InAADR

Drug Information

Drug Name: Irinotecan (97682-44-5)
PubChem ID:
SMILES: CCC1=C2C=C(C=CC2=NC3=C1CN4C3=CC5=C(C4=O)COC(=O)C5(CC)O)OC(=O)N6CCC(CC6)N7CCCCC7
InchiKey: UWKQSNNFCGGAFS-XIFFEERXSA-N
Therapeutic Category: Antineoplastic Agents, Enzyme Inhibitors, Radiation-Sensitizing Agents, Topoisomerase I Inhibitors, Topoisomerase Inhibitors

Computed Drug Properties

Molecular Weight (dalton): 586.689
LogP: 4.0911
Ring Count: 3
Hydrogen Bond Acceptor Count: 9
Hydrogen Bond Donor Count: 1
Total Polar Surface Area: 114.2

This panel provides information on interacting drugs and their ADRs along with references

Interacting drug Toxicity Interaction Type Mechanism Reference
Cyclosporine (59865-13-3) Diarrhea Synergistic The effects of ciclosporin on irinotecan may be due to inhibition of irinotecan and SN-38-related biliary transporters A phase I trial of pharmacologic modulation of irinotecan with cyclosporine and phenobarbital
Oxaliplatin (61825-94-3) Abdominal Pain Synergistic the cholinergic effects of irinotecan, which is a potent inhibitor of acetylcholinesterase, may be enhanced by oxaliplatin Irinotecan-related cholinergic syndrome induced by coadministration of oxaliplatin
Oxaliplatin (61825-94-3) Hypersalivation Synergistic the cholinergic effects of irinotecan, which is a potent inhibitor of acetylcholinesterase, may be enhanced by oxaliplatin Irinotecan-related cholinergic syndrome induced by coadministration of oxaliplatin
St JohnÆs wort (84082-80-4) Reduced Efficacy Antagonistic St John’s wort induces the cytochrome P450 isoenzyme CYP3A4 and P-glycoprotein, which are both involved in the metabolism of irinotecan Effects of St John's wort on irinotecan metabolism

This panel provides drug-protein interaction and their ADRs along with references

Toxicity Interacting Protein Mechanism Reference

This panel provides drug-food interactions and their ADRs along with references

Food Toxicity Reference

This panel provides information on metabolites and their ADRs along with references

Metabolite Toxicity Place of Metabolism Mechanism Reference

This panel provides information on drug category

Toxicity Source

InAADR: Drug-Protein-ADRs database