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Merck
CN

SML1546

Sigma-Aldrich

SCR7 吡嗪

≥98% (HPLC)

别名:

2,3-二氢-6,7-二苯基-2-硫代-4 (1H)-蝶啶酮, 6,7-二苯基-2-硫代-卢马嗪 (8CI)

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About This Item

经验公式(希尔记法):
C18H12N4OS
CAS号:
分子量:
332.38
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

质量水平

方案

≥98% (HPLC)

表单

powder

颜色

faintly yellow to dark yellow

溶解性

DMSO: 10 mg/mL, clear

储存温度

room temp

SMILES字符串

O=C(C1=C(N2)N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N1)NC2=S

InChI

1S/C18H12N4OS/c23-17-15-16(21-18(24)22-17)20-14(12-9-5-2-6-10-12)13(19-15)11-7-3-1-4-8-11/h1-10H,(H2,20,21,22,23,24)

InChI key

GSRTWXVBHGOUBU-UHFFFAOYSA-N

相关类别

一般描述

SCR7 吡嗪是 DNA 连接酶 IV 的抑制剂。

应用

SCR7 吡嗪已被用作非同源末端连接 (NHEJ) 调节剂,研究其对 CRISPR/Cas9 介导的编辑的影响。
SCR7 吡嗪已被证明可以增强 CRISPR 基因组编辑效率。要查看其他小分子 CRISPR 增强子,请访问 sigma.com/CRISPR-enhancers

生化/生理作用

据报道,SCR7 吡嗪是非同源末端连接 (NHEJ) 的抑制剂,并已被证明可增强 CRISPR-Cas9 基因组编辑的效率。
据报道,SCR7 吡嗪是非同源末端连接 (NHEJ) 的抑制剂,并已被证明可增强 CRISPR-Cas9 基因组编辑的效率。SCR7 吡嗪对 CRISPR 应用效率和靶向精度的影响已被证明是细胞类型特异性和上下文依赖性的。sr7 吡嗪是 sr7 自发环化的产物,由 Srivastava 等人首先报道。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

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访问文档库

Disruption of diphthamide synthesis genes and resulting toxin resistance as a robust technology for quantifying and optimizing CRISPR/Cas9-mediated gene editing.
Killian T, et al.
Scientific Reports, 7(1), 15480-15480 (2017)
Diane Yang et al.
Scientific reports, 6, 21264-21264 (2016-02-19)
Efficient gene editing is essential to fully utilize human pluripotent stem cells (hPSCs) in regenerative medicine. Custom endonuclease-based gene targeting involves two mechanisms of DNA repair: homology directed repair (HDR) and non-homologous end joining (NHEJ). HDR is the preferred mechanism
pRB-Depleted Pluripotent Stem Cell Retinal Organoids Recapitulate Cell State Transitions of Retinoblastoma Development and Suggest an Important Role for pRB in Retinal Cell Differentiation.
Rozanska, et al.
Stem Cells Translational Medicine, 11, 415-433 (2023)
Yuanwu Ma et al.
RNA biology, 13(7), 605-612 (2016-05-11)
Precise modifications such as site mutation, codon replacement, insertion or precise targeted deletion are needed for studies of accurate gene function. The CRISPR/Cas9 system has been proved as a powerful tool to generate gene knockout and knockin animals. But the
Justin Moser et al.
Proceedings of the National Academy of Sciences of the United States of America, 115(35), E8219-E8227 (2018-08-17)
The Restriction Point was originally defined as the moment that cells commit to the cell cycle and was later suggested to coincide with hyperphosphorylation of the retinoblastoma protein (Rb). Current cell cycle models posit that cells exit mitosis into a

商品

业内研究了CRISPR基因组编辑背景下的HDR调控,发现各种细胞类型中增强CRISPR介导的HDR效率的小分子。

Modulation of homology-directed repair (HDR) within the context of CRISPR-genome editing has led to the identification of small molecules that enhance CRISPR-mediated HDR efficiency in various cell types.

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