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4-amino-3,3-dimethylbutanol | 622865-33-2

中文名称
——
中文别名
——
英文名称
4-amino-3,3-dimethylbutanol
英文别名
4-amino-3,3-dimethyl-butan-1-ol;4-Amino-3,3-dimethylbutan-1-ol
4-amino-3,3-dimethylbutanol化学式
CAS
622865-33-2
化学式
C6H15NO
mdl
MFCD19206192
分子量
117.191
InChiKey
INBMMXYCODJFAA-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

物化性质

  • 沸点:
    182.7±23.0 °C(Predicted)
  • 密度:
    0.909±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.1
  • 重原子数:
    8
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    46.2
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • P38ALPHA MITOGEN-ACTIVATED PROTEIN KINASE INHIBITORS
    申请人:GEN1E LIFESCIENCES INC.
    公开号:US20210355135A1
    公开(公告)日:2021-11-18
    Disclosed herein are p38α mitogen-activated protein kinase inhibitors, pharmaceutical compositions thereof, and therapeutic methods of using the p38α mitogen-activated protein kinase inhibitors.
    本文披露了p38α丝裂原活化蛋白激酶抑制剂、其药物组成物,以及利用p38α丝裂原活化蛋白激酶抑制剂的治疗方法。
  • Cellular accumulation of phosphonate analogs of hiv protease inhibitor compounds
    申请人:Arimilli N. Murty
    公开号:US20070010489A1
    公开(公告)日:2007-01-11
    Phosphonate substituted compounds with HIV protease inhibitory properties having use as therapeutics and for other industrial purposes are disclosed. The compositions inhibit 5 HIV protease activity and/or are useful therapeutically for the treatment of AIDS and other antiviral infections, as well as in assays for the detection of HIV protease.
    本发明揭示了具有HIV蛋白酶抑制剂性质的膦酸酯取代化合物,其具有作为治疗剂和其他工业用途的用途。该组合物抑制5型HIV蛋白酶活性和/或在治疗艾滋病和其他抗病毒感染方面具有治疗作用,以及在检测HIV蛋白酶方面的检测中有用。
  • Method and compositions for identifying anti-hiv therapeutic compounds
    申请人:Birkus Gabriel
    公开号:US20070190523A1
    公开(公告)日:2007-08-16
    The invention relates to methods and compositions for identifying compounds having therapeutic activity against human immunodeficiency virus (HIV).
    本发明涉及用于鉴定具有治疗人类免疫缺陷病毒(HIV)活性的化合物的方法和组合物。
  • CHIRAL CONTROL
    申请人:WAVE LIFE SCIENCES PTE. LTD.
    公开号:US20150211006A1
    公开(公告)日:2015-07-30
    The present invention relates to chirally controlled oligonucleotides, chirally controlled oligonucleotide compositions, and the method of making and using the same. The invention specifically encompasses the identification of the source of certain problems with prior methodologies for preparing chiral oligonucleotides, including problems that prohibit preparation of fully chirally controlled compositions, particularly compositions comprising a plurality of oligonucleotide types. In some embodiments, the present invention provides chirally controlled oligonucleotide compositions. In some embodiments, the present invention provides methods of making chirally controlled oligonucleotides and chirally controlled oligonucleotide compositions.
    本发明涉及手性控制的寡核苷酸、手性控制的寡核苷酸组合物以及其制备和使用方法。本发明特别涵盖了鉴定以前制备手性寡核苷酸方法中某些问题的来源,包括禁止制备完全手性控制的组合物,特别是包含多种寡核苷酸类型的组合物。在某些实施例中,本发明提供了手性控制的寡核苷酸组合物。在某些实施例中,本发明提供了制备手性控制的寡核苷酸和手性控制的寡核苷酸组合物的方法。
  • Chiral control
    申请人:WAVE LIFE SCIENCES LTD.
    公开号:US10590413B2
    公开(公告)日:2020-03-17
    The present invention relates to chirally controlled oligonucleotides, chirally controlled oligonucleotide compositions, and the method of making and using the same. The invention specifically encompasses the identification of the source of certain problems with prior methodologies for preparing chiral oligonucleotides, including problems that prohibit preparation of fully chirally controlled compositions, particularly compositions comprising a plurality of oligonucleotide types. In some embodiments, the present invention provides chirally controlled oligonucleotide compositions. In some embodiments, the present invention provides methods of making chirally controlled oligonucleotides and chirally controlled oligonucleotide compositions.
    本发明涉及手性受控寡核苷酸、手性受控寡核苷酸组合物以及制作和使用方法。本发明具体包括确定先前制备手性寡核苷酸方法中某些问题的根源,包括禁止制备完全手性控制的组合物,特别是包含多种寡核苷酸类型的组合物的问题。在某些实施方案中,本发明提供了手性控制的寡核苷酸组合物。在一些实施方案中,本发明提供了制作手性控制寡核苷酸和手性控制寡核苷酸组合物的方法。
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