Rilpivirine
- Rilpivirine
-
Rilpivirine |
|
Général |
Nom IUPAC |
4-{[4-({4-[(E)-2-cyanoéthényl]-2,6-diméthylphényl}amino)pyrimidin-2-yl]amino}benzonitrile |
No CAS |
500287-72-9 |
SMILES |
|
InChI |
InChI : Vue 3D
InChI=1/C22H18N6/c1-15-12-18(4-3-10-23)13-16(2)21(15)27-20-9-11-25-22(28-20)26-19-7-5-17(14-24)6-8-19/h3-9,11-13H,1-2H3,(H2,25,26,27,28)/b4-3+
|
Propriétés chimiques |
Formule brute |
C22H18N6 [Isomères]
|
Masse molaire[1] |
366,4185 ± 0,0201 g·mol-1
C 72,11 %, H 4,95 %, N 22,94 %,
|
Unités du SI & CNTP, sauf indication contraire.
|
La rilpivirine (TMC 278) est un médicament antirétroviral à l'étude (mai 2008), c'est un analogue non-nucléosidiques, inhibiteurs de la transcriptase inverse (nNRTI) actuellement développé pour le traitement de l'infection par le VIH.
Ce médicament non encore disponible est attendu en autorisation temporaire d'utilisation (ATU) à défaut éventuellement d'une autorisation de mise sur le marché (AMM) en France.
Efficacité
Elle est comparable à celle de l'éfavirenz et serait mieux tolérée que cette dernière[2],[3].
Voir aussi
Notes et références
- ↑ Masse molaire calculée d’après Atomic weights of the elements 2007 sur www.chem.qmul.ac.uk.
- ↑ Molina J-M, Cahn P, Grinsztejn B, et al, on behalf of the ECHO study group. Rilpivirine versus efavirenz with tenofovir and emtricitabine in treatment-naive adults infected with HIV-1 (ECHO): a phase 3 randomised double-blind active-controlled trial, Lancet, 2011;378:238-246
- ↑ Cohen CJ, Andrade-Villanueva J, Clotet B, et al. on behalf of the THRIVE study group. Rilpivirine versus efavirenz with two background nucleoside or nucleotide reverse transcriptase inhibitors in treatment-naive adults infected with HIV-1 (THRIVE): a phase 3, randomised, non-inferiority trial, Lancet, 2011;378:229-237
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