14892-97-8
14892-97-8
Chemical Structure
SCR7 pyrazine
- CAS No.: 14892-97-8
- Formula:C18H12N4OS
- Molecular Weight:332.38
IUPAC Name: 6,7-diphenyl-2-thioxo-2,3-dihydropteridin-4(1H)-one
InChIKey: GSRTWXVBHGOUBU-UHFFFAOYSA-N
SMILES: O=C1NC(NC2=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N=C12)=S
Biological Activity: SCR7 pyrazine is a DNA ligase IV inhibitor that blocks nonhomologous end-joining (NHEJ) in a ligase IV-dependent manner. SCR7 pyrazine increases the efficiency of Cas9-mediated homology-directed repair (HDR). SCR7 pyrazine induces cell apoptosis and has anticancer activity[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
SCR7 pyrazine | 99.88% | SCR7 pyrazine is a DNA ligase IV inhibitor that blocks nonhomologous end-joining (NHEJ) in a ligase IV-dependent manner. SCR7 pyrazine increases the efficiency of Cas9-mediated homology-directed repair (HDR). SCR7 pyrazine induces cell apoptosis and has anticancer activity. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
SCR7 pyrazine (Standard) | SCR7 pyrazine (Standard) is the analytical standard of SCR7 pyrazine (HY-107845). This product is intended for research and analytical applications. SCR7 pyrazine is a DNA ligase IV inhibitor that blocks nonhomologous end-joining (NHEJ) in a ligase IV-dependent manner. SCR7 pyrazine increases the efficiency of Cas9-mediated homology-directed repair (HDR). SCR7 pyrazine induces cell apoptosis and has anticancer activity. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
Structural Analogs
-
Similarity Score 0.60
HY-W8393832,3-Diphenylquinoxaline-6-sulphonamide -
Similarity Score 0.60
HY-W0287142,3-Diphenylquinoxaline-6-carboxylic acid -
Similarity Score 0.58
HY-79589R5-Chloro-2,3-diphenylpyrazine (Standard) -
Similarity Score 0.56
HY-182397ZX-J-19L -
Similarity Score 0.56
HY-W038396Ferrotrace -
Similarity Score 0.56
HY-W1124834-(4,5-Diphenyl-1H-imidazol-2-yl)pyridine -
Similarity Score 0.55
HY-W0087094-(4,5-Diphenyl-1H-imidazol-2-yl)phenol -
Similarity Score 0.55
HY-146805EB1 -
Similarity Score 0.55
HY-16034AKT-IN-20 -
Explore the MedChemAI to find more analogs
References
- [1]. Srivastava M, et al. An inhibitor of nonhomologous end-joining abrogates double-strand break repair and impedes cancer progression. Cell. 2012 Dec 21;151(7):1474-87. [Content Brief]
- [2]. Lin C, et al. Increasing the Efficiency of CRISPR/Cas9-mediated Precise Genome Editing of HSV-1 Virus in Human Cells. Sci Rep. 2016 Oct 7;6:34531. [Content Brief]
