RO8191


CAS No. : 691868-88-9

(Synonyms: CDM-3008; RO4948191)

691868-88-9
Price and Availability of CAS No. : 691868-88-9
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5mg $110 In-stock
10mg $180 In-stock
25mg $342 In-stock
50mg $513 In-stock
100mg $770 In-stock
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Cat. No. : HY-W063968
M.Wt: 373.21
Formula: C14H5F6N5O
Purity: >98 %
Solubility: DMSO : 5 mg/mL (ultrasonic;warming;heat to 60°C)
Introduction of 691868-88-9 :

RO8191 (CDM-3008), an imidazonaphthyridine compound, is an orally active and potent interferon (IFN) receptor agonist. RO8191 directly binds to IFNα/β receptor 2 (IFNAR2) and activates IFN-stimulated genes (ISGs) expression and JAK/STAT phosphorylation. RO8191 shows antiviral activity against both HCV and EMCV with an IC50 of 200 nM for HCV replicon[1]. RO8191 is a cccDNA modulator (CDM) through interferon-like activity and has anti-HBV activity[2]. In Vitro: RO8191 (CDM-3008) exerts antiviral activity dependent on IFNAR2/JAK1, but is independent of IFNAR1/Tyk2. RO8191, an IFNAR2 agonist, stimulates IFN signals in mice[1].
RO8191 (0.08, 0.4, 2, 10 μM; for 72 h) strongly suppresses HCV replicon activity at 72 h in a dose-dependent manner. RO8191 reduces levels of the proteins HCV NS3 and NS4A, which are localized mainly in the perinuclear region of the replicon cells[1].
RO8191 (0.08-10 μM; for 72 h) results in the disappearance of viral proteins such as NS3, NS4A/B, and NS5A/B[1].
In Vivo: RO8191 (CDM-3008; 30 mg/kg; oral) significantly induces antiviral genes Oas1b, Mx1, and Pkr in the livers of six-week-old C57BL/6J mice[1].

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