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Pathways

PathWhiz ID Pathway Meta Data

PW175940

Pw175940 View Pathway
metabolic

Ticlopidine Predicted Metabolism Pathway

Homo sapiens
Ticlopidine PIS1M1, Ticlopidine PIS1M2, Ticlopidine PIS1M3,Ticlopidine PIS1M4, Ticlopidine PIS2M1, Ticlopidine PIS2M2, Ticlopidine PIS2M3 are metabolites of Ticlopidine predicted with biotransformer.

PW000689

Pw000689 View Pathway
drug action

Tigecycline Action Pathway

Homo 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.

PW124612

Pw124612 View Pathway
drug action

Tigecycline Anti-bacterial Action Pathway

Homo 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.

PW144677

Pw144677 View Pathway
drug action

Tigecycline Drug Metabolism Action Pathway

Homo sapiens

PW146454

Pw146454 View Pathway
drug action

Tilarginine Drug Metabolism Action Pathway

Homo sapiens

PW132499

Pw132499 View Pathway
metabolic

Tilbroquinol Drug Metabolism

Homo 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.

PW146612

Pw146612 View Pathway
drug action

Tilbroquinol Drug Metabolism Action Pathway

Homo sapiens

PW146912

Pw146912 View Pathway
drug action

Tilmanocept Drug Metabolism Action Pathway

Homo sapiens

PW147015

Pw147015 View Pathway
metabolic

Tiludronate Drug Metabolism Pathway

Homo sapiens

PW127946

Pw127946 View Pathway
drug action

Tiludronic Acid Action Pathway

Homo 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.