Drug Name: | Candesartan (139481-59-7) |
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PubChem ID: | 2541 |
SMILES: | CCOC1=NC2=CC=CC(=C2N1CC3=CC=C(C=C3)C4=CC=CC=C4C5=NNN=N5)C(=O)O |
InchiKey: | HTQMVQVXFRQIKW-UHFFFAOYSA-N |
Therapeutic Category: | Angiotensin II Type 1 Receptor Blockers, Angiotensin Receptor Antagonists, Antihypertensive Agents, Cardiovascular Agents |
Molecular Weight (dalton) | : | 440.463 |
LogP | : | 4.0286 |
Ring Count | : | 5 |
Hydrogen Bond Acceptor Count | : | 7 |
Hydrogen Bond Donor Count | : | 2 |
Total Polar Surface Area | : | 118.81 |
This panel provides information on interacting drugs and their ADRs along with references
Interacting drug | Toxicity | Interaction Type | Mechanism | Reference |
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Spironolactone (52-01-7) | Hyperkalaemia | Antagonistic | Candesartan reduces the levels of aldosterone, which results in the retention of potassium | Interaction of spironolactone with ACE inhibitors or angiotensin receptor blockers: analysis of 44 cases |
This panel provides drug-protein interaction and their ADRs along with references
Toxicity | Interacting Protein | Mechanism | Reference |
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This panel provides drug-food interactions and their ADRs along with references
Food | Toxicity | Reference |
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This panel provides information on metabolites and their ADRs along with references
Metabolite | Toxicity | Place of Metabolism | Mechanism | Reference |
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This panel provides information on drug category