PathWhiz ID | Pathway | Meta Data |
---|---|---|
PW175940View Pathway |
Ticlopidine Predicted Metabolism PathwayHomo sapiens
Ticlopidine PIS1M1, Ticlopidine PIS1M2, Ticlopidine PIS1M3,Ticlopidine PIS1M4, Ticlopidine PIS2M1, Ticlopidine PIS2M2, Ticlopidine PIS2M3 are metabolites of Ticlopidine predicted with biotransformer.
|
Creator: Omolola Created On: November 16, 2023 at 14:11 Last Updated: November 16, 2023 at 14:11 |
PW000689View Pathway |
drug action
Tigecycline Action PathwayHomo sapiens
Tigecycline is a glycylcycline, a class of antibiotics derived from tetracycline. Tigecycline has broad spectrum antibacterial abilities and is not susceptible to traditional tetracycline resistance mechanisms such as ribosomal protection and efflux by tetracycline-specific pumps. Tigecycline inhibits bacterial protein synthesis by binding to the A site of the 16s rRNA on the 30S ribosomal subunit. By binding to the A site, tigecycline prevents tRNA from docking onto the 16S rRNA with it’s codon ultimately halting the addition of amino acids to elongate peptide chains used in protein structures.
|
Creator: WishartLab Created On: April 26, 2014 at 16:35 Last Updated: April 26, 2014 at 16:35 |
PW124612View Pathway |
drug action
Tigecycline Anti-bacterial Action PathwayHomo sapiens
Tigecycline is an intravenous antibiotic drug used to treat infections caused by a variety of gram-positive and gram-negative microorganisms including Mycoplasma pneumoniae, Pasteurella pestis, Escherichia coli, Haemophilus influenzae (respiratory infections), and Diplococcus pneumoniae. Tigecycline first clinically-available drug in the class of glycylcyclines antibiotics. Glycylcyclines are derived from tetracycline which are analogues are specifically designed to overcome tetracycline resistance mediated by acquired efflux pumps and/or ribosomal protection. In bacterial protein synthesis, transcription and translation occur in the cytoplasm. Tigecycline targets protein translation. Translation occurs using the bacterial 70S ribosome composed of a 50S and a 30S subunit. The ribosome has 3 binding sites, A (acceptor site), P (peptidyl site) and E (exit site). The charged tRNA with an amino acid attached (amino-acyl tRNA) binds to the A site. The P site binds to the tRNA holding the growing polypeptide chain and the E site binds to the uncharged tRNA.
|
Creator: Kristen Yee Created On: March 29, 2021 at 22:17 Last Updated: March 29, 2021 at 22:17 |
PW144677View Pathway |
drug action
Tigecycline Drug Metabolism Action PathwayHomo sapiens
|
Creator: Ray Kruger Created On: October 07, 2023 at 14:11 Last Updated: October 07, 2023 at 14:11 |
PW146454View Pathway |
drug action
Tilarginine Drug Metabolism Action PathwayHomo sapiens
|
Creator: Ray Kruger Created On: October 07, 2023 at 18:14 Last Updated: October 07, 2023 at 18:14 |
PW132499View Pathway |
Tilbroquinol Drug MetabolismHomo sapiens
Tilbroquinol is a drug that is not metabolized by the human body as determined by current research and biotransformer analysis. Tilbroquinol passes through the liver and is then excreted from the body mainly through the kidney.
|
Creator: Ray Kruger Created On: September 21, 2023 at 22:07 Last Updated: September 21, 2023 at 22:07 |
PW146612View Pathway |
drug action
Tilbroquinol Drug Metabolism Action PathwayHomo sapiens
|
Creator: Ray Kruger Created On: October 07, 2023 at 18:37 Last Updated: October 07, 2023 at 18:37 |
PW146912View Pathway |
drug action
Tilmanocept Drug Metabolism Action PathwayHomo sapiens
|
Creator: Ray Kruger Created On: October 07, 2023 at 19:20 Last Updated: October 07, 2023 at 19:20 |
PW147015View Pathway |
Tiludronate Drug Metabolism PathwayHomo sapiens
|
Creator: Ray Kruger Created On: October 10, 2023 at 13:39 Last Updated: October 10, 2023 at 13:39 |
PW127946View Pathway |
drug action
Tiludronic Acid Action PathwayHomo sapiens
Tiludronic acid is a first-generation bisphosphonate used to treat Paget's disease, similar to etidronic acid and clodronic acid. Tiludronic acid binds to hydroxylapatite in the bone, during bone resorption it is released and taken up by osteoclasts through endocytosis. Once inside the osteoclast, it is released into the cytosol and goes to interrupt osteoclast activity and function. Tiludronic acid has a structure similar to pyrophosphate and due to this can be incorporated into ATP analogues that cannot be hydrolyzed. Due to this the osteoclast cannot utilize ATP and begins to go through apoptosis. If a patient has an overdose they may present with hypocalcemia, which can be treated with supportive care. Tiludronic acid should be taken 2 hours before or after consuming a meal and/or calcium supplements. Avoiding taking it with antacids as it will greatly reduce the bioavailability.
|
Creator: Selena Created On: June 21, 2023 at 13:56 Last Updated: June 21, 2023 at 13:56 |