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N-(5-methyl-6-oxoheptyl)-5-(1,2,3,4,6-pentahydroxyhexoxy)pentanamide

中文名称
——
中文别名
——
英文名称
N-(5-methyl-6-oxoheptyl)-5-(1,2,3,4,6-pentahydroxyhexoxy)pentanamide
英文别名
——
N-(5-methyl-6-oxoheptyl)-5-(1,2,3,4,6-pentahydroxyhexoxy)pentanamide化学式
CAS
——
化学式
C19H37NO8
mdl
——
分子量
407.5
InChiKey
OOWICLKMUXOYNO-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):
    -1.4
  • 重原子数:
    28
  • 可旋转键数:
    17
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    157
  • 氢给体数:
    6
  • 氢受体数:
    8

文献信息

  • COMPLEMENT COMPONENT C5 iRNA COMPOSITIONS AND METHODS OF USE THEREOF
    申请人:Alnylam Pharmaceuticals, Inc.
    公开号:US20150247143A1
    公开(公告)日:2015-09-03
    The invention relates to iRNA, e.g., double-stranded ribonucleic acid (dsRNA), compositions targeting the complement component C5 gene, and methods of using such iRNA, e.g., dsRNA, compositions to inhibit expression of C5 and to treat subjects having a complement component C5-associated disease, e.g., paroxysmal nocturnal hemoglobinuria.
    该发明涉及iRNA,例如双链核糖核酸(dsRNA),针对补体成分C5基因的组合物,以及使用这种iRNA,例如dsRNA,组合物来抑制C5的表达并治疗患有补体成分C5相关疾病的受试者,例如周期性夜间血红蛋白尿。
  • Compositions and Methods for Inhibition of Expression of Protein C (PROC) Genes
    申请人:Toudjarska Ivanka
    公开号:US20140142162A1
    公开(公告)日:2014-05-22
    The invention relates to double-stranded ribonucleic acid (dsRNA) targeting a PROC gene, and methods of using the dsRNA to inhibit expression of PROC. At least one nucleotide of the dsRNA can be a modified nucleotide, e.g., a 2-0-methyl modified nucleotide, a nucleotide comprising a 5′-phosphorothioate group, and a terminal nucleotide linked to a cholesteryl derivative or dodecanoic acid bisdecylamide group. Other examples of modified nucleotides include a 2′-deoxy-2′-fluoro modified nucleotide, a 2′-deoxymodified nucleotide, a locked nucleotide, an abasic nucleotide, 2′-amino-modified nucleotide, 2′-alkyl-modified nucleotide, morpholino nucleotide, a phosphoramidate, and a non-natural base comprising nucleotide. A dsRNA of the invention can include one or more of any of these modified nucleotides.
  • Compositions and methods for inhibiting hepcidin antimicrobial peptide (HAMP) or HAMP-related gene expression
    申请人:Alnylam Pharmaceuticals, Inc.
    公开号:US20160186172A1
    公开(公告)日:2016-06-30
    The invention relates to lipid formulated double-stranded ribonucleic acid (dsRNA) targeting a hepcidin antimicrobial peptide (HAMP) and/or HAMP-related gene, and methods of using the dsRNA to inhibit expression of HAMP and/or HAMP-related genes.
  • US9249415B2
    申请人:——
    公开号:US9249415B2
    公开(公告)日:2016-02-02
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