RO8191
CAS No. 691868-88-9
RO8191( CDM-3008 | RO4948191 )
Catalog No. M27515 CAS No. 691868-88-9
RO8191 (CDM-3008), an imidazonaphthyridine compound, is an agonist of interferon (IFN) receptor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 48 | Get Quote |
|
| 5MG | 80 | Get Quote |
|
| 10MG | 132 | Get Quote |
|
| 25MG | 290 | Get Quote |
|
| 50MG | 462 | Get Quote |
|
| 100MG | 672 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameRO8191
-
NoteResearch use only, not for human use.
-
Brief DescriptionRO8191 (CDM-3008), an imidazonaphthyridine compound, is an agonist of interferon (IFN) receptor.
-
DescriptionRO8191 (CDM-3008), an imidazonaphthyridine compound, is an agonist of interferon (IFN) receptor.(In Vitro):RO8191 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.(In Vivo):RO8191 significantly induces antiviral genes Oas1b, Mx1, and Pkr in the livers of six-week-old C57BL/6J mice.
-
In Vitro——
-
In Vivo——
-
SynonymsCDM-3008 | RO4948191
-
PathwayMicrobiology/Virology
-
TargetHCV
-
Recptorthyrotropin receptor (TSHR)
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number691868-88-9
-
Formula Weight373.218
-
Molecular FormulaC14H5F6N5O
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 5 mg/mL (13.40 mM)
-
SMILESFC(F)(F)c1cc(c2ccc3nc(cn3c2n1)-c1nnco1)C(F)(F)F
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Neumann S, et al. A new small-molecule antagonist inhibits Graves' disease antibody activation of the TSH receptor. J Clin Endocrinol Metab. 2011 Feb;96(2):548-54.
molnova catalog
related products
-
KIN101
KIN101, an isoflavone agonist of IRF-3 dependent signaling, induces IRF-3 nuclear translocation. KIN101 has antiviral activity against RNA viruses, HCV, and RSV.
-
Chlorcyclizine
CHLORCYCLIZINE is a histamine H1 antagonist and a potent hepatitis C virus (HCV) entry inhibitor.
-
4-Phenoxybenzylamine
4-Phenoxybenzylamine inhibits the function of the NS3 protein by stabilizing an inactive conformation with an IC50 of about 500 μM against HCV NS3/4a .
Cart
sales@molnova.com