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03. Biological Effects of Specific Chemicals
03. Biological Effects of Specific Chemicals
aclidinium [CHEBI:65346] (1)
05. Industrial Uses
05. Industrial Uses
aclidinium [CHEBI:65346] (1)
08. Chemical Category
08. Chemical Category
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
aclidinium [CHEBI:65346] (1)
ChEBI Compound Accession Identifier :
[CHEBI:65346]
ChEBI Compound Description :
A carboxylic ester obtained by formal condensation between the carboxy group of 2-hydroxy(di-2-thienyl)acetic acid and the hydroxy group of N-(3-phenoxypropyl)-3-quinuclidinol. Used as its bromide salt for the long-term maintenance treatment of bronchospasm associated with chronic obstructive pulmonary disease (COPD).
ChEBI Compound Identification Number :
65346
ChEBI InChI Value :
InChI=1S/C26H30NO4S2/c28-25(26(29,23-9-4-17-32-23)24-10-5-18-33-24)31-22-19-27(14-11-20(22)12-15-27)13-6-16-30-21-7-2-1-3-8-21/h1-5,7-10,17-18,20,22,29H,6,11-16,19H2/q+1/t20?,22-,27?/m0/s1
ChEBI InChIKey Value :
ASMXXROZKSBQIH-VITNCHFBSA-N
ChEBI Compound Name :
aclidinium
ChEBI SMILES Value :
OC(C(=O)O[C@H]1C[N+]2(CCCOc3ccccc3)CCC1CC2)(c1cccs1)c1cccs1
ChEBI Substance ID :
160644942
ChEBI URL :
ChEBI:65346
ChemSpider ID :
9609381
Ontomatica Chemical Accession Key (OnChAKey) :
ASMXXROZKSBQIH_VITNCHFBSA_N_000_000000
PubChem Compound ID :
11434515