InAADR

Drug Information

Drug Name: deoxycholate (302-95-4)
PubChem ID: 91810855
SMILES: C[C@H](CCC(=O)[O-])[C@H]1CCC2[C@@]1([C@H](CC3[C@H]2CC[C@H]4[C@@]3(CC[C@H](C4)O)C)O)C.[Na+]
InchiKey: FHHPUSMSKHSNKW-WGRCLTAPSA-M
Therapeutic Category:

Computed Drug Properties

Molecular Weight (dalton): 414.562
LogP: 0.1472
Ring Count: 0
Hydrogen Bond Acceptor Count: 4
Hydrogen Bond Donor Count: 2
Total Polar Surface Area: 80.59

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

Interacting drug Toxicity Interaction Type Mechanism Reference

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

Toxicity Interacting Protein Mechanism Reference
Significant Cell Death Inhibition Of Enzymatic Activities Of B16/F10 Melanoma Cells D-dopachrome decarboxylase (P30046) The higher concentrations of antifungal reagent Fungizone (amphotericin B and deoxycholate) caused a significant cell death and the inhibition of enzymatic activities of B16/F10 melanoma cells through activation in dopachrome tautomerase and dopa oxidase activities. [ ADR Type 1 ] Cyclosporine A and prednisone-associated osteoporosis in heart transplant recipients

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