Bictegravir

Bictegravir
  • CAS No.:1611493-60-7
  • Grade:≥98%
  • Formula:C21H18F3N3O5
  • M.W.:449.39
  • Solvent:Soluble in DMSO.

Overview

Bictegravir is a novel, potent inhibitor of HIV-1 integrase with an IC50 of 7.5 nM for strand transfer activity. Bictegravir is a drug of the integrase inhibitor class that was copied from Dolutegravir by scientists at Gilead Sciences. Bictegravir also inhibits HIV-1 viral infection in MT-2 and MT-4 cells, CD4+ T cells, and macrophages (EC50s = 1.5, 2.5, 1.5, and 6.6 nM, respectively) without exhibiting cytotoxicity (CC50s = 10.3, 3.7, 13, and 29.8 μM, respectively). In 2016, bictegravir was in a Phase 3 trial as part of a single tablet regimen in combination with tenofovir alafenamide (TAF) and emtricitabine (FTC) for the treatment of HIV-1 infection.

Application

Products > Drug Discovery > Inhibitor | Products > Drug Discovery > Inhibitor | Infection | HIV Integrase

Product Information

  • Catalog No.: B2693-058383
  • CAS No.: 1611493-60-7
  • Molecular Formula: C21H18F3N3O5
  • Molecular Weight: 449.39
  • Purity: ≥98%
  • Storage: 2-8°C
  • Solubility: Soluble in DMSO.

Source

Original product source


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