Maximum quantity allowed is 999
请选择数量
CAS RN: 14892-97-8 | 产品编码: C3577
SCR7 Pyrazine

产品编码 | C3577 |
纯度/分析方法 ![]() |
>98.0%(HPLC) |
分子式/分子量 | C__1__8H__1__2N__4OS = 332.38 |
外观与形状(20°C) | 固体 |
储存温度 ![]() |
冷藏 (0-10°C) |
应避免的情况 | 加热 |
包装和容器 ![]() |
10MG-Glass Bottle with Plastic Insert (查看图片), 50MG-Glass Bottle with Plastic Insert (查看图片) |
CAS RN | 14892-97-8 |
Reaxys-RN | 306520 |
PubChem物质ID | 468591173 |
MDL编号 | MFCD02167478 |
技术规格
Appearance | White to Yellow to Green powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Melting point | 207.0 to 211.0 °C |
Elemental analysis(Nitrogen) | 16.00 to 17.50 % |
NMR | confirm to structure |
物性(参考值)
熔点 | 209 °C |
最大吸收波长 | 380 nm |
GHS
相关法规
运输信息
HS编码* | 2933.99-000 |
应用
CRISPR Genome Editing
SCR7 Pyrazine enhances CRISPR-mediated homology-directed repair (HDR) efficiency.
References
- Increasing the efficiency of CRISPR/Cas9-mediated precise genome editing of HSV-1 virus in human cells
应用
DNA Ligase Inhibitor: SCR7 Pyrazine
References
- CRISPR-Cas systems for editing, regulating and targeting genomes
- Increasing the efficiency of precise genome editing with CRISPR-Cas9 by inhibition of nonhomologous end joining
- Increasing the efficiency of homology-directed repair for CRISPR-Cas9-induced precise gene editing in mammalian cells
- An Inhibitor of Nonhomologous End-Joining Abrogates Double-Strand Break Repair and Impedes Cancer Progression
- SCR7 is neither a selective nor a potent inhibitor of human DNA ligase IV
- Synthesis and structure determination of SCR7, a DNA ligase inhibitor
- Autocyclized and oxidized forms of SCR7 induce cancer cell death by inhibiting nonhomologous DNA end joining in a Ligase IV dependent manner
- Water-soluble version of SCR7-pyrazine inhibits DNA repair and abrogates tumor cell proliferation
文档
产品文档 (部分产品的分析图谱无法提供,敬请谅解。)
化学品安全说明书(SDS)
请选择语言。
如需更多帮助,请联系我 们。
技术规格
CoA及其他文档
请输入批号
批号输入有误。请输入中横线前的4-5个字母数字字符。
示例 CoA
可下载CoA示例。注:该示例不一定是最新批次的CoA。
目前没有该产品的 CoA 示例。
分析图谱
请输入批号
批号输入有误。请输入中横线前的4-5个字母数字字符。
很抱歉,您搜索的分析图谱无法提供。