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Details

Stereochemistry RACEMIC
Molecular Formula C19H23N3OS
Molecular Weight 341.47
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEMINOPRAZOLE

SMILES

CC(C)CN(C)C1=C(C[S+]([O-])C2=NC3=C(N2)C=CC=C3)C=CC=C1

InChI

InChIKey=PSIREIZGKQBEEO-UHFFFAOYSA-N
InChI=1S/C19H23N3OS/c1-14(2)12-22(3)18-11-7-4-8-15(18)13-24(23)19-20-16-9-5-6-10-17(16)21-19/h4-11,14H,12-13H2,1-3H3,(H,20,21)

HIDE SMILES / InChI

Molecular Formula C19H23N3OS
Molecular Weight 341.47
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

LEMINOPRAZOLE is an inhibitor of the gastric mucosal proton pump. Its development for the treatment of peptic ulcer was discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
Validity of kissing gastric ulcers induced in rats for screening of antiulcer drugs.
1994
Effects of NC-1300-O-3 on gastric mucus secretion and prostaglandin release in rats.
1994 Aug
Effect on gastric mucus of the proton pump inhibitor leminoprazole and its cytoprotective action against ethanol-induced gastric injury in rats.
1994 Jul
Antisecretory effect of leminoprazole on histamine-stimulated gastric acid secretion in dogs: potent local effect.
1995 Oct
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:31:44 UTC 2023
Edited
by admin
on Sat Dec 16 16:31:44 UTC 2023
Record UNII
59H7G93Y1T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEMINOPRAZOLE
INN  
INN  
Official Name English
LEMINOPRAZOLE [JAN]
Common Name English
NC1300O3
Code English
NC-1300O3
Code English
2-(2-(N-ISOBUTYL-N-METHYLAMINO)BENZYLSULFINYL)BENZIMIDAZOLE
Systematic Name English
BENZENAMINE, 2-((1H-BENZIMIDAZOL-2-YLSULFINYL)METHYL)-N-METHYL-N-(2-METHYLPROPYL)-
Systematic Name English
(±)-2-((O-(ISOBUTYLMETHYLAMINO)BENZYL)SULFINYL)BENZIMIDAZOLE
Common Name English
leminoprazole [INN]
Common Name English
Code System Code Type Description
INN
7002
Created by admin on Sat Dec 16 16:31:44 UTC 2023 , Edited by admin on Sat Dec 16 16:31:44 UTC 2023
PRIMARY
FDA UNII
59H7G93Y1T
Created by admin on Sat Dec 16 16:31:44 UTC 2023 , Edited by admin on Sat Dec 16 16:31:44 UTC 2023
PRIMARY
ChEMBL
CHEMBL2105102
Created by admin on Sat Dec 16 16:31:44 UTC 2023 , Edited by admin on Sat Dec 16 16:31:44 UTC 2023
PRIMARY
SMS_ID
100000082568
Created by admin on Sat Dec 16 16:31:44 UTC 2023 , Edited by admin on Sat Dec 16 16:31:44 UTC 2023
PRIMARY
MESH
C089751
Created by admin on Sat Dec 16 16:31:44 UTC 2023 , Edited by admin on Sat Dec 16 16:31:44 UTC 2023
PRIMARY
CAS
104340-86-5
Created by admin on Sat Dec 16 16:31:44 UTC 2023 , Edited by admin on Sat Dec 16 16:31:44 UTC 2023
PRIMARY
EVMPD
SUB08429MIG
Created by admin on Sat Dec 16 16:31:44 UTC 2023 , Edited by admin on Sat Dec 16 16:31:44 UTC 2023
PRIMARY
PUBCHEM
65881
Created by admin on Sat Dec 16 16:31:44 UTC 2023 , Edited by admin on Sat Dec 16 16:31:44 UTC 2023
PRIMARY
NCI_THESAURUS
C166833
Created by admin on Sat Dec 16 16:31:44 UTC 2023 , Edited by admin on Sat Dec 16 16:31:44 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY