ccc_R08
CAS No. 2919019-72-8
ccc_R08( —— )
Catalog No. M36524 CAS No. 2919019-72-8
ccc_R08 is an orally available HBV cccDNA inhibitor that reduces extracellular levels of HBV DNA, HBsAg, and HBeAg in a dose-dependent manner. ccc_R08 is investigational for use in the treatment of HBV infections. ccc_R08 has been shown to be effective in the treatment of hepatitis C virus (HCV).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 242 | Get Quote |
|
| 5MG | 337 | Get Quote |
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| 10MG | 506 | Get Quote |
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| 25MG | 1030 | Get Quote |
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| 50MG | 1371 | Get Quote |
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| 100MG | 1782 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
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Biological Information
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Product Nameccc_R08
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NoteResearch use only, not for human use.
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Brief Descriptionccc_R08 is an orally available HBV cccDNA inhibitor that reduces extracellular levels of HBV DNA, HBsAg, and HBeAg in a dose-dependent manner. ccc_R08 is investigational for use in the treatment of HBV infections. ccc_R08 has been shown to be effective in the treatment of hepatitis C virus (HCV).
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Descriptionccc_R08 is a non-cytotoxic and orally active cccDNA inhibitor that reduces cccDNA levels in the liver of HBV-infected mice. ccc_R08 can be used in the study of HBV virus (hepatitis B virus) infection.
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In Vitroccc_R08 (0.3, 1.0, 3.2, 10, 32 μM; 5 days) significantly reduces the level of cccDNA, protein-free RC-DNA, and double stranded linear DNA (DL-DNA) in HepDES19 cells.ccc_R08 (0-100 μM) dose-dependently reduces the level of extracellular HBeAg from HepDES19 cells, with IC50 of ~0.1 μM.Western Blot Analysis Cell Line:HepDES19 cells Concentration:0.3, 1.0, 3.2, 10, 32 μM Incubation Time:5 days Result:Reduced the level of cccDNA, protein-free RC-DNA, and double stranded linear DNA (DL-DNA).
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In Vivoccc_R08 (20 mg/kg; p.o.; twice per day for 2 weeks) clears cccDNA from the liver of HBVcircle mice.ccc_R08 (10, 15, 20, 30 mg/kg; p.o.; twice per day for 2 weeks) significantly decreases the serum level of pgRNA in a dose-dependent manner, and the reduction in pgRNA is quantitatively correlated with that in liver cccDNA at different doses.Animal Model:HBVcircle mouse model .Dosage:20 mg/kg Administration:Oral administration; twice per day for 2 weeks Result:Led to the clearance of cccDNA from HBVcircle mouse livers.Animal Model:HBVcircle mouse model .Dosage:10, 15, 20, 30 mg/kg Administration:Oral administration; twice per day for 42 days Result:Led to a sustained reduction in the serum levels of pgRNA.
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Synonyms——
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PathwayMicrobiology/Virology
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TargetHBV
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RecptorHBV
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Research Area——
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Indication——
Chemical Information
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CAS Number2919019-72-8
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Formula Weight414.84
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Molecular FormulaC22H19ClO6
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (241.06 mM; Ultrasonic )
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SMILESO=C(O)C1CC(OCCOC=2C=CC(=CC2)C=3OC=4C(Cl)=CC=CC4C(=O)C3)C1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Wang L, et al. Discovery of a first-in-class orally available HBV cccDNA inhibitor. J Hepatol. 2022 Dec 29:S0168-8278(22)03466-3. ?
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