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Pibrentasvir (ABT-530) HCV Protease inhibitor

Cat.No.S9641

Pibrentasvir (ABT-530) is a novel and pan-genotypic hepatitis C virus (HCV) NS5A inhibitor, with this compound exhibiting EC50 values ranging from 1.4 pM to 5.0 pM against HCV replicons containing NS5A from genotypes 1 to 6.
Pibrentasvir (ABT-530) HCV Protease inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 1113.18

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Quality Control

Batch: S964101 DMSO]100 mg/mL]false]Ethanol]100 mg/mL]false]Water]Insoluble]false Purity: 98.35%
98.35

Solubility

In vitro
Batch:

DMSO : 100 mg/mL (89.83 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 100 mg/mL

Water : Insoluble

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Mass Concentration Volume Molecular Weight
Dilution Calculator Molecular Weight Calculator

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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%
% Tween 80
% ddH2O
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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Chemical Information, Storage & Stability

Molecular Weight 1113.18 Formula

C57H65F5N10O8

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 1353900-92-1 -- Storage of Stock Solutions

Synonyms N/A Smiles CC(C(C(=O)N1CCCC1C2=NC3=C(N2)C=C(C(=C3)F)C4CCC(N4C5=CC(=C(C(=C5)F)N6CCC(CC6)C7=CC=C(C=C7)F)F)C8=CC9=C(C=C8F)N=C(N9)C1CCCN1C(=O)C(C(C)OC)NC(=O)OC)NC(=O)OC)OC

Mechanism of Action

Targets/IC50/Ki
GT5a
(Cell-free assay)
1.4 pM(EC50)
GT1a H77
(Cell-free assay)
1.8 pM(EC50)
GT2b
(Cell-free assay)
1.9 pM(EC50)
GT4a
(Cell-free assay)
1.9 pM(EC50)
GT3a
(Cell-free assay)
2.1 pM(EC50)
GT2ab
(Cell-free assay)
2.3 pM(EC50)
GT6a
(Cell-free assay)
2.8 pM(EC50)
GT1b Con1
(Cell-free assay)
4.3 pM(EC50)
GT2a JFH-1
(Cell-free assay)
5.0 pM(EC50)
In vitro

Pibrentasvir (ABT-530) is a next-generation HCV NS5A inhibitor with potent and pan-genotypic activity, and it maintains activity against common amino acid substitutions of HCV genotypes 1 to 6 that are known to confer resistance to currently approved NS5A inhibitors.

References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT04577482 Completed
Hepatitis C Virus (HCV)
AbbVie
October 7 2020 --
NCT03303599 Completed
Hepatitis C
AbbVie
November 13 2017 --
NCT02441283 Completed
Hepatitis C
AbbVie
June 22 2015 Phase 2|Phase 3
NCT02442258 Completed
Renal Impairment
AbbVie
March 2015 Phase 1
NCT02296905 Completed
Hepatic Impairment
AbbVie
October 2014 Phase 1

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