Raltegravir
CAS: 518048-05-0
Ref. 3D-FR29048
| 1g | 390.00 € | ||
| 2g | 550.00 € | ||
| 5g | 1,025.00 € | ||
| 10g | 1,607.00 € | ||
| 500mg | 272.00 € |
Product Information
- N-((4-Fluorophenyl)methyl)-1,6-dihydro-5-hydroxy-1-methyl-2-(1-methyl-1-(((5-methyl-1,3,4-oxadiazol-2-yl)carbonyl)amino)ethyl)-6-oxo -4-pyrimidinecarboxamide
- 4-Pyrimidinecarboxamide, N-[(4-fluorophenyl)methyl]-1,6-dihydro-5-hydroxy-1-methyl-2-[1-methyl-1-[[(5-methyl-1,3,4-oxadiazol-2-yl)carbonyl]amino]ethyl]-6-oxo-
- 5-Hydroxy-2-[1-[[(5-Methyl-1,3,4-oxadiazol-2-yl)carbonyl]amino]-1-methylethyl]-N-(4-fluorobenzyl)-1-methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide
- N-(4-fluorobenzyl)-5-hydroxy-1-methyl-2-(1-methyl-1-{[(5-methyl-1,3,4-oxadiazol-2-yl)carbonyl]amino}ethyl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide
- N-[(4-Fluorophenyl)methyl]-1,6-dihydro-5-hydroxy-1-methyl-2-[1-methyl-1-[[(5-methyl-1,3,4-oxadiazol-2-yl)carbonyl]amino]ethyl]-6-oxo-4-pyrimidinecarboxamide
Raltegravir is an antiviral drug that is used in the treatment of HIV-1 infection. It has been shown to be highly effective in preventing viral resistance to other antiretroviral drugs, such as protease inhibitors, by inhibiting the replication of HIV-1. Raltegravir binds noncompetitively to the reverse transcriptase enzyme and prevents it from converting single-stranded RNA into double-stranded DNA. In addition, raltegravir inhibits the activity of proteases and polymerases that are necessary for viral replication. Raltegravir has been shown to inhibit the growth of resistant mutants at a concentration of 250 nanomolar. The chemical structure of this drug was determined using X-ray crystallography and nuclear magnetic resonance spectroscopy.
Chemical properties
Technical inquiry about: 3D-FR29048 Raltegravir
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