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> Main
CHEBI:31866 - mosapramine dihydrochloride
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ChEBI Name
mosapramine dihydrochloride
ChEBI ID
CHEBI:31866
Definition
A racemate comprising equimolar amounts of (
R
)- and (
S
)-mosapramine dihydrochloride.
Stars
This entity has been manually annotated by a third party.
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Formulae
C28H35ClN4O.2HCl
C28H35ClN4O.ClH.ClH
Net Charge
0
Average Mass
551.980
Monoisotopic Mass
550.20329
InChI
InChI=1S/C28H35ClN4O.2ClH/c29-
23-
12-
11-
22-
10-
9-
21-
6-
1-
2-
7-
24(21)
32(25(22)
20-
23)
16-
5-
15-
31-
18-
13-
28(14-
19-
31)
27(34)
30-
26-
8-
3-
4-
17-
33(26)
28;;/h1-
2,6-
7,11-
12,20,26H,3-
5,8-
10,13-
19H2,(H,30,34)
;2*1H
InChIKey
CVCDAZZJQWLXHM-UHFFFAOYSA-N
SMILES
Cl.Cl.ClC1=CC=C2CCC3=CC=CC=C3N(CCCN3CCC4(CC3)N3CCCCC3NC4=O)C2=C1
Roles Classification
Biological Role
(s):
dopaminergic antagonist
A drug that binds to but does not activate dopamine receptors, thereby blocking the actions of dopamine or exogenous agonists.
Application
(s):
dopaminergic antagonist
A drug that binds to but does not activate dopamine receptors, thereby blocking the actions of dopamine or exogenous agonists.
second generation antipsychotic
Antipsychotic drugs which can have different modes of action but which tend to be less likely than first generation antipsychotics to cause extrapyramidal motor control disabilities such as body rigidity or Parkinson's disease-type movements.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
mosapramine dihydrochloride (
CHEBI:31866
)
has role
dopaminergic antagonist (
CHEBI:48561
)
mosapramine dihydrochloride (
CHEBI:31866
)
has role
second generation antipsychotic (
CHEBI:65191
)
mosapramine dihydrochloride (
CHEBI:31866
)
is a
racemate (
CHEBI:60911
)
IUPAC Name
rac
-
1'-
[3-
(3-
chloro-
10,11-
dihydro-
5
H
-
dibenzo[
b
,
f
]azepin-
5-
yl)propyl]hexahydro-
2
H
-
spiro[imidazo[1,2-
a
]pyridine-
3,4'-
piperidin]-
2-
one dihydrochloride
Synonyms
Sources
Cremin
KEGG DRUG
mosapramine .2HCl
ChEBI
mosapramine dihydrochloride
KEGG DRUG
mosapramine hydrochloride
ChemIDplus
Manual Xref
Database
D01548
KEGG DRUG
View more database links
Registry Number
Type
Source
98043-60-8
CAS Registry Number
ChemIDplus
Citations
Types
Sources
8103712
PubMed citation
Europe PMC
8690306
PubMed citation
Europe PMC
Last Modified
14 January 2021