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DILI (Drug-Induced Liver Injury) is liver damage or injury caused by the use of pharmaceutical drugs or medications. DILI can manifest in various forms, ranging from mild elevations in liver enzymes to severe liver failure. The severity of DILI can vary widely from person to person and depends on the individual's genetics and health, and the drug involved. Healthcare providers and researchers closely monitor the capability of drugs to cause DILI, and regulatory agencies have established guidelines for assessing and mitigating this risk during drug development. Understanding and managing DILI is crucial to ensuring the safety of pharmaceuticals and protecting patients from harm.
The Library of Most-DILI-Concern Drugs comprises a selection of pharmaceutical compounds known for their potential to induce liver injury in patients. These drugs have been extensively studied and documented for their hepatotoxic effects. Researchers and healthcare professionals can use this library for in-depth investigations into DILI mechanisms, risk factors, and possible mitigation strategies. It serves as a valuable resource for advancing our understanding of liver-related adverse drug reactions and improving drug safety profiles.
Related terms: H1 receptor, D2 receptor, carbonic anhydrase, acetylcholinesterase, COX-1, epidermal growth factor receptor, D3 receptor.
Mechanism of drug-induced liver injury (Created by BioRender.com)
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NoteAll the compounds with solubility below 10 mM are shipped as 2 mM solutions.
Wnt signaling pathway
9
9
Number of compounds
9
Steroid hormone receptors
6
6
Number of compounds
6
G protein-coupled receptors
6
6
Number of compounds
6
Receptor tyrosine kinases (RTKs)
6
6
Number of compounds
6
Potassium channels
5
5
Number of compounds
5
Eicosanoid turnover
4
4
Number of compounds
4
CD molecules
2
2
Number of compounds
2
RAF family
2
2
Number of compounds
2
Chromatin modifying enzymes
2
2
Number of compounds
2
Catecholamine turnover
2
2
Number of compounds
2
Nuclear hormone receptors
2
2
Number of compounds
2
DNA topoisomerases
2
2
Number of compounds
2
Cytochrome P450
2
2
Number of compounds
2
HIV-1 retropepsin
2
2
Number of compounds
2
Thyroid hormone turnover
2
2
Number of compounds
2
Carbonic anhydrases
2
2
Number of compounds
2
Threonine (T) Peptidases
1
1
Number of compounds
1
Catalytic receptors
1
1
Number of compounds
1
Ligand-gated ion channels
1
1
Number of compounds
1
Voltage-gated ion channels
1
1
Number of compounds
1
P-type ATPases
1
1
Number of compounds
1
Human endogenous retrovirus (HERV) proteins
1
1
Number of compounds
1
Other antimicrobial targets
1
1
Number of compounds
1
enoyl-[acyl-carrier-protein] reductase
1
1
Number of compounds
1
Protein kinase C (PKC) family
1
1
Number of compounds
1
Metallo (M) Peptidases
1
1
Number of compounds
1
Integrase
1
1
Number of compounds
1
Peptidylprolyl isomerase
1
1
Number of compounds
1
SLC22 family of organic cation and anion transporters
1
1
Number of compounds
1
Oxidoreductases
1
1
Number of compounds
1
Adenosine turnover
1
1
Number of compounds
1
Hydrolases
1
1
Number of compounds
1
Aldose reductase
1
1
Number of compounds
1
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