CSP-2503

O=C1CN(CN2CCN(CC2)C3=C4C=CC=CC4=CC=C3)C(=O)[C@@H]5CCCN15

InChIKey=CTZWGZSINBFHFD-FQEVSTJZSA-N

InChI=1S/C22H26N4O2/c27-21-15-25(22(28)20-9-4-10-26(20)21)16-23-11-13-24(14-12-23)19-8-3-6-17-5-1-2-7-18(17)19/h1-3,5-8,20H,4,9-16H2/t20-/m0/s1

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	1 / 1
E/Z Centers	0
Optical Activity	UNSPECIFIED

PubMed

Title	Date	PubMed
Synthesis and structure-activity relationships of a new model of arylpiperazines. 8. Computational simulation of ligand-receptor interaction of 5-HT(1A)R agonists with selectivity over alpha1-adrenoceptors.	2005-04-07	15801844
Anxiolytic-like effect of a serotonergic ligand with high affinity for 5-HT1A, 5-HT2A and 5-HT3 receptors.	2005-03-21	15777774
Design and synthesis of S-(-)-2-[[4-(napht-1-yl)piperazin-1-yl]methyl]-1,4-dioxoperhydropyrrolo[1,2-a]pyrazine (CSP-2503) using computational simulation. A 5-HT1A receptor agonist.	2003-04-17	12668005

Substance Class	Chemical Created by `admin` on `Mon Mar 31 23:18:45 GMT 2025` Edited by `admin` on `Mon Mar 31 23:18:45 GMT 2025`
Record UNII	87UKL3XE5X
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

(-)-CSP-2503

Preferred Name

English

CSP-2503

Common Name

English

PYRROLO(1,2-A)PYRAZINE-1,4-DIONE, HEXAHYDRO-2-((4-(1-NAPHTHALENYL)-1-PIPERAZINYL)METHYL)-, (8AS)-

Systematic Name

English

Code System Code Type Description

EPA CompTox

DTXSID401029560