BEI VERSCHLUCKEN: Bei Unwohlsein GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P305+P351+P338
BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach M?glichkeit entfernen. Weiter spülen.
P330
Mund ausspülen.
P391
Verschüttete Mengen aufnehmen.
P501
Inhalt/Beh?lter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.
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)benzonitrile with (E)-3-(4-amino-3,5-dimethylphenyl)acrylonitrile.
Chemische Eigenschaften
N/ABright Yellow Solid
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.
4-[[4-[[4-[(E)-2-cyanoethenyl]-2,6-dimethyl-phenyl]amino]pyrimidin-2-yl]amino]benzonitrile Upstream-Materialien And Downstream Produkte
RilpivirineQ: What is
Rilpivirine Q: What is the CAS Number of
Rilpivirine Q: What is the storage condition of
Rilpivirine Q: What are the applications of
Rilpivirine