2. Anti-infection
  3. HBV
  4. 1132940-31-8

1132940-31-8

ABT-072 potassium trihydrate Chemical Structure

1132940-31-8

Chemical Structure

  • ABT-072 potassium trihydrate
  • CAS No: 1132940-31-8
    Formula: C24H32KN3O8S
    Molecular Weight: 561.69
  • IUPAC Name: potassium (E)-(4-(3-(tert-butyl)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxystyryl)phenyl)(methylsulfonyl)amide trihydrate
  • InChIKey: YOVHIDHQVIZCEH-MPMAQEBPSA-N
  • SMILES: CS(=O)([N-]C1=CC=C(/C=C/C2=CC(N(C(N3)=O)C=CC3=O)=CC(C(C)(C)C)=C2OC)C=C1)=O.[H]O[H].[H]O[H].[H]O[H].[K+]

Biological Activity: ABT-072 (potassium trihydrate) is an orally active and potent non-nucleoside HCV NS5B polymerase inhibitor (HCV GT1a EC50=1 nM; HCV GT1b EC50=0.3 nM)[1][2][3].

Cat. No. Product Name Purity Description
HY-155700 SDH-IN-6 SDH-IN-6 (compound 6i) is a potent succinate dehydrogenase (SDH) inhibitor. SDH-IN-6 has antifungal activity against Valsa mali with an EC50 value of 1.77 mg/L.

References

[1]. Lawitz E, et al. A phase 2a trial of 12-week interferon-free therapy with two direct-acting antivirals (ABT-450/r, ABT-072) and ribavirin in IL28B C/C patients with chronic hepatitis C genotype 1. J Hepatol. 2013;59(1):18-23. [Content Brief]
[2]. Shi Y, et al. Assessing Supersaturation and Its Impact on In Vivo Bioavailability of a Low-Solubility Compound ABT-072 With a Dual pH, Two-Phase Dissolution Method. J Pharm Sci. 2016;105(9):2886-2895. [Content Brief]
[3]. Randolph JT, et al. Synthesis and Biological Characterization of Aryl Uracil Inhibitors of Hepatitis C Virus NS5B Polymerase: Discovery of ABT-072, a trans-Stilbene Analog with Good Oral Bioavailability. J Med Chem. 2018;61(3):1153-1163. [Content Brief]

Keywords:

ABT-072 potassium trihydrate