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(2R,4R)-5-hydroxy-4-(hydroxymethyl)-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-10-one

中文名称
——
中文别名
——
英文名称
(2R,4R)-5-hydroxy-4-(hydroxymethyl)-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-10-one
英文别名
——
(2R,4R)-5-hydroxy-4-(hydroxymethyl)-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-10-one化学式
CAS
——
化学式
C9H10N2O5
mdl
——
分子量
226.19
InChiKey
UUGITDASWNOAGG-AYZDMWBASA-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):
    -2.5
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    91.6
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • EXTRAHEPATIC DELIVERY
    申请人:ALNYLAM PHARMACEUTICALS, INC.
    公开号:US20220125823A1
    公开(公告)日:2022-04-28
    The invention relates to a method of gene silencing, comprising administering to a cell or a subject in need thereof a therapeutically effective amount of the lipophilic moieties-conjugated double-stranded iRNAs at one or more internal positions on at least one strand, optionally via a linker or carrier.
    本发明涉及一种基因沉默方法,包括向细胞或需要治疗的受体中给予脂溶性基团偶联的双链iRNA,在至少一条链的一个或多个内部位置上给予治疗有效量,可选地通过连接剂或载体给予。
  • Nucleic Acid Labeling Compounds
    申请人:McGall Glenn
    公开号:US20110082289A1
    公开(公告)日:2011-04-07
    Nucleic acid labeling compounds are disclosed. The compounds are synthesized by condensing a heterocyclic derivative with a cyclic group (e.g. a ribofuranose derivative). The labeling compounds are suitable for enzymatic attachment to a nucleic acid, either terminally or internally, to provide a mechanism of nucleic acid detection.
  • Nucleic Acid Labelling Compounds
    申请人:McGall Glenn
    公开号:US20120053336A1
    公开(公告)日:2012-03-01
    Nucleic acid labeling compounds are disclosed. The compounds are synthesized by condensing a heterocyclic derivative with a cyclic group (e.g. a ribofuranose derivative). The labeling compounds are suitable for enzymatic attachment to a nucleic acid, either terminally or internally, to provide a mechanism of nucleic acid detection.
  • Novel 2'/3'/5'-(R/S)-Serinyl Functionalized Oligonucleotides
    申请人:COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH
    公开号:US20170044527A1
    公开(公告)日:2017-02-16
    The present invention provides novel chiral serinyl functionalized tethered oligunucleotides i.e. R/S serinyl functionalized tethered oligonucleotides and the process of preparation thereof. Specifically, the present invention provides a modified nucleoside unit containing the R/S serinyl derivative at 2′ of the sugar unit which is introduced in a nucleotide sequence. Also, capping of the oligonucleotides with abasic serinyl derivative to render the nuclease stability to the oligonucleotiedds is also disclosed. The chiral serinyl functionalized tethered oligonucleotides, 2′-O-[R/S-( 2 -amino- 3 -methoxy)propyl] nucleic acids with both ′3- and 5′-ends capped with two units of abasic serine have antisense activity against the miRNA.
  • Chemically Ligated RNAs for CRISPR/Cas9-lgRNA Complexes as Antiviral Therapeutic Agents
    申请人:Dr. Minghong Zhong
    公开号:US20210222165A1
    公开(公告)日:2021-07-22
    Provided herein are chemically ligated guide RNA oligonucleotides (lgRNA) which comprise two functional RNA modules (crgRNA and tracrgRNA) joined by non-nucleotide chemical linkers (nNt-linker), their complexes with CRISPR-Cas9, and cells comprising lgRNAs, preparation methods of Cas9-1gRNA complexes, and their uses for prevention and treatments of viral infections in humans. Also disclosed are processes and methods for preparation of these compounds.
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