90987-48-7

Basic information

• Product Name: Pyrimido[4,5-b]quinoline-2,4(3H,10H)-dione, 8-chloro-10-(4-chlorophenyl)-
• CAS NO: 90987-48-7
• Molecular Formula: C17H9Cl2N3O2
• Molecular Weight: 358.17800
• Mol File: 90987-48-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Pyrimido[4,5-b]quinoline-2,4(3H,10H)-dione, 8-chloro-10-(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrimido[4,5-b]quinoline-2,4(3H,10H)-dione, 8-chloro-10-(4-chlorophenyl)-(90987-48-7)
• EPA Substance Registry System: Pyrimido[4,5-b]quinoline-2,4(3H,10H)-dione, 8-chloro-10-(4-chlorophenyl)-(90987-48-7)

Safety Data

• Hazardous Substances Data: 90987-48-7(Hazardous Substances Data)

Upstream product

• 61072-56-8 4-chloro-2-fluorobenzaldehyde 
• 21333-02-8 6-(4-chlorophenylamino)-1H-pyrimidine-2,4-dione 
• 84459-33-6 2-bromo-4-chlorobenzaldehyde 
• 874-42-0 2,4-dichlorobenzaldeyhde 

Relevant articles and documents

5-Deazaflavin derivatives as inhibitors of p53 ubiquitination by HDM2

Based on previous reports of certain 5-deazaflavin derivatives being capable of activating the tumour suppressor p53 in cancer cells through inhibition of the p53-specific ubiquitin E3 ligase HDM2, we have conducted an structure-activity relationship (SAR) analysis through systematic modification of the 5-deazaflavin template. This analysis shows that HDM2-inhibitory activity depends on a combination of factors. The most active compounds (e.g., 15) contain a trifluoromethyl or chloro substituent at the deazaflavin C9 position and this activity depends to a large extent on the presence of at least one additional halogen or methyl substituent of the phenyl group at N10. Our SAR results, in combination with the HDM2 RING domain receptor recognition model we present, form the basis for the design of drug-like and potent activators of p53 for potential cancer therapy.