 | This articleneeds attention from an expert in Pharmacology. The specific problem is:non-antiviral types inTemplate:Enzyme inhibition.WikiProject Pharmacology may be able to help recruit an expert.(January 2020) |
Protease inhibitors (PIs) aremedications that act by interfering withenzymes that cleave proteins. Some of the most well known areantiviral drugs widely used to treatHIV/AIDS,hepatitis C andCOVID-19. These protease inhibitors prevent viral replication by selectively binding to viralproteases (e.g.HIV-1 protease) and blocking proteolytic cleavage of protein precursors that are necessary for the production of infectiousviral particles.
Protease inhibitors that have been developed and are currently used in clinical practice include:
Given the specificity of the target of these drugs there is the risk, like withantibiotics, of the development of drug-resistant mutated viruses. To reduce this risk, it is common to use several different drugs together that are each aimed at different targets.
In addition to those non-human proteases listed above, inhibitors of human proteases may be used to treat cancer. See the articlesmatrix metalloproteinase inhibitor (–mastat) andproteasome inhibitor (–zomib).[1]
Antiretroviral protease inhibitors act by binding to the catalytic site of HIV protease, preventing cleavage of viral polyprotein precursor proteins into functional viral proteins required for viral replication.[4] Most ARPIs are peptide-like molecules which resemble the substrate of the viral protease.[4]
Protease inhibitors were the second class ofantiretroviral drugs developed. The first members of this class,saquinavir,ritonavir, andindinavir, were approved in late 1995–1996. Within two years, annual deaths from AIDS in the United States fell from over 50,000 to approximately 18,000.[5] Prior to this the annual death rate had been increasing by approximately 20% each year.
| Name | Trade name | Company | Patent | FDA approval date | Notes |
|---|---|---|---|---|---|
| Saquinavir | Invirase, Fortovase | Hoffmann–La Roche | U.S. patent 5,196,438 | December 6, 1995 | The first protease inhibitor approved by theU.S. Food and Drug Administration (FDA). |
| Ritonavir | Norvir | AbbVie | U.S. patent 5,541,206 | March 1, 1996 | AbbVie was part of Abbott Laboratories when patent was granted. As well as being a protease inhibitor in its own right, ritonavir inhibits the breakdown of other protease inhibitors. This property makes it very useful in drug combinations.[6] |
| Indinavir | Crixivan | Merck & Co. | U.S. patent 5,413,999 | March 13, 1996 | — |
| Nelfinavir | Viracept | Hoffmann–La Roche | U.S. patent 5,484,926 | March 14, 1997 | — |
| Amprenavir | Agenerase | GlaxoSmithKline | U.S. patent 5,585,397 | April 15, 1999 | The sixteenth FDA-approved antiretroviral. It was the first protease inhibitor approved for twice-a-day dosing instead of needing to be taken every eight hours. The convenient dosing came at a price, as the dose required is 1,200 mg, delivered in 8 very large gel capsules. Production was discontinued by the manufacturer December 31, 2004, as it has been superseded by fosamprenavir. |
| Lopinavir | Kaletra | AbbVie | U.S. patent 5,914,332 | September 15, 2000 | Is only marketed as a fixed-dose combination with ritonavir (seelopinavir/ritonavir). AbbVie was part of Abbott Laboratories when patent was granted. |
| Atazanavir | Reyataz | Bristol-Myers Squibb | U.S. patent 5,849,911 | June 20, 2003 | Atazanavir was the first PI approved for once-daily dosing. It appears to be less likely to cause lipodystrophy and elevated cholesterol as side effects. It may also not be cross-resistant with other PIs. |
| Fosamprenavir | Lexiva, Telzir | GlaxoSmithKline | — | October 20, 2003 | Aprodrug of amprenavir. The human body metabolizes fosamprenavir in order to form amprenavir, which is the active ingredient. That metabolization increases the duration that amprenavir is available, making fosamprenavir aslow release version of amprenavir and thus reduces the number of pills required versus standard amprenavir. |
| Tipranavir | Aptivus | Boehringer Ingelheim | — | June 22, 2005 | Also known as tipranavir disodium. |
| Darunavir | Prezista | Janssen Therapeutics | U.S. patent 6,248,775 | June 23, 2006 | As of 2016, darunavir is anOARAC recommended treatment option for treatment-naïve and treatment-experienced adults and adolescents.[7] Several ongoingphase III trials are showing a high efficiency for the darunavir/ritonavir combination being superior to thelopinavir/ritonavir combination for first-line therapy.[8] Darunavir is the first drug in a long time that did not come with a price increase. Itleapfrogged two other approved drugs of its type, and is matching the price of a third.[9][10][11] |
A drug combination targeting SARS-CoV-2,Paxlovid, was approved in December 2021 to treat COVID-19.[12] It is a combination ofnirmatrelvir, a protease inhibitor targeted to the SARS-CoV-23C-like protease, and ritonavir, which inhibits the metabolism of nirmatrelvir, thereby prolonging its effect.[13]
Protease inhibitors can cause a syndrome oflipodystrophy,hyperlipidemia,diabetes mellitus type 2, andkidney stones.[14] This lipodystrophy is colloquially known as "Crix belly", afterindinavir (Crixivan).[15]