CHEBI ONTOLOGY - ANNOTATIONS
The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at http://www.ebi.ac.uk/chebi/ . The data is made available under the Creative Commons License (CC BY 3.0, http://creativecommons.org/licenses/by/3.0/ ). For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.
Term: tiquizium bromide
Accession: CHEBI:32232
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Definition: A organic bromide salt of tiquizium. It is an antispasmodic drug used for the treatment of convulsion and hypermobility in gastritis, gastric ulcer, duodenal ulcer, enteritis, irritable bowel syndrome, gallbladder disease, biliary tract disease and urolithiasis.
Synonyms: exact_synonym: (5R,9aR)-3-[di(thiophen-2-yl)methylidene]-5-methyloctahydro-2H-quinolizinium bromide
related_synonym: (5R,9aR)-3-[di(thiophen-2-yl)methylidene]-5-methyloctahydro-2H-quinolizin-5-ium bromide; 3-(di(2-thienyl)methylene)-5-methyldecahydroquinolizinium bromide; 3-(di-2-thienylmethylene)-5-methyl-trans-quinolizidinium bromide; Advaston; Aspora; Breiful; Formula=C19H24NS2.Br; Gastirol; HSR 902; InChI=1S/C19H24NS2.BrH/c1-20-11-3-2-6-16(20)10-9-15(14-20)19(17-7-4-12-21-17)18-8-5-13-22-18;/h4-5,7-8,12-13,16H,2-3,6,9-11,14H2,1H3;1H/q+1;/p-1/t16-,20-;/m1./s1; InChIKey=VKBNGRDAHSELMQ-KYSFMIDTSA-M; SMILES=C(=C1C[N@+]2(C)[C@@](CC1)(CCCC2)[H])(C3=CC=CS3)C4=CC=CS4.[Br-]; Thiameron; Thiaton; Thiwan; Tiapaston; bromure de tiquizium; bromuro de tiquizio; tiquizii bromidum; trans-3-(di-2-thienylmethylene)octahydro-5-methyl-2H-quinolizinium bromide
xref: CAS:71731-58-3; Drug_Central:2678; KEGG:D01875
xref_mesh: MESH:C030950
xref: PMID:10475017; PMID:11855677; PMID:2881461; PMID:2895053; PMID:2895054; PMID:3656779; PMID:4090525; PMID:6120131; PMID:6277751; PMID:6631675; PMID:6677720; PMID:7262709; PMID:7302972; PMID:8839659
G
Kcnh2
potassium voltage-gated channel subfamily H member 2
decreases activity
ISO
thiaton results in decreased activity of KCNH2 protein
CTD
PMID:28551711
NCBI chr 4:10,826,834...10,859,009
Ensembl chr 4:10,826,928...10,859,008
G
Mpo
myeloperoxidase
multiple interactions
EXP
thiaton inhibits the reaction [Indomethacin results in increased activity of MPO protein]
CTD
PMID:11855677
NCBI chr10:72,594,458...72,608,862
Ensembl chr10:72,594,661...72,604,819
G
Nos2
nitric oxide synthase 2
multiple interactions
EXP
thiaton inhibits the reaction [Indomethacin results in increased activity of NOS2 protein]
CTD
PMID:11855677
NCBI chr10:63,815,308...63,851,208
Ensembl chr10:63,815,308...63,851,210
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