present invention is to identify a migratory factor that guides pluripotent stem cells (Muse cells) useful in new medical applications to damage, and to provide a pharmaceutical composition that includes the migratory factor for promoting tissue regeneration in regenerative medicine that makes use of Muse cells. In the present invention, a receptor that is specifically expressed in Muse cells rather than non-Muse cells was identified, and it was confirmed that a ligand for this receptor can function as a migratory factor. In the present invention, sphingosine-1-phosphate (S1P) was identified as a migratory factor, and thus, the present invention pertains to a pharmaceutical composition for guiding pluripotent stem cells to damage, the composition including S1P as an active ingredient.
  • US9446033B2
    申请人:——
    公开号:US9446033B2
    公开(公告)日:2016-09-20
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