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Ledipasvir (hydrochloride)

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804-HY-15602C
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  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Ledipasvir (hydrochloride) - image 1

Ledipasvir (hydrochloride)

  • CAS Number: 2128695-48-5
  • UNSPSC Description: Ledipasvir (GS-5885) hydrochloride is an inhibitor of the hepatitis C virus NS5A, with EC50s of 34 pM and 4 pM against genotype 1a and 1b replicon, respectively. Ledipasvir hydrochloride is also a SARS-CoV 3CLpro inhibitor with an IC50 of 1.62 μM[3].
  • Target Antigen: HCV; SARS-CoV
  • Type: Reference compound
  • Related Pathways: Anti-infection
  • Applications: COVID-19-anti-virus
  • Field of Research: Infection
  • Assay Protocol: https://www.medchemexpress.com/ledipasvir-hydrochloride.html
  • Solubility: 10 mM in DMSO
  • Smiles: O=C(OC)N[C@H](C(N([C@H](C1=NC=C(C2=CC(C(F)(F)C3=C4C=CC(C5=CC=C6N=C([C@H]7N(C([C@@H](NC(OC)=O)C(C)C)=O)[C@]8([H])CC[C@@]7([H])C8)NC6=C5)=C3)=C4C=C2)N1)C9)CC%109CC%10)=O)C(C)C.Cl
  • Molecular Weight: 925.46
  • References & Citations: [1]Hernandez D, et al. Natural prevalence of NS5A polymorphisms in subjects infected with hepatitis C virus genotype 3 and their effects on the antiviral activity of NS5A inhibitors. J Clin Virol. 2013 May;57(1):13-8.|[2]Qi Sun, et al. Bardoxolone and bardoxolone methyl, two Nrf2 activators in clinical trials, inhibit SARS-CoV-2 replication and its 3C-like protease. Signal Transduct Target Ther. 2021 May 29;6(1):212.|[3]Link JO, et al. Discovery of ledipasvir (GS-5885): a potent, once-daily oral NS5A inhibitor for the treatment of hepatitis C virus infection. J Med Chem. 2014 Mar 13;57(5):2033-46
  • Shipping Conditions: Room temperature
  • Clinical Information: Launched