Boceprevir
Boceprevir is a potent and selective inhibitor of hepatitis C virus (HCV) protease NS3 with Ki value of 14 nM [1].
HCV is a type of RNA virus and infects about 300 million people worldwide. As a serine protease of HCV, NS3 plays an important role in the replication process of HCV when the virus enters the host cell. NS3 processes the polyprotein translated from the virus RNA genome and promotes the maturation of the virus. NS3 is also found to restore the interferon-sensitive signaling pathway. Due to these features, NS3 is thought to be the appropriate target for the therapy of antivirus. The SAR studies led to the discovery of boceprevir (also named as SCH 503034). Boceprevir has a ketoamide group, it binds NS3 and forms a covalent and reversible adduct with the active site serine [1, 2 and 3].
In the cell-based replicon assay using hepatocytes, boceprevir showed improved potency than other derivatives with IC90 value of 350 nM. The selectivity of boceprevir was tested by binding to human neutrophil elastase which had similar structure with NS3. Boceprevir exerted a great selectivity with a HNE/HCV ratio of 2200. It is approximately 15-fold more selective than the corresponding carbamate derivative. In MTS assay, the compound showed no significant cytotoxicity even when its concentration was up to 50 μM [1].
Boceprevir is an orally bioavailable inhibitor of HCV NS3 protease. In rats, oral administration of boceprevir showed AUC value of 1.5 μM•H and bioavailability of 26%. In dogs, boceprevir demonstrated a 30% bioavailability with AUC value of 3.1μM•H at a dose of 3 mg/kg. Boceprevir was also used as a combination therapy with the pegylated interferon (PEG-IFN-α-2B). It was found that the combination showed at least addictive potency compared with each one alone [1, 2].
References:
1.Venkatraman S, Bogen S L, Arasappan A, et al. Discovery of (1 R, 5 S)-N-[3-Amino-1-(cyclobutylmethyl)-2, 3-dioxopropyl]-3-[2 (S)-[[[(1, 1-dimethylethyl) amino] carbonyl] amino]-3, 3-dimethyl-1-oxobutyl]-6, 6-dimethyl-3-azabicyclo [3.1. 0] hexan-2 (S)-carboxamide (SCH 503034), a Selective, Potent, Orally Bioavailable Hepatitis C Virus NS3 Protease Inhibitor: A Potential Therapeutic Agent for the Treatment of Hepatitis C Infection. Journal of medicinal chemistry, 2006, 49(20): 6074-6086.
2.Sarrazin C, Rouzier R, Wagner F, et al. SCH 503034, a novel hepatitis C virus protease inhibitor, plus pegylated interferon α-2b for genotype 1 nonresponders. Gastroenterology, 2007, 132(4): 1270-1278.
3.Flores M V, Strawbridge J, Ciaramella G, et al. HCV-NS3 inhibitors: determination of their kinetic parameters and mechanism. Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics, 2009, 1794(10): 1441-1448.
Physical Appearance | A solid |
Storage | Store at -20°C |
M.Wt | 519.68 |
Cas No. | 394730-60-0 |
Formula | C27H45N5O5 |
Synonyms | Boceprevir ,EBP 520;SCH 503034;EBP-520;EBP520;SCH-503034;SCH503034 |
Solubility | ≥25.98 mg/mL in DMSO; insoluble in H2O; ≥89.8 mg/mL in EtOH |
Chemical Name | (1R,2S,5S)-N-(4-amino-1-cyclobutyl-3,4-dioxobutan-2-yl)-3-[(2S)-2-(tert-butylcarbamoylamino)-3,3-dimethylbutanoyl]-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carboxamide |
SDF | Download SDF |
Canonical SMILES | CC1(C2C1C(N(C2)C(=O)C(C(C)(C)C)NC(=O)NC(C)(C)C)C(=O)NC(CC3CCC3)C(=O)C(=O)N)C |
Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
General tips | We do not recommend long-term storage for the solution, please use it up soon. |
Cell experiment:[1] | |
Cell lines |
HuH-7 cells |
Reaction Conditions |
For 72 h incubation |
Applications |
The EC50 and EC90 values of boceprevir on HuH-7 cells bearing the subgenomic hepatitis C virus (HCV) replicon were determined to be 0.20 µM and 0.35 µM, respectively. |
Animal experiment:[2] | |
Animal models |
NS3/4A/Lap/LC-1 triple-transgenic mice induced with doxycycline |
Dosage form |
100 mg/kg Twice daily by oral gavage for 7 days |
Applications |
Oral administration of boceprevir led to a 65% reduction in the average plasma Gaussia luciferase (Gluc) activity. Notably, Gluc activity gradually reverted back to the pre-treatment level when boceprevir treatment ceased. |
Note |
The technical data provided above is for reference only. |
References: 1. Njoroge FG, Chen KX, Shih NY, et al. Challenges in modern drug discovery: a case study of boceprevir, an HCV protease inhibitor for the treatment of hepatitis C virus infection. Accounts of Chemical Research, 2008, 41(1): 50-59. 2. Yao M, Lu X, Lei Y, et al. Conditional Inducible Triple-Transgenic Mouse Model for Rapid Real-Time Detection of HCV NS3/4A Protease Activity. PLoS One, 2016, 11(3): e0150894. |
Description | Boceprevir(EBP-520, SCH503034) is an inhibitor of HCV protease with a Ki value of 14 nM. | |||||
Targets | HCV protease | |||||
IC50 | 14 nM (Ki) |
Quality Control & MSDS
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Chemical structure
