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3-<4-Chlor-phenylmercapto>-propionsaeure-chlorid | 67141-35-9

中文名称
——
中文别名
——
英文名称
3-<4-Chlor-phenylmercapto>-propionsaeure-chlorid
英文别名
3-(4-Chlorophenyl)sulfanylpropanoyl chloride;3-(4-chlorophenyl)sulfanylpropanoyl chloride
3-<4-Chlor-phenylmercapto>-propionsaeure-chlorid化学式
CAS
67141-35-9
化学式
C9H8Cl2OS
mdl
——
分子量
235.134
InChiKey
SEOZBIRKHDPZMI-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:
    323.8±27.0 °C(Predicted)
  • 密度:
    1.35±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    42.4
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Pagani; Baruffini; Borgna, Farmaco, Edizione Scientifica, 1978, vol. 33, # 5, p. 332 - 349
    作者:Pagani、Baruffini、Borgna、Caccialanza
    DOI:——
    日期:——
  • INHIBITORS OF RNA-GUIDED NUCLEASES AND USES THEREOF
    申请人:The Brigham and Women's Hospital, Inc.
    公开号:US20240115557A1
    公开(公告)日:2024-04-11
    The need to control the activity and fidelity of CRISPR-associated nucleases has resulted in the demand for inhibitory anti-CRISPR molecules. Current small-molecule inhibitor discovery platforms are not generalizable to multiple nuclease classes, only target the initial step in the catalytic activity, and require high concentration of nuclease, resulting in inhibitors with suboptimal attributes, including poor potency. Herein, Applicants report a high-throughput discovery pipeline consisting of a FRET-based assay that is generalizable to contemporary and emerging nucleases, operates at low nuclease concentration, and targets all catalytic steps. Applicants applied this pipeline to identify BRD7586, a cell-permeable small-molecule inhibitor of SpCas9, that is 2-fold more potent than current inhibitors. Furthermore, unlike the reported inhibitors, BRD7586 enhanced SpCas9 specificity and its activity was independent of the genomic loci, DNA repair pathway, or mode of nuclease delivery. Overall, these studies describe a general pipeline to identify inhibitors of contemporary and emerging CRISPR-associated nucleases. Described herein are compositions and methods for inhibiting the activity of RNA-guided endonucleases, and methods for identifying such compositions.
  • Abdel-Wahab, Aboel-Magd A.; El-Khawaga, Ahmed M.; El-Zohry, Maher F., Phosphorus and Sulfur and the Related Elements, 1984, vol. 19, p. 31 - 44
    作者:Abdel-Wahab, Aboel-Magd A.、El-Khawaga, Ahmed M.、El-Zohry, Maher F.、Khalaf, Ali A.
    DOI:——
    日期:——
  • PONCI; BARUFFINI; BORGNA, Farmaco, Edizione Scientifica, 1964, vol. 19, p. 356 - 376
    作者:PONCI、BARUFFINI、BORGNA
    DOI:——
    日期:——
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