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Details

Stereochemistry RACEMIC
Molecular Formula C22H23N3O2
Molecular Weight 361.4369
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SERAZAPINE

SMILES

COC(=O)C1=C2C3CN(C)CCN3C4=CC=CC=C4CN2C5=C1C=CC=C5

InChI

InChIKey=WPGUWABWNUSPMW-UHFFFAOYSA-N
InChI=1S/C22H23N3O2/c1-23-11-12-24-17-9-5-3-7-15(17)13-25-18-10-6-4-8-16(18)20(22(26)27-2)21(25)19(24)14-23/h3-10,19H,11-14H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C22H23N3O2
Molecular Weight 361.4369
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Serazapine (CGS15040) is an anxiolytic agent. It is structurally novel 5-HT2 receptor antagonist. Preliminary preclinical findings indicated an anticonflict effect in a behavioral suppression test, and two preliminary investigations in volunteers also suggested anxiolytic potential. In the first of these studies serazapine resembled diazepam, a reference anxiolytic drug, electroencephalographically. Additionally, in a test of psychogenic stress in volunteers it reduced cardiac output.

Approval Year

PubMed

PubMed

TitleDatePubMed
Determination of CGS 15040A in human plasma by liquid chromatography.
1991
Serotonergic (5-HT2) mediation of anxiety-therapeutic effects of serazepine in generalized anxiety disorder.
1993 Jul 1-15
Patents

Sample Use Guides

A double-blind, randomized, placebo-controlled four-compartment parallel group, multicenter trial in outpatients with Generalized Anxiety Disorder (GAD): a 14-to 30-day drug-free interval preceded study entry. For all qualified patients, a 1-week, single-blind placebo washout period was followed by a 5-week, double-blind treatment phase involving a once daily oral dose of either 10 mg, 20 mg, or 40 mg of Serazapine (CGS15040), or placebo. The 40-mg group tended to perform better (larger decreases from baseline in the total Ham-A score) than the other groups.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:39:39 GMT 2023
Edited
by admin
on Fri Dec 15 18:39:39 GMT 2023
Record UNII
8A8FOB4J3U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SERAZAPINE
INN   WHO-DD  
INN  
Official Name English
CPDD-0035
Code English
Serazapine [WHO-DD]
Common Name English
serazapine [INN]
Common Name English
(±)-METHYL 1,3,4,16B-TETRAHYDRO-2-METHYL-2H,10H-INDOLO(2,1-C)PYRAZINO(1,2-A)(1,4)BENZODIAZEPINE-16-CARBOXYLATE
Common Name English
2H,10H-INDOLO(2,1-C)PYRAZINO(1,2-A)(1,4)BENZODIAZEPINE-16-CARBOXYLIC ACID, 1,3,4,16B-TETRAHYDRO-2-METHYL-, METHYL ESTER
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C28197
Created by admin on Fri Dec 15 18:39:39 GMT 2023 , Edited by admin on Fri Dec 15 18:39:39 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID40869592
Created by admin on Fri Dec 15 18:39:39 GMT 2023 , Edited by admin on Fri Dec 15 18:39:39 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110702
Created by admin on Fri Dec 15 18:39:39 GMT 2023 , Edited by admin on Fri Dec 15 18:39:39 GMT 2023
PRIMARY
NCI_THESAURUS
C152340
Created by admin on Fri Dec 15 18:39:39 GMT 2023 , Edited by admin on Fri Dec 15 18:39:39 GMT 2023
PRIMARY
PUBCHEM
60677
Created by admin on Fri Dec 15 18:39:39 GMT 2023 , Edited by admin on Fri Dec 15 18:39:39 GMT 2023
PRIMARY
INN
6576
Created by admin on Fri Dec 15 18:39:39 GMT 2023 , Edited by admin on Fri Dec 15 18:39:39 GMT 2023
PRIMARY
EVMPD
SUB10491MIG
Created by admin on Fri Dec 15 18:39:39 GMT 2023 , Edited by admin on Fri Dec 15 18:39:39 GMT 2023
PRIMARY
SMS_ID
100000084116
Created by admin on Fri Dec 15 18:39:39 GMT 2023 , Edited by admin on Fri Dec 15 18:39:39 GMT 2023
PRIMARY
CAS
115313-22-9
Created by admin on Fri Dec 15 18:39:39 GMT 2023 , Edited by admin on Fri Dec 15 18:39:39 GMT 2023
PRIMARY
FDA UNII
8A8FOB4J3U
Created by admin on Fri Dec 15 18:39:39 GMT 2023 , Edited by admin on Fri Dec 15 18:39:39 GMT 2023
PRIMARY
WIKIPEDIA
Serazapine
Created by admin on Fri Dec 15 18:39:39 GMT 2023 , Edited by admin on Fri Dec 15 18:39:39 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY