701213-28-7

Basic information

• Product Name: C₂₃H₂₀FN₇O₃
• CAS NO: 701213-28-7
• Molecular Weight: 461.455
• Mol File: 701213-28-7.mol

Chemical Properties

• CAS DataBase Reference: C₂₃H₂₀FN₇O₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₃H₂₀FN₇O₃(701213-28-7)
• EPA Substance Registry System: C₂₃H₂₀FN₇O₃(701213-28-7)

Safety Data

• Hazardous Substances Data: 701213-28-7(Hazardous Substances Data)

Upstream product

• 446284-38-4 7-bromo-4-fluoro-1H-pyrrolo[2,3-c]pyridine 
• 7170-01-6 3-methyl-1H-[1,2,4]triazole 
• 701213-94-7 1-(4-benzoylpiperazin-1-yl)-2-(7-bromo-4-fluoro-1H-pyrrolo[2,3-c]pyridin-3-yl)ethane-1,2-dione 
• 639519-63-4 2-(7-bromo-4-fluoro-1H-pyrrolo[2,3-c]pyridin-3-yl)-2-oxoacetic acid 
• 136888-20-5 5-fluoro-2-hydroxy-3-nitropyridine 
• 51173-05-8 5-fluoropyridin-2-ol 
• 51173-04-7 5-fluoro-2-methoxypyridine 
• 6628-77-9 6-methoxy-pyridin-3-ylamine 

Relevant articles and documents

Inhibitors of human immunodeficiency virus type 1 (HIV-1) attachment. 12. Structure-activity relationships associated with 4-fluoro-6-azaindole derivatives leading to the identification of 1-(4-benzoylpiperazin-1-yl)-2-(4- fluoro-7-[1,2,3]triazol-1-yl-1H-

A series of highly potent HIV-1 attachment inhibitors with 4-fluoro-6-azaindole core heterocycles that target the viral envelope protein gp120 has been prepared. Substitution in the 7-position of the azaindole core with amides (12a,b), C-linked heterocycl

Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives

This invention provides compounds having drug and bio-affecting properties, their pharmaceutical compositions and method of use. In particular, the invention is concerned with azaindoleoxoacetyl piperazine derivatives. These compounds possess unique antiviral activity, whether used alone or in combination with other antivirals, antiinfectives, immunomodulators or HIV entry inhibitors. More particularly, the present invention relates to the treatment of HIV and AIDS.