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Ombitasvir

🥰Excellent
Catalog No. T7158Cas No. 1258226-87-7
Alias ABT-267

Ombitasvir (ABT-267) is an orally bioavailable and potent inhibitor of the hepatitis C virus (HCV) non-structural protein 5A (NS5A).with EC50s of 0.82 to 19.3 pM against HCV genotypes 1 to 5, and 366 pM against genotype 6a

Ombitasvir

Ombitasvir

🥰Excellent
Purity: 99.56%
Catalog No. T7158Alias ABT-267Cas No. 1258226-87-7
Ombitasvir (ABT-267) is an orally bioavailable and potent inhibitor of the hepatitis C virus (HCV) non-structural protein 5A (NS5A).with EC50s of 0.82 to 19.3 pM against HCV genotypes 1 to 5, and 366 pM against genotype 6a
Pack SizePriceAvailabilityQuantity
2 mg$36In Stock
5 mg$73In Stock
10 mg$113In Stock
25 mg$239In Stock
50 mg$347In Stock
100 mg$513In Stock
500 mg$1,080In Stock
1 mL x 10 mM (in DMSO)$113In Stock
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Purity:99.56%
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Product Introduction

Bioactivity
Description
Ombitasvir (ABT-267) is an orally bioavailable and potent inhibitor of the hepatitis C virus (HCV) non-structural protein 5A (NS5A).with EC50s of 0.82 to 19.3 pM against HCV genotypes 1 to 5, and 366 pM against genotype 6a
Targets&IC50
HCVs 1-5:0.82 pM-19.3 pM(EC50) , HCV 6a:366 pM(EC50)
In vivo
Ombitasvir was evaluated in vivo in a 3-day monotherapy study in 12 HCV genotype 1-infected patients at 5, 25, 50, or 200 mg dosed once daily. All patients were HCV genotype 1a infected and were without preexisting resistant variants at baseline as determined by clonal sequencing. Decreases in HCV RNA up to 3.1 log10 IU/ml were observed. Resistance-associated variants at position 28, 30, or 93 in NS5A were detected in patient samples 48 hours after the first dose. Clonal sequencing analysis indicated that wild-type virus was largely suppressed by ombitasvir during 3-day monotherapy, and at doses higher than 5 mg, resistant variant M28V was also suppressed. Ombitasvir was well tolerated at all doses, and there were no serious or severe adverse events. These data support clinical development of ombitasvir in combination with inhibitors targeting HCV NS3/4A protease (ABT-450 with ritonavir) and HCV NS5B polymerase (ABT-333, dasabuvir) for the treatment of chronic HCV genotype 1 infection[1].
Animal Research
The patients in the ombitasvir dose groups were enrolled sequentially, and within each group, patients were randomized (2:1) to either ombitasvir or placebo and treated under nonfasting conditions for 3 days while confined to the study site. The 200-mg dose group received a different formulation with higher bioavailability. Patients who received at least one dose of ombitasvir or placebo were provided the option to receive treatment with pegIFN/RBV for approximately 48 weeks once treatment with ombitasvir was completed. HCV RNA was measured using the Roche COBAS TaqMan HCV Test v2.0 real-time reverse transcriptase PCR assay (with a lower limit of quantification of 25 IU/ml and a lower limit of detection of 10 IU/ml). The virologic response was assessed as HCV RNA decrease from baseline in log10 IU/ml[1].
AliasABT-267
Chemical Properties
Molecular Weight894.11
FormulaC50H67N7O8
Cas No.1258226-87-7
SmilesCOC(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@]1(C(N)=O)c1ccc(cc1)[C@@H]1CC[C@H](N1c1ccc(cc1)C(C)(C)C)c1ccc(cc1)[C@]1(CCCN1C(=O)[C@@H](NC(=O)OC)C(C)C)C(N)=O
Relative Density.1.223 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 50 mg/mL (55.92 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.1184 mL5.5922 mL11.1843 mL55.9215 mL
5 mM0.2237 mL1.1184 mL2.2369 mL11.1843 mL
10 mM0.1118 mL0.5592 mL1.1184 mL5.5922 mL
20 mM0.0559 mL0.2796 mL0.5592 mL2.7961 mL
50 mM0.0224 mL0.1118 mL0.2237 mL1.1184 mL

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