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RO8191

Cat. No. M30500
RO8191 Structure
Synonym:

CDM-3008; RO4948191

Size Price Availability Quantity
5mg USD 105  USD105 In stock
10mg USD 175  USD175 In stock
25mg USD 360  USD360 In stock
50mg USD 540  USD540 In stock
100mg USD 800  USD800 In stock
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Quality Control & Documentation
Biological Activity

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. RO8191 is a cccDNA modulator (CDM) through interferon-like activity and has anti-HBV activity.

Chemical Information
Molecular Weight 373.21
Formula C14H5F6N5O
CAS Number 691868-88-9
Form Solid
Solubility (25°C) DMSO 5 mg/mL (ultrasonic and warming and heat to 60°C)
Storage -20°C, sealed
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Xiao-Ling Luo, et al. Adv Sci (Weinh). hESC-Derived Epicardial Cells Promote Repair of Infarcted Hearts in Mouse and Swine

[2] Jiguang Meng, et al. Environ Toxicol. EPN3 plays oncogenic role in non-small cell lung cancer by activating the JAK1/2-STAT3 pathway

[3] Uriel Enrique Aquino Ruiz, et al. Virus Res. Imidazonaphthyridine effects on Chikungunya virus replication: Antiviral activity by dependent and independent of interferon type 1 pathways

[4] Jiefei Zhu, et al. Immunogenetics. IL4I1 enhances PD-L1 expression through JAK/STAT signaling pathway in lung adenocarcinoma

[5] Huan Wang, et al. ACS Med Chem Lett. Discovery of Imidazo[1,2-α][1,8]naphthyridine Derivatives as Potential HCV Entry Inhibitor

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Keywords: RO8191, CDM-3008; RO4948191 supplier, Interferon-α/β/γ, inhibitors, activators


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