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4-amino-6-ethyl-8-methyl-1H-quinazolin-2-one

中文名称
——
中文别名
——
英文名称
4-amino-6-ethyl-8-methyl-1H-quinazolin-2-one
英文别名
——
4-amino-6-ethyl-8-methyl-1H-quinazolin-2-one化学式
CAS
——
化学式
C11H13N3O
mdl
——
分子量
203.24
InChiKey
HTYOMBSEPSFCPX-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):
    1.3
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    67.5
  • 氢给体数:
    2
  • 氢受体数:
    1

文献信息

  • OLIGONUCLEOTIDES FOR TREATING EXPANDED REPEAT DISEASES
    申请人:Sarepta Therapeutics, Inc.
    公开号:EP2785729B1
    公开(公告)日:2020-11-04
  • [EN] OLIGONUCLEOTIDE COMPOSITIONS AND METHODS THEREOF<br/>[FR] COMPOSITIONS D'OLIGONUCLÉOTIDES ET PROCÉDÉS ASSOCIÉS
    申请人:WAVE LIFE SCIENCES LTD
    公开号:WO2017062862A2
    公开(公告)日:2017-04-13
    Among other things, the present disclosure relates to designed oligonucleotides, compositions, and methods thereof. In some embodiments, provided oligonucleotide compositions provide altered splicing of a transcript. In some embodiments, provided oligonucleotide compositions have low toxicity. In some embodiments, provided oligonucleotide compositions provide improved protein binding profiles. In some embodiments, provided oligonucleotide compositions have improved delivery. In some embodiments, provided oligonucleotide compositions have improved uptake. In some embodiments, the present disclosure provides methods for treatment of diseases using provided oligonucleotide compositions.
  • [EN] COMPOSITIONS COMPRISING EXON SKIPPING OLIGONUCLEOTIDE CONJUGATES FOR TREATING MUSCULAR DYSTROPHY<br/>[FR] COMPOSITIONS COMPRENANT DES CONJUGUÉS D'OLIGONUCLÉOTIDES À SAUT D'EXON POUR LE TRAITEMENT DE LA DYSTROPHIE MUSCULAIRE
    申请人:[en]SAREPTA THERAPEUTICS, INC.
    公开号:WO2022140535A1
    公开(公告)日:2022-06-30
    Composition comprising: (a) an antisense oligonucleotide conjugate comprising a cell penetrating peptide covalently attached to a nucleic acid analog, or a pharmaceutically acceptable salt thereof, wherein the cell penetrating peptide includes at least two positively charged amino acids; (b) one or more surfactants; (c) one or more sugars; and (d) one or more buffering agents are provided herein.
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