4(1H)-Quinolinone, 8-chloro-2-[(2,4-dichlorophenyl)amino]-3-(3-methyl-1-oxobutyl)-5-nitro-
- Product Name
- 4(1H)-Quinolinone, 8-chloro-2-[(2,4-dichlorophenyl)amino]-3-(3-methyl-1-oxobutyl)-5-nitro-
- CAS No.
- 1361227-90-8
- Chemical Name
- 4(1H)-Quinolinone, 8-chloro-2-[(2,4-dichlorophenyl)amino]-3-(3-methyl-1-oxobutyl)-5-nitro-
- Synonyms
- JH-RE-06;JH-RE-06 ,S8850;JH-RE-06, 10 mM in DMSO;JH RE 06,DNA/RNA Synthesis,inhibit,Inhibitor,JHRE06;8-Chloro-2-((2,4-dichlorophenyl)amino)-3-(3-methylbutanoyl)-5-nitroquinolin-4(1H)-one;4(1H)-Quinolinone, 8-chloro-2-[(2,4-dichlorophenyl)amino]-3-(3-methyl-1-oxobutyl)-5-nitro-
- CBNumber
- CB45486742
- Molecular Formula
- C20H16Cl3N3O4
- Formula Weight
- 468.72
- MOL File
- 1361227-90-8.mol
4(1H)-Quinolinone, 8-chloro-2-[(2,4-dichlorophenyl)amino]-3-(3-methyl-1-oxobutyl)-5-nitro- Property
- Boiling point:
- 586.9±50.0 °C(Predicted)
- Density
- 1.503±0.06 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMSO: 5 mg/mL (10.67 mM)
- form
- Solid
- pka
- -3.78±0.70(Predicted)
- color
- White to yellow
N-Bromosuccinimide Price
- Product number
- SML2993
- Product name
- JH-RE-06
- Purity
- ≥98% (HPLC)
- Packaging
- 5MG
- Price
- $120.65
- Updated
- 2025/07/31
- Product number
- SML2993
- Product name
- JH-RE-06
- Purity
- ≥98% (HPLC)
- Packaging
- 25MG
- Price
- $489
- Updated
- 2025/07/31
- Product number
- CS-0099826
- Product name
- JH-RE-06
- Purity
- 99.87%
- Packaging
- 5mg
- Price
- $570
- Updated
- 2021/12/16
- Product number
- CS-0099826
- Product name
- JH-RE-06
- Purity
- 99.87%
- Packaging
- 10mg
- Price
- $965
- Updated
- 2021/12/16
- Product number
- Axon3002
- Product name
- JH-RE-06
- Purity
- 99%
- Packaging
- 5mg
- Price
- $159.5
- Updated
- 2021/12/16
4(1H)-Quinolinone, 8-chloro-2-[(2,4-dichlorophenyl)amino]-3-(3-methyl-1-oxobutyl)-5-nitro- Chemical Properties,Usage,Production
Uses
JH-RE-06-d6 is deuterium labele JH-RE-06. JH-RE-06, a potent REV1-REV7 interface inhibitor (IC50=0.78 μM; Ki=0.42 μM), targets REV1 that interacts with the REV7 subunit of POLζ. JH-RE-06 disrupts mutagenic translesion synthesis (TLS) by preventing recruitment of mutagenic POLζ. JH-RE-06 improves chemotherapy[1].
Biological Activity
JH-RE-06 is a potent and selective inhibitor of REV1-REV7 interaction th at induces REV1 dimerization blocking the REV1-REV7 interaction and POL ϲ recruitment. JH-RE-06 potently inhibits translesion synthesis (TLS) and augments cisplatin effectiveness in cultured human and mouse cell lines. It improves effectiveness of cisplatin in A375 tumor xenograft mouse model.
References
[1] Wojtaszek JL, et al. A Small Molecule Targeting Mutagenic Translesion Synthesis Improves Chemotherapy. Cell. 2019;178(1):152-159.e11. DOI:10.1016/j.cell.2019.05.028
4(1H)-Quinolinone, 8-chloro-2-[(2,4-dichlorophenyl)amino]-3-(3-methyl-1-oxobutyl)-5-nitro- Preparation Products And Raw materials
Raw materials
Preparation Products
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