CHEBI:2669 - amlodipine benzenesulfonate

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ChEBI Name amlodipine benzenesulfonate
Definition The benzenesulfonate salt of amlodipine.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formulae C20H25ClN2O5.C6H6O3S
Net Charge 0
Average Mass 567.05100
Monoisotopic Mass 566.14896
InChI InChI=1S/C20H25ClN2O5.C6H6O3S/c1-4-28-20(25)18-15(11-27-10-9-22)23-12(2)16(19(24)26-3)17(18)13-7-5-6-8-14(13)21;7-10(8,9)6-4-2-1-3-5-6/h5-8,17,23H,4,9-11,22H2,1-3H3;1-5H,(H,7,8,9)
SMILES OS(=O)(=O)c1ccccc1.CCOC(=O)C1=C(COCCN)NC(C)=C(C1c1ccccc1Cl)C(=O)OC
Roles Classification
Biological Role(s): calcium channel blocker
One of a class of drugs that acts by selective inhibition of calcium influx through cell membranes or on the release and binding of calcium in intracellular pools.
Application(s): vasodilator agent
A drug used to cause dilation of the blood vessels.
antihypertensive agent
Any drug used in the treatment of acute or chronic vascular hypertension regardless of pharmacological mechanism.
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ChEBI Ontology
Outgoing amlodipine benzenesulfonate (CHEBI:2669) has part amlodipine (CHEBI:2668)
amlodipine benzenesulfonate (CHEBI:2669) has role antihypertensive agent (CHEBI:35674)
amlodipine benzenesulfonate (CHEBI:2669) has role calcium channel blocker (CHEBI:38215)
amlodipine benzenesulfonate (CHEBI:2669) has role vasodilator agent (CHEBI:35620)
amlodipine benzenesulfonate (CHEBI:2669) is a organosulfonate salt (CHEBI:64382)
Incoming Prestalia (CHEBI:85999) has part amlodipine benzenesulfonate (CHEBI:2669)
3-ethyl 5-methyl 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate benzenesulfonate
INNs Sources
amlodipine ChEBI
amlodipino DrugBank
amlodipinum DrugBank
Synonyms Sources
Amlodipine besilate KEGG DRUG
Amlodipine besylate KEGG DRUG
Manual Xrefs Databases
DB00381 DrugBank
View more database links
Registry Numbers Types Sources
111470-99-6 CAS Registry Number ChemIDplus
111470-99-6 CAS Registry Number KEGG DRUG
8378713 Beilstein Registry Number Beilstein
Last Modified
11 June 2015