PathWhiz ID | Pathway | Meta Data |
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PW132360View Pathway |
Tinidazole Drug MetabolismHomo sapiens
Tinidazole is a drug that is not metabolized by the human body as determined by current research and biotransformer analysis. Tinidazole passes through the liver and is then excreted from the body mainly through the kidney.
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Creator: Ray Kruger Created On: September 21, 2023 at 21:11 Last Updated: September 21, 2023 at 21:11 |
PW145012View Pathway |
drug action
Tinidazole Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 14:55 Last Updated: October 07, 2023 at 14:55 |
PW127758View Pathway |
drug action
Tinzaparin Action PathwayHomo sapiens
Tinzaparin is a low molecular weight heparin (LMWH), it is an anticoagulant that halts the formation of thrombi. It binds to antithrombin III forming a complex that speeds up the inhibition of factor Xa. This stops the generation of thrombin and the coagulation cascade, it is administered via subcutaneous injection. Through the liver, it is metabolized through sulfation and polymerization and is eliminated through the kidneys. There is some risk of osteoporosis with increasing duration of use, bleeding, alopecia, and heparin-induced thrombocytopenia (HIT). It can interact with herbs and supplements, so avoid those with anticoagulants and antiplatelet activity such as garlic, ginger, bilberry, danshen, piracetam and ginkgo bilba.
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Creator: Selena Created On: May 30, 2023 at 14:28 Last Updated: May 30, 2023 at 14:28 |
PW145822View Pathway |
drug action
Tinzaparin Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 16:45 Last Updated: October 07, 2023 at 16:45 |
PW126993View Pathway |
drug action
Tioconazole Action PathwayHomo sapiens
Tioconazole is an imidazole antifungal drug used primarily for vulvovaginal candidiasis (vaginal yeast infection), but it can be used for skin infections such as ringworm, jock itch, athlete's foot, and tinea versicolor or "sun fungus". Tioconazole is applied topically to the infected area then absorbed into the infected cell to target the fungal cells. It can also be taken orally. Terconazole inhibits lanosterol 14-alpha demethylase in the endoplasmic reticulum of fungal cells. Lanosterol 14-alpha demethylase is the enzyme that catalyzes the synthesis of 4,4'-dimethyl cholesta-8,14,24-triene-3-beta-ol from lanosterol. With this enzyme inhibited ergosterol synthesis cannot occur which causes a significant low concentration of ergosterol in the fungal cell. Ergosterol is essential in maintaining membrane integrity in fungi. Without ergosterol, the fungus cell cannot synthesize membranes thereby increasing fluidity and preventing growth of new cells. This leads to cell lysis which causes it to collapse and die.
Through unknown mechanisms, tioconazole may also inhibit endogenous respiration, interact with membrane phospholipids, inhibit the transformation of yeasts to mycelial forms and the uptake of purine, impair triglyceride and/or phospholipid biosynthesis, and inhibit the movement of calcium and potassium ions across the cell membrane by blocking the ion transport pathway known as the Gardos channel.
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Creator: Ray Kruger Created On: June 09, 2022 at 11:53 Last Updated: June 09, 2022 at 11:53 |
PW145105View Pathway |
drug action
Tioconazole Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 15:05 Last Updated: October 07, 2023 at 15:05 |
PW176237View Pathway |
Tioconazole Predicted Metabolism PathwayHomo sapiens
Metabolites of Tioconazole are predicted with biotransformer.
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Creator: Omolola Created On: December 04, 2023 at 13:05 Last Updated: December 04, 2023 at 13:05 |
PW128259View Pathway |
drug action
Tioguanine Action PathwayHomo sapiens
Tioguanine is an antineoplastic agent from the purine analog class. This drug also has antimetabolite action. Tioguanine is indicated for remission induction and remission consolidation in the treatment of acute nonlymphocytic leukemias. When this drug enters the cells, it competes with hypoxanthine and guanine for the hypoxanthine-guanine phosphoribosyltransferase (HGPRTase) and is itself converted to 6-thioguanilyic acid (TGMP), which reaches high intracellular concentrations at therapeutic doses. TGMP is a cytotoxic agent, it will interfere with the synthesis of guanine nucleotides by inhibiting the glutamine-5-phosphoribosylpyrophosphate aminotransferase (de novo pathway of purine ribonucleotide synthesis) enzyme by pseudofeedback. Furthermore, TGMP also inhibits the conversion of inosinic acid (IMP) to xanthylic acid (XMP) by competition for the enzyme IMP dehydrogenase. Thioguanine nucleotides are incorporated into both the DNA and the RNA. The final result is the sequential blockade of the usage and synthesis of purines, leading to apoptosis in the S phase of the cell cycle. This drug is administered as an oral tablet. An overdose of tioguanine may result in symptoms like nausea, vomiting, malaise, hypotension, and diaphoresis.
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Creator: Daphnee Created On: August 10, 2023 at 13:15 Last Updated: August 10, 2023 at 13:15 |
PW145823View Pathway |
drug action
Tiopronin Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 16:45 Last Updated: October 07, 2023 at 16:45 |
PW145418View Pathway |
drug action
Tiotropium Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 15:47 Last Updated: October 07, 2023 at 15:47 |