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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H26N4O2
Molecular Weight 378.4674
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CSP-2503

SMILES

[H][C@@]12CCCN1C(=O)CN(CN3CCN(CC3)C4=C5C=CC=CC5=CC=C4)C2=O

InChI

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

HIDE SMILES / InChI

Molecular Formula C22H26N4O2
Molecular Weight 378.4674
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
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 Apr 17
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 Apr 7
Anxiolytic-like effect of a serotonergic ligand with high affinity for 5-HT1A, 5-HT2A and 5-HT3 receptors.
2005 Mar 21
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:32:03 GMT 2023
Edited
by admin
on Sat Dec 16 10:32:03 GMT 2023
Record UNII
87UKL3XE5X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
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
(-)-CSP-2503
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID401029560
Created by admin on Sat Dec 16 10:32:03 GMT 2023 , Edited by admin on Sat Dec 16 10:32:03 GMT 2023
PRIMARY
WIKIPEDIA
CSP-2503
Created by admin on Sat Dec 16 10:32:03 GMT 2023 , Edited by admin on Sat Dec 16 10:32:03 GMT 2023
PRIMARY
PUBCHEM
11291892
Created by admin on Sat Dec 16 10:32:03 GMT 2023 , Edited by admin on Sat Dec 16 10:32:03 GMT 2023
PRIMARY
CAS
581813-10-7
Created by admin on Sat Dec 16 10:32:03 GMT 2023 , Edited by admin on Sat Dec 16 10:32:03 GMT 2023
PRIMARY
FDA UNII
87UKL3XE5X
Created by admin on Sat Dec 16 10:32:03 GMT 2023 , Edited by admin on Sat Dec 16 10:32:03 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY