Description
Raltegravir is an antiviral compound that inhibits HIV integrase; it is clinically used to treat HIV infection. In pre-clinical models, raltegravir decreases infection rates by preventing insertion of HIV-1 DNA into the host genome.
| Product Unit Size | Cost | Quantity | Stock |
|---|
Raltegravir is an antiviral compound that inhibits HIV integrase; it is clinically used to treat HIV infection. In pre-clinical models, raltegravir decreases infection rates by preventing insertion of HIV-1 DNA into the host genome.
| Cas No. | 518048-05-0 |
|---|---|
| Purity | ≥99% |
| Formula | C20H21FN6O5 |
| Formula Wt. | 444.42 |
| IUPAC Name | N-(4-Fluorobenzyl)-5-hydroxy-1-methyl-2-(2-{[(5-methyl-1,3,4-oxadiazol-2-yl)carbonyl]amino}-2-propanyl)-6-oxo-1,6-dihydro-4-pyrimidinecarboxamide |
| Synonym | MK-0518 |
| Solubility | soluble in water, slightly soluble in methanol, very slightly soluble in ethanol and acetonitrile and insoluble in isopropanol. The solubility of raltegravir increases with increasing pH such that its solubility in water is approx. 71 mg/mL. Its pKa is 6.3 |
| Appearance | White to off white powder |
| Store Temp | -20°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet | |
| Brochures |
Taramasso L, Madeddu G, Ricci E, et al. Raltegravir-based therapy in a cohort of HIV/HCV co-infected individuals. Biomed Pharmacother. 2015 Feb;69:233-6. PMID: 25661363.
Mouscadet JF, Tchertanov L. Raltegravir: molecular basis of its mechanism of action. Eur J Med Res. 2009 Nov 24;14 Suppl 3:5-16. PMID: 19959411.
Hicks C, Gulick RM. Raltegravir: the first HIV type 1 integrase inhibitor. Clin Infect Dis. 2009 Apr 1;48(7):931-9. PMID: 19231980.
Tetrapeptide, IgG Fc region derivative; Nrp1 ag...
nNOS inhibitor.
Peptide, involved in neutrophil activation; FPR...
Pentacyclic triterpene found in the Banaba plan...
Notch inhibitor.
GPR17 agonist, NMDA and fructose 1,6-bisphospha...
Polyether cationic ionophore.
Xanthine derivative; adenosine A2 antagonist, P...
Synthetic ITC.
Enone.
Endogenous opioid peptide; μOR agonist.
CHK1 inhibitor.
Amphiphilic properties
Aminoglycoside; protein translation inhibitor.<...
Folate analog; thymidylate synthase inhibitor.<...
Cysteine conjugate of benzyl isothiocyanate (BI...
Diterpene found in brewed, unfiltered coffee; F...
Impurity of omeprazole
Non-chlorinated analogue of the mycotoxin Ochra...