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Details

Stereochemistry ACHIRAL
Molecular Formula C25H24F2N4OS
Molecular Weight 466.546
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NRA-0562

SMILES

NC(=O)C1=NC(=C(CCN2CCC(CC2)C3=CNC4=C3C=CC(F)=C4)S1)C5=CC=C(F)C=C5

InChI

InChIKey=KGCLWPBGLDFQHP-UHFFFAOYSA-N
InChI=1S/C25H24F2N4OS/c26-17-3-1-16(2-4-17)23-22(33-25(30-23)24(28)32)9-12-31-10-7-15(8-11-31)20-14-29-21-13-18(27)5-6-19(20)21/h1-6,13-15,29H,7-12H2,(H2,28,32)

HIDE SMILES / InChI

Molecular Formula C25H24F2N4OS
Molecular Weight 466.546
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Antipsychotic action of selective group II metabotropic glutamate receptor agonist MGS0008 and MGS0028 on conditioned avoidance responses in the rat.
2003-08-15
In vitro and in vivo pharmacological profile of 5-[2-[4-(6-fluoro-1H-indole-3-yl)piperidin-1-yl]ethyl]-4-(4-fluorophenyl)thiazole-2-carboxylic acid amide (NRA0562), a novel and putative atypical antipsychotic.
2002-08-09
Antipsychotic profile of 5-[2-[4-(6-fluoro-1H-indole-3-yl)piperidin-1-yl]ethyl]-4-(4-fluorophenyl)thiazole-2-carboxylic acid amide (NRA0562) in rats.
2002-07-12
Neuropharmacological profiles of a novel atypical antipsychotic, NRA0562, in rats.
2001-06-29
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:49:32 GMT 2025
Edited
by admin
on Mon Mar 31 22:49:32 GMT 2025
Record UNII
Z2684U429S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NRA-0562
Common Name English
2-THIAZOLECARBOXAMIDE, 5-(2-(4-(6-FLUORO-1H-INDOL-3-YL)-1-PIPERIDINYL)ETHYL)-4-(4-FLUOROPHENYL)-
Preferred Name English
Code System Code Type Description
CAS
244276-65-1
Created by admin on Mon Mar 31 22:49:32 GMT 2025 , Edited by admin on Mon Mar 31 22:49:32 GMT 2025
PRIMARY
PUBCHEM
9804574
Created by admin on Mon Mar 31 22:49:32 GMT 2025 , Edited by admin on Mon Mar 31 22:49:32 GMT 2025
PRIMARY
FDA UNII
Z2684U429S
Created by admin on Mon Mar 31 22:49:32 GMT 2025 , Edited by admin on Mon Mar 31 22:49:32 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY