Bevirimat

Bevirimat
  • CAS No.:174022-42-5
  • Grade:>98%
  • Formula:C36H56O6
  • M.W.:584.83
  • Solvent:In Vitro : DMSO : ≥ 50 mg/mL(85.49 mM) In Vivo: 1.Add each solvent one by one:10% DMSO >> 40%PEG300 >> 5%Tween-80 >> 45% saline Solubility: ≥ 2.5 mg/mL (4.27 mM); Clear solution 2.Add each solvent one by one:10% DMSO >> 90% (20%SBE-β-CDin saline) Solubili

Overview

Bevirimat, also known as MPC-4326 and PA-457, is an anti-HIV drug derived from a betulinic acid-like compound, first isolated from Syzygium claviflorum, a Chinese herb. It is believed to inhibit HIV by a novel mechanism, so-called maturation inhibition. Like protease inhibitors, bevirimat and other maturation inhibitors interfere with protease processing of newly translated HIV polyprotein precursor, called gag. Bevirimat prevents this viral replication by specifically inhibiting cleavage of the capsid protein (CA) from the SP1 spacer protein.

Application

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

Product Information

  • Catalog No.: B0084-244897
  • CAS No.: 174022-42-5
  • Molecular Formula: C36H56O6
  • Molecular Weight: 584.83
  • Purity: >98%
  • Storage: Powder : -20°C 3 years 4°C 2 years In solvent: -80°C 6 months -20°C 1 months
  • Solubility: In Vitro : DMSO : ≥ 50 mg/mL(85.49 mM) In Vivo: 1.Add each solvent one by one:10% DMSO >> 40%PEG300 >> 5%Tween-80 >> 45% saline Solubility: ≥ 2.5 mg/mL (4.27 mM); Clear solution 2.Add each solvent one by one:10% DMSO >> 90% (20%SBE-β-CDin saline) Solubility: 2.5 mg/mL (4.27 mM); Suspended solution; Need ultrasonic and warming 3.Add each solvent one by one:10% DMSO >> 90%corn oil Solubility: ≥ 2.5 mg/mL (4.27 mM); Clear solution

Source

Original product source


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