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Pathways

PathWhiz ID Pathway Meta Data

PW127504

Pw127504 View Pathway
drug action

Tipranavir Action Pathway

Homo sapiens
Tipranavir is a sulfonamide-containing dyhydropyrone and a nonpeptidic protease inhibitor used to treat HIV-1 resistant to more than 1 protease inhibitor. Protease inhibitors are almost always used in combination with at least two other anti-HIV drugs. The HIV virus binds and penetrates the host cell. Viral RNA is transcribed into viral DNA via reverse transcriptase. Viral DNA enters the host nucleus and is integrated into the host DNA via integrase. The DNA is then transcribed, creating viral mRNA. Viral mRNA is translater into the gag-pol polyprotein. HIV protease is synthesized as part of the Gag-pol polyprotein, where Gag encodes for the capsid and matrix protein to form the outer protein shell, and Pol encodes for the reverse transcriptase and integrase protein to synthesize and incorporate its genome into host cells. HIV-1 protease cleaves the Gag-pol polyprotein into 66 molecular species, including HIV-1 protease, integrase, and reverse transcriptase. Tipranavir competitively binds to the active site of HIV-1 protease. This inhibition prevents the HIV virion from fully maturing and becoming infective. Using the lipid bilayer of the host cell, a virus is formed and released. The inhibition of HIV-1 protease prevents the necessary molecular species from forming, therefore preventing maturation and activation of viral particles. This forms immature, non-infectious viral particles, therefore, Tipranavir prevents the virus from reproducing.

PW145032

Pw145032 View Pathway
drug action

Tipranavir Drug Metabolism Action Pathway

Homo sapiens

PW176147

Pw176147 View Pathway
metabolic

Tipranavir Predicted Metabolism Pathway new

Homo sapiens
Metabolites of Tipranavir are predicted with biotransformer.

PW145656

Pw145656 View Pathway
drug action

Tirbanibulin Drug Metabolism Action Pathway

Homo sapiens

PW122410

Pw122410 View Pathway
drug action

Tirofiban Action

Homo sapiens
Tirofiban is a platelet aggregation inhibitor drug sold under the name Aggrastat. It is specifically a small molecule that inhibits the glycoprotein IIb/IIIa receptor of platelets. It is administered intravenously, and can act to decrease platelet aggregation by over 90% after the infusion, and can help prevent aggregation for up to two days after administration. In the vein, tirofiban causes a conformational change in the integrins on the surface of activated platelets. This prevents the binding of fibrinogen to these integrins, which in turn prevents the platelets from being held together by these fibrinogen fibres. The conformational change also prevents the binding of von Willebrand factor to the platelets, which also prevents aggregation and adhesion.

PW000293

Pw000293 View Pathway
drug action

Tirofiban Action Pathway

Homo sapiens
Tirofiban is a platelet aggregation inhibitor drug sold under the name Aggrastat. It is specifically a small molecule that inhibits the glycoprotein IIb/IIIa receptor of platelets. It is administered intravenously, and can act to decrease platelet aggregation by over 90% after the infusion, and can help prevent aggregation for up to two days after administration. In the vein, tirofiban causes a conformational change in the integrins on the surface of activated platelets. This prevents the binding of fibrinogen to these integrins, which in turn prevents the platelets from being held together by these fibrinogen fibres. The conformational change also prevents the binding of von Willebrand factor to the platelets, which also prevents aggregation and adhesion.

PW128069

Pw128069 View Pathway
drug action

Tirofiban Action Pathway (new)

Homo sapiens
Tirofiban is a platelet aggregation inhibitor, also known under the brand name Aggrastat, it is used to prevent thrombotic events from occurring in those who are high-risk. It is administered intravenously and acts as an antagonist of the platelet glycoprotein IIb/IIIa receptor, this receptor is responsible for platelet aggregation in order to form a thrombus, without this signal from the receptor it stops aggregation. This inhibition created by the drug will cease once the drug is no longer infused into the patient's bloodstream.

PW144884

Pw144884 View Pathway
drug action

Tirofiban Drug Metabolism Action Pathway

Homo sapiens

PW146190

Pw146190 View Pathway
drug action

Titanium dioxide Drug Metabolism Action Pathway

Homo sapiens

PW128525

Pw128525 View Pathway
drug action

Tivozanib Action Pathway

Homo sapiens
Tivozanib, marketed as FOTIVDA, is a kinase inhibitor primarily used to treat renal cell carcinoma (RCC) in adult patients who have not responded to previous systemic therapies or have experienced relapsed disease. RCC is a relatively common cancer that predominantly affects adults between the ages of 65 to 74. Tivozanib offers hope as a therapeutic option for individuals with advanced RCC who have not had success with other treatments. It is approved in the United States for those who have undergone two or more systemic therapies for RCC. In the UK and some other countries, it is indicated as the first-line therapy for adults with advanced RCC who have not previously received VEGFR and mTOR pathway inhibitors after their disease has progressed following one prior treatment with cytokine therapy. Tivozanib works by inhibiting growth factor receptors, specifically targeting renal cell carcinoma. In preclinical studies using mice and rats, tivozanib demonstrated its ability to inhibit tumor angiogenesis, slow tumor growth, and reduce vascular permeability. However, it's important to note that tivozanib can often lead to hypertension, which must be managed before initiating therapy. Additionally, while a cardiac QT segment prolongation was reported in a tivozanib cardiac safety study, these reactions were not deemed clinically serious. Furthermore, clinical studies have shown a decrease in serum soluble VEGFR2 (sVEGFR2) levels over time with tivozanib exposure, and sVEGFR2 can serve as a pharmacodynamic marker of VEGFR inhibition.