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Details

Stereochemistry RACEMIC
Molecular Formula C14H22ClN3O3S
Molecular Weight 347.861
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LORAPRIDE

SMILES

CCN1CCCC1CNS(=O)(=O)C2=C(OC)C=C(N)C(Cl)=C2

InChI

InChIKey=YSWVLPFCGJOQQA-UHFFFAOYSA-N
InChI=1S/C14H22ClN3O3S/c1-3-18-6-4-5-10(18)9-17-22(19,20)14-7-11(15)12(16)8-13(14)21-2/h7-8,10,17H,3-6,9,16H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C14H22ClN3O3S
Molecular Weight 347.861
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Lorapride is a centrally acting sulfonamide. It has pharmacodynamic properties that are mainly related to ulcer treatment. On the basis of its psychopharmacologic profile, it has no neuroleptic potential, but it does exhibit some psychostimulating components. After oral administration, absorption of lorapride was rapid. The rate of absorption was first order for solution and zero order for capsule.

Approval Year

PubMed

PubMed

TitleDatePubMed
Quantitative thin-layer and high-performance liquid chromatographic determination of lorapride in biological fluids and a pharmacokinetic study in humans.
1985 Nov
Patents

Sample Use Guides

Single dose - 100 mg
Route of Administration: Other
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:56:32 GMT 2023
Edited
by admin
on Sat Dec 16 16:56:32 GMT 2023
Record UNII
549TIC7B4R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LORAPRIDE
INN  
INN  
Official Name English
lorapride [INN]
Common Name English
5-CHLORO-N1-((1-ETHYL-2-PYRROLIDINYL)METHYL)-2-METHOXYSULFANILAMIDE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29701
Created by admin on Sat Dec 16 16:56:32 GMT 2023 , Edited by admin on Sat Dec 16 16:56:32 GMT 2023
Code System Code Type Description
PUBCHEM
68881
Created by admin on Sat Dec 16 16:56:32 GMT 2023 , Edited by admin on Sat Dec 16 16:56:32 GMT 2023
PRIMARY
INN
4909
Created by admin on Sat Dec 16 16:56:32 GMT 2023 , Edited by admin on Sat Dec 16 16:56:32 GMT 2023
PRIMARY
CAS
68677-06-5
Created by admin on Sat Dec 16 16:56:32 GMT 2023 , Edited by admin on Sat Dec 16 16:56:32 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105073
Created by admin on Sat Dec 16 16:56:32 GMT 2023 , Edited by admin on Sat Dec 16 16:56:32 GMT 2023
PRIMARY
NCI_THESAURUS
C81599
Created by admin on Sat Dec 16 16:56:32 GMT 2023 , Edited by admin on Sat Dec 16 16:56:32 GMT 2023
PRIMARY
MESH
C047748
Created by admin on Sat Dec 16 16:56:32 GMT 2023 , Edited by admin on Sat Dec 16 16:56:32 GMT 2023
PRIMARY
FDA UNII
549TIC7B4R
Created by admin on Sat Dec 16 16:56:32 GMT 2023 , Edited by admin on Sat Dec 16 16:56:32 GMT 2023
PRIMARY
EPA CompTox
DTXSID50867706
Created by admin on Sat Dec 16 16:56:32 GMT 2023 , Edited by admin on Sat Dec 16 16:56:32 GMT 2023
PRIMARY
SMS_ID
100000082011
Created by admin on Sat Dec 16 16:56:32 GMT 2023 , Edited by admin on Sat Dec 16 16:56:32 GMT 2023
PRIMARY
EVMPD
SUB08580MIG
Created by admin on Sat Dec 16 16:56:32 GMT 2023 , Edited by admin on Sat Dec 16 16:56:32 GMT 2023
PRIMARY
ECHA (EC/EINECS)
272-057-1
Created by admin on Sat Dec 16 16:56:32 GMT 2023 , Edited by admin on Sat Dec 16 16:56:32 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY