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Details

Stereochemistry ABSOLUTE
Molecular Formula C15H23N3O4S.ClH
Molecular Weight 377.887
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULPIRIDE HYDROCHLORIDE, (R)-

SMILES

Cl.CCN1CCC[C@@H]1CNC(=O)C2=CC(=CC=C2OC)S(N)(=O)=O

InChI

InChIKey=PFHZICSPLHQCDZ-RFVHGSKJSA-N
InChI=1S/C15H23N3O4S.ClH/c1-3-18-8-4-5-11(18)10-17-15(19)13-9-12(23(16,20)21)6-7-14(13)22-2;/h6-7,9,11H,3-5,8,10H2,1-2H3,(H,17,19)(H2,16,20,21);1H/t11-;/m1./s1

HIDE SMILES / InChI

Molecular Formula C15H23N3O4S
Molecular Weight 341.426
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Identification and pharmacological characterization of [125I]L-750,667, a novel radioligand for the dopamine D4 receptor.
1996-12
Expression and pharmacological characterization of the human D3 dopamine receptor.
1994-01
Unique binding characteristics of antipsychotic agents interacting with human dopamine D2A, D2B, and D3 receptors.
1993-05
Molecular cloning and characterization of a novel dopamine receptor (D3) as a target for neuroleptics.
1990-09-13
Substance Class Chemical
Created
by admin
on Tue Apr 01 16:31:40 GMT 2025
Edited
by admin
on Tue Apr 01 16:31:40 GMT 2025
Record UNII
9964K1S45E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BENZAMIDE, 5-(AMINOSULFONYL)-N-(((2R)-1-ETHYL-2-PYRROLIDINYL)METHYL)-2-METHOXY-, HYDROCHLORIDE (1:1)
Preferred Name English
SULPIRIDE HYDROCHLORIDE, (R)-
Common Name English
Code System Code Type Description
FDA UNII
9964K1S45E
Created by admin on Tue Apr 01 16:31:40 GMT 2025 , Edited by admin on Tue Apr 01 16:31:40 GMT 2025
PRIMARY
PUBCHEM
119026019
Created by admin on Tue Apr 01 16:31:40 GMT 2025 , Edited by admin on Tue Apr 01 16:31:40 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER