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Ledipasvir acetone

CAS No. 1441674-54-9

Ledipasvir acetone( Ledipasvir acetone | )

Catalog No. M17299 CAS No. 1441674-54-9

Ledipasvir (GS5885) is an HCV NS5A polymerase inhibitor, used for the treatment of hepatitis C virus infection.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 65 In Stock
10MG 81 In Stock
25MG 142 In Stock
50MG 243 In Stock
100MG 421 In Stock
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Biological Information

  • Product Name
    Ledipasvir acetone
  • Note
    Research use only, not for human use.
  • Brief Description
    Ledipasvir (GS5885) is an HCV NS5A polymerase inhibitor, used for the treatment of hepatitis C virus infection.
  • Description
    Ledipasvir acetone is a hepatitis C virus (HCV) NS5A inhibitor.(In Vitro):Ledipasvir acetone is considered the active ingredient, which is converted to Ledipasvir spray-dried dispersion, an amorphous free base.
  • In Vitro
    Ledipasvir acetone is considered the active ingredient, which is converted to Ledipasvir spray-dried dispersion, an amorphous free base.
  • In Vivo
    ——
  • Synonyms
    Ledipasvir acetone |
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    HCV
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    1441674-54-9
  • Formula Weight
    947.08
  • Molecular Formula
    C52H60F2N8O7
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 39 mg/mL. 41.18 mM
  • SMILES
    CC(C)[C@@H](C(=O)N1CC2(CC2)C[C@H]1c1ncc([nH]1)c1cc2c(cc1)c1c(C2(F)F)cc(cc1)c1cc2c(cc1)nc([nH]2)[C@@H]1[C@H]2CC[C@H](C2)N1C(=O)[C@H](C(C)C)NC(=O)OC)NC(=O)OC.CC(=O)C
  • Chemical Name
    methyl ((S)-1-((S)-6-(5-(9,9-difluoro-7-(2-((1R,3S,4S)-2-((methoxycarbonyl)-L-valyl)-2-azabicyclo[2.2.1]heptan-3-yl)-1H-benzo[d]imidazol-6-yl)-9H-fluoren-2-yl)-1H-imidazol-2-yl)-5-azaspiro[2.4]heptan-5-yl)-3-methyl-1-oxobutan-2-yl)carbamate compound with propan-2-one (1:1)

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Smith MA, et al. Ann Pharmacother. 2015 Mar;49(3):343-50.
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