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2-methyl-N-propylpentanamide

中文名称
——
中文别名
——
英文名称
2-methyl-N-propylpentanamide
英文别名
——
2-methyl-N-propylpentanamide化学式
CAS
——
化学式
C9H19NO
mdl
MFCD02860561
分子量
157.25
InChiKey
VTXPRRUQVKYCGX-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):
    2.4
  • 重原子数:
    11
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.888
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    1

文献信息

  • [EN] IN VIVO ENGINEERED CEREBLON PROTEIN<br/>[FR] PROTÉINE CEREBLON MODIFIÉE IN VIVO
    申请人:VIVIDION THERAPEUTICS INC
    公开号:WO2020140039A1
    公开(公告)日:2020-07-02
    Disclosed herein are in vivo engineered cereblon protein and methods of making the same. The in vivo engineered cereblon protein can include a site-specific non-naturally occurring modification at cysteine 287 as set forth in SEQ ID NO:1, or cysteine 286 as set forth in SEQ ID NO: 2 or 3, the modification comprising a moiety resulting from an in vivo Michael addition reaction between an exogenous Michael acceptor and the cysteine 287 as set forth in SEQ ID NO:1, or cysteine 286 as set forth in SEQ ID NO: 2 or 3.
    本公开揭示了体内工程的 cereblon 蛋白质及其制备方法。体内工程的 cereblon 蛋白质可以包括在胱酸 287 处进行的特异性非自然发生修饰,如 SEQ ID NO:1 中所述,或者在 SEQ ID NO:2 或 3 中所述的胱酸 286 处进行的修饰,该修饰包括由体内 Michael 加成反应中外源 Michael 受体和在 SEQ ID NO:1 中所述的胱酸 287,或者在 SEQ ID NO:2 或 3 中所述的胱酸 286 之间产生的基团。
  • Crosslinked Gels Comprising Polyalkyleneimines, And Their Uses As Medical Devices
    申请人:HyperBranch Medical Technology, Inc.
    公开号:US20210275718A1
    公开(公告)日:2021-09-09
    One aspect of the present invention generally relates to methods of sealing a wound or tissue plane or filling a void splace. In a preferred embodiment, the wound is an ophthalmic, pleural or dural wound. In certain instances, the compositions used to seal the wound or tissue plane comprises a polyalkyleneimine. In a preferred embodiment, the polyalkyleneimine is polyethyleneimine. Treatment of the polyethyleneimine with a cross-linking reagent causes the polyethyleneimine polymers to polymerize forming a seal. In certain instances, the cross-linking reagent is a polyethylene glycol having reactive terminal groups. In certain instances, the reactive terminal groups are activated esters, such as N-hydroxy succinimide ester. In certain instances, the reactive terminal groups are isocyanates. In certain instances, the polyethyleneimine has a lysine, cysteine, isocysteine or other nucleophilic group attached to the periphery of the polymer. In certain instances, the polyethyleneimine is mixed with a second polymer, such as a polyethylene glycol containing nucleophilic groups. In certain instances, the compositions used to seal the wound or tissue plane are formed by reacting a polyalkyleneimine bearing electrophilic groups with a cross-linking reagent containing nucleophilic groups. In certain instances, the electrophilic groups on the polyalkyleneimine are activated esters, such as N-hydroxy succinimide ester. In certain instances, the compositions used to seal the wound or tissue plane are formed by reacting a polyalkyleneimine bearing photopolymerizable groups with ultraviolet or visible light. Compositions used to seal the wound which contain PEI or a derivative of PEI are found to adhere tightly to the tissue. Other aspects of the present invention relate to methods of filling a void of a patient or adhering tissue. In certain instances, the methods use a polyalkyleneimine. In a preferred embodiment, the polyalkyleneimine is polyethyleneimine. Another aspect of the present invention relates to a polymeric composition formed by exposing a polyalkyleneimine to an activated polyalkylene glycol. In certain instances, the composition is attached to mammalian tissue.
  • US5224987A
    申请人:——
    公开号:US5224987A
    公开(公告)日:1993-07-06
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