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Samatasvir

Chemical Structure : Samatasvir

CAS No.: 1312547-19-5

Samatasvir (IDX-719, MK-1894, IDX719, MK1894)

Catalog No.: PC-61524Not For Human Use, Lab Use Only.

Samatasvir (IDX719) is a highly potent, selective inhibitor of HCV NS5A that effectively inhibits HCV genotype 1-5 replicons with EC50 of 2-24 pM.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Samatasvir (IDX719) is a highly potent, selective inhibitor of HCV NS5A that effectively inhibits HCV genotype 1-5 replicons with EC50 of 2-24 pM.
Samatasvir also retains full activity in the presence of HIV and hepatitis B virus (HBV) antivirals.
Samatasvir demonstrates an overall additive effect when combined with IFN-α, ribavirin, representative HCV protease, and nonnucleoside polymerase inhibitors or the nucleotide prodrug IDX184.

Physicochemical Properties

M.Wt 885.062
Formula C47H48N8O6S2
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

Methyl N-[(1R)-2-[(2S)-2-[5-[4-[6-[2-[(2S)-1-[(2S)-2-(methoxycarbonylamino)-3-methylbutanoyl]pyrrolidin-2-yl]-3H-benzimidazol-5-yl]thieno[3,2-b]thiophen-3-yl]phenyl]-1H-imidazol-2-yl]pyrrolidin-1-yl]-2-oxo-1-phenylethyl]carbamate

References

1. Bilello JP, et al. Antimicrob Agents Chemother. 2014 Aug;58(8):4431-42.

2. Vince B, et al. J Hepatol. 2014 May;60(5):920-7.

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