CHEBI:84119 - triprolidine hydrochloride (anh.)

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ChEBI Name triprolidine hydrochloride (anh.)
ChEBI ID CHEBI:84119
Definition A hydrochloride resulting from the formal reaction of equimolar amounts of triprolidine and hydrogen chloride. Its monohydrate is used for the symptomatic relief of uticaria, rhinitis, and various pruritic skin disorders.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C19H23ClN2
Net Charge 0
Average Mass 314.85200
Monoisotopic Mass 314.15498
InChI InChI=1S/C19H22N2.ClH/c1-16-7-9-17(10-8-16)18(19-6-2-3-12-20-19)11-15-21-13-4-5-14-21;/h2-3,6-12H,4-5,13-15H2,1H3;1H/b18-11+;
InChIKey WYUYEJNGHIOFOC-NWBUNABESA-N
SMILES Cl.Cc1ccc(cc1)C(=C/CN1CCCC1)\c1ccccn1
Roles Classification
Biological Role(s): H1-receptor antagonist
H1-receptor antagonists are the drugs that selectively bind to but do not activate histamine H1 receptors, thereby blocking the actions of endogenous histamine.
Application(s): H1-receptor antagonist
H1-receptor antagonists are the drugs that selectively bind to but do not activate histamine H1 receptors, thereby blocking the actions of endogenous histamine.
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ChEBI Ontology
Outgoing triprolidine hydrochloride (anh.) (CHEBI:84119) has part triprolidine(1+) (CHEBI:84117)
triprolidine hydrochloride (anh.) (CHEBI:84119) has role H1-receptor antagonist (CHEBI:37955)
triprolidine hydrochloride (anh.) (CHEBI:84119) is a hydrochloride (CHEBI:36807)
Incoming triprolidine hydrochloride monohydrate (CHEBI:32265) has part triprolidine hydrochloride (anh.) (CHEBI:84119)
IUPAC Name
2-[(1E)-1-(4-methylphenyl)-3-(pyrrolidin-1-yl)prop-1-en-1-yl]pyridine hydrochloride
Synonyms Sources
1-[(2E)-3-(4-methylphenyl)-3-(pyridin-2-yl)prop-2-en-1-yl]pyrrolidinium chloride IUPAC
triprolidine hydrochloride (anhydrous) ChEBI
triprolidine hydrochloride anhydrous ChemIDplus
triprolidine monohydrochloride (anh.) ChEBI
triprolidine monohydrochloride (anhydrous) ChEBI
triprolidine monohydrochloride anhydrous ChEBI
Registry Numbers Types Sources
3743215 Reaxys Registry Number Reaxys
550-70-9 CAS Registry Number ChemIDplus
Last Modified
17 December 2014