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Details

Stereochemistry ABSOLUTE
Molecular Formula C17H27N3O4S
Molecular Weight 369.4807
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ESAMISULPRIDE

SMILES

CCN1CCC[C@@]1([H])CN=C(c2cc(c(cc2OC)N)S(=O)(=O)CC)O

InChI

InChIKey=NTJOBXMMWNYJFB-LBPRGKRZSA-N
InChI=1S/C17H27N3O4S/c1-4-20-8-6-7-12(20)11-19-17(21)13-9-16(25(22,23)5-2)14(18)10-15(13)24-3/h9-10,12H,4-8,11,18H2,1-3H3,(H,19,21)/t12-/m0/s1

HIDE SMILES / InChI

Molecular Formula C17H27N3O4S
Molecular Weight 369.4807
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Amisulpride: a review of its use in the management of schizophrenia.
2004
THE LESSA (Lebanese Short-term Study with Amisulpride) STUDY a Phase IV clinical trial in acutely ill schizophrenic patients.
2004 Apr-Jun
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Jun 26 07:07:26 UTC 2021
Edited
by admin
on Sat Jun 26 07:07:26 UTC 2021
Record UNII
ES3TWM82E8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ESAMISULPRIDE
INN  
Official Name English
AMISULPRIDE, (S)-
Common Name English
ESAMISULPRIDE [INN]
Common Name English
BENZAMIDE, 4-AMINO-N-(((2S)-1-ETHYL-2-PYRROLIDINYL)METHYL)-5-(ETHYLSULFONYL)-2-METHOXY-
Systematic Name English
Code System Code Type Description
PUBCHEM
3055076
Created by admin on Sat Jun 26 07:07:26 UTC 2021 , Edited by admin on Sat Jun 26 07:07:26 UTC 2021
PRIMARY
FDA UNII
ES3TWM82E8
Created by admin on Sat Jun 26 07:07:26 UTC 2021 , Edited by admin on Sat Jun 26 07:07:26 UTC 2021
PRIMARY
NCI_THESAURUS
C175782
Created by admin on Sat Jun 26 07:07:26 UTC 2021 , Edited by admin on Sat Jun 26 07:07:26 UTC 2021
PRIMARY
INN
11322
Created by admin on Sat Jun 26 07:07:26 UTC 2021 , Edited by admin on Sat Jun 26 07:07:26 UTC 2021
PRIMARY
CAS
71675-92-8
Created by admin on Sat Jun 26 07:07:26 UTC 2021 , Edited by admin on Sat Jun 26 07:07:26 UTC 2021
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
TARGET -> INHIBITOR
TARGET -> INHIBITOR
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY