EMBL-EBI | Chemical Biology | ChEBI

Example searches: iron*, InChI=1S/CH4O/c1-2/h2H,1H3, caffeine | Advanced Search

CHEBI:53771 - (R)-aceprometazine

ChEBI IDCHEBI:53771
ChEBI Name(R)-aceprometazine
Stars
ASCII Name(R)-aceprometazine
DefinitionThe (R)-enantiomer of aceprometazine.
Last Modified24 August 2012
SubmitterSteve
DownloadsMolfile
FormulaC19H22N2OS
Net Charge0
Average Mass326.465
Monoisotopic Mass326.14528
SMILESCC(=O)c1ccc2c(c1)N(C[C@@H](C)N(C)C)c1ccccc1S2
InChIInChI=1S/C19H22N2OS/c1-13(20(3)4)12-21-16-7-5-6-8-18(16)23-19-10-9-15(14(2)22)11-17(19)21/h5-11,13H,12H2,1-4H3/t13-/m1/s1
InChIKeyXLOQNFNTQIRSOX-CYBMUJFWSA-N
Roles Classification
Chemical Roles:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Biological Role:
histamine antagonist  Histamine antagonists are the drugs that bind to but do not activate histamine receptors, thereby blocking the actions of histamine or histamine agonists.
Applications:
anxiolytic drug  Anxiolytic drugs are agents that alleviate anxiety, tension, and anxiety disorders, promote sedation, and have a calming effect without affecting clarity of consciousness or neurologic conditions.
histamine antagonist  Histamine antagonists are the drugs that bind to but do not activate histamine receptors, thereby blocking the actions of histamine or histamine agonists.
sedative  A central nervous system depressant used to induce drowsiness or sleep or to reduce psychological excitement or anxiety.
ChEBI Ontology
Outgoing Relation(s)
(R)-aceprometazine (CHEBI:53771) is a aceprometazine (CHEBI:53770)
(R)-aceprometazine (CHEBI:53771) is enantiomer of (S)-aceprometazine (CHEBI:53772)
Incoming Relation(s)
(S)-aceprometazine (CHEBI:53772) is enantiomer of (R)-aceprometazine (CHEBI:53771)
IUPAC Name 
1-{10-[(2R)-2-(dimethylamino)propyl]-10H-phenothiazin-2-yl}ethanone