1224583-53-2

Basic information

• Product Name: 1-[3-acetyl-5-[(3,5-diacetyl-2,4,6-trihydroxyphenyl)-4-N,N-dimethyl-aminophenyl-methyl]-2,4,6-trihydroxyphenyl]ethanone
• CAS NO: 1224583-53-2
• Molecular Weight: 551.55
• Mol File: 1224583-53-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-[3-acetyl-5-[(3,5-diacetyl-2,4,6-trihydroxyphenyl)-4-N,N-dimethyl-aminophenyl-methyl]-2,4,6-trihydroxyphenyl]ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[3-acetyl-5-[(3,5-diacetyl-2,4,6-trihydroxyphenyl)-4-N,N-dimethyl-aminophenyl-methyl]-2,4,6-trihydroxyphenyl]ethanone(1224583-53-2)
• EPA Substance Registry System: 1-[3-acetyl-5-[(3,5-diacetyl-2,4,6-trihydroxyphenyl)-4-N,N-dimethyl-aminophenyl-methyl]-2,4,6-trihydroxyphenyl]ethanone(1224583-53-2)

Safety Data

• Hazardous Substances Data: 1224583-53-2(Hazardous Substances Data)

Upstream product

• 2161-86-6 2,4-diacetylphloroglucinol 
• 100-10-7 4-dimethylamino-benzaldehyde 

Relevant articles and documents

Biomimetic synthesis and anti-HIV activity of dimeric phloroglucinols

Plants are an important source of a variety of bioactive compounds with different modes of action. Anti-HIV agents from plant sources can be useful in developing novel therapies for inhibiting HIV infection. Based on the reported anti-HIV activity of plant derived phloroglucinols, several new dimeric phloroglucinols were synthesized in the present study by varying substitution on aromatic ring and at methylene bridge. Some of the synthesized compounds have shown good HIV inhibitory activity in a human CD4+ T cell line (CEM-GFP) infected with HIV-1 NL4.3 virus isolate. Structure-activity studies indicate that phenyl, 4-benzyloxy-1-phenyl and cyclohexyl substitution at methylene bridge gave compounds with better anti-HIV activity. Compounds 22 and 24 showed highest anti-HIV activity with an IC50 of 0.28 μM and 2.71 μM, respectively, former was more active than the positive standard AZT in cell based assay.