Customization: | Available |
---|---|
Type: | Pharmaceutical Intermediates |
Appearance: | Powder |
Still deciding? Get samples of $ !
Request Sample
|
Suppliers with verified business licenses
4-[[4-[[4-[(E)-2-cyanoethenyl]-2,6-dimethyl-phenyl]amino]pyrimidin-2-yl]amino]benzo nitrile Chemical Properties |
Melting point | 245ºC |
Boiling point | 634.1±65.0 °C(Predicted) |
density | 1.27 |
storage temp. | Refrigerator |
pka | 4.56±0.10(Predicted) |
Safety Information |
Hazardous Substances Data | 500287-72-9(Hazardous Substances Data) |
MSDS Information |
4-[[4-[[4-[(E)-2-cyanoethenyl]-2,6-dimethyl-phenyl]amino]pyrimidin-2-yl]amino]ben zonitrile Usage And Synthesis |
Description | In May 2011, the U.S. FDA approved rilpivirine in combination with other antiretroviral agents for the treatment of human immunodeficiency virus (HIV) 1 infection in treatment-naive adult patients. Rilpivirine is a member of the nonnucleoside reverse transcriptase inhibitor (NNRTI) class of anti-HIV agents. It is highly potent against a range of wild-type HIV strains (EC50=0.07-1.0 nM),~10-20 timesmore potent than the NNRTI efavirenz (Sustiva), and active against HIV strains resistant to other NNRTIs. The discovery of rilpivirine was guided by molecular modeling and X-ray crystallography of HIV-1 RT complexed with inhibitors. The synthesis of rilpivirine is accomplished by an efficient 6-step route in which the key step is coupling of 4-((4-chloropyrimidin-2-yl)amino)benz onitrile with (E)-3-(4-amino-3,5-dimethylphenyl)acrylonit rile. |
Chemical Properties | N/ABright Yellow Solid |
Originator | Janssen (Belgium) |
Uses | A novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. An anti-HIV agent. |
Uses | A novel non-nucleoside reverse transcriptase inhibitor. Rilpivirine seems to be well tolerated with less CNS disturbance than Efavirenz, and has non-teratogenic potential. |
Definition | ChEBI: An aminopyrimidine that is pyrimidine-2,4-diamine in which the amino groups at positions 2 and 4 are substituted by 4-cyanophenyl and 4-[(E)-2-cyanovinyl]-2,6-dimethylphenyl groups respectively. Used for treatment of HIV. |
Brand name | Edurant |