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Tipranavir

Catalog No. T4578   CAS 174484-41-4
Synonyms: PNU-140690

Tipranavir is a protease inhibitor that inhibits HIV-1 resistant to more than 1 protease inhibitor .Tipranavir effectively inhibits HIV-1 protease enzyme activity and dimerisation and has potent activity against multiple protease inhibitor (PI) HIV-1 isolates (IC50 of 66-410 nM). Tipranavir inhibits SARS-CoV-2 3CLpro activity.

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Tipranavir Chemical Structure
Tipranavir, CAS 174484-41-4
Pack Size Availability Price/USD Quantity
1 mg In stock $ 125.00
5 mg In stock $ 397.00
10 mg In stock $ 597.00
25 mg In stock $ 935.00
50 mg In stock $ 1,260.00
100 mg In stock $ 1,690.00
1 mL * 10 mM (in DMSO) In stock $ 527.00
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Purity: 99.66%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Tipranavir is a protease inhibitor that inhibits HIV-1 resistant to more than 1 protease inhibitor .Tipranavir effectively inhibits HIV-1 protease enzyme activity and dimerisation and has potent activity against multiple protease inhibitor (PI) HIV-1 isolates (IC50 of 66-410 nM). Tipranavir inhibits SARS-CoV-2 3CLpro activity.
Targets&IC50 HIV-1 (isolates):66-410 nM, HIV-1 (isolates):8 pM(Ki )
In vitro Tipranavir (PNU-140690) inhibits the enzymatic activity of HIV-1 protease, blocks the dimerization of protease subunits, and exerts potent activity against a wide spectrum of wild-type and multi-PI-resistant HIV-1 variants.[1]
In vivo Tipranavir (5 mg/kg ; mouse model): CLtot was 0.17 ± 0.10 L/h/kg, Vss was 0.51 ± 0.14 L/kg, and t1/2 was 5.4 ±0. 3h.[4]
Tipranavir (10 mg/kg ; oral ; rats): got the result of F was 30% compared to 5 mg/kg tipranavir dosing.[4]
Synonyms PNU-140690
Molecular Weight 602.66
Formula C31H33F3N2O5S
CAS No. 174484-41-4

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

Ethanol: 45.0 mg/mL (74.7 mM)

DMSO: 180.0 mg/mL (298.7 mM ), Sonication is recommended.

TargetMolReferences and Literature

1. Aoki M, et al. Loss of the protease dimerization inhibition activity of tipranavir (TPV) and its association with the acquisition of resistance to TPV by HIV-J Virol. 2012 ; 86(24):13384-13396. 2. Li F, et al. Metabolism-mediated drug interactions associated with ritonavir-boosted tipranavir in mice. Drug Metab Dispos. 2010 ; 38(5):871-878. 3. Sun Q, 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 ; 6(1):212. 4. Turner SR, et al. Tipranavir (PNU-140690): a potent, orally bioavailable nonpeptidic HIV protease inhibitor of the 5,6-dihydro-4-hydroxy-2-pyrone sulfonamide class. J Med Chem. 1998 ; 41(18):3467-3476.

Related compound libraries

This product is contained In the following compound libraries:
Drug Repurposing Compound Library EMA Approved Drug Library Inhibitor Library Anti-Viral Compound Library Clinical Compound Library FDA-Approved Drug Library Approved Drug Library Bioactive Compounds Library Max FDA-Approved & Pharmacopeia Drug Library Bioactive Compound Library

Related Products

Related compounds with same targets
Imatinib Molnupiravir PLpro inhibitor SARS-CoV-2-IN-50 SARS-CoV-2 3CLpro-IN-14 Carmofur Propiolactone SARS-CoV-2-IN-46

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Keywords

Tipranavir 174484-41-4 Microbiology/Virology Proteases/Proteasome HIV Protease SARS-CoV PNU 140690 PNU140690 PNU-140690 inhibitor inhibit

 

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