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Details

Stereochemistry ACHIRAL
Molecular Formula C19H28ClN3O5S.ClH
Molecular Weight 482.422
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULAMSEROD HYDROCHLORIDE

SMILES

Cl.CS(=O)(=O)NCCN1CCC(CCC(=O)C2=CC(Cl)=C(N)C3=C2OCCO3)CC1

InChI

InChIKey=JJOQGHGEIKOGPO-UHFFFAOYSA-N
InChI=1S/C19H28ClN3O5S.ClH/c1-29(25,26)22-6-9-23-7-4-13(5-8-23)2-3-16(24)14-12-15(20)17(21)19-18(14)27-10-11-28-19;/h12-13,22H,2-11,21H2,1H3;1H

HIDE SMILES / InChI

Molecular Formula C19H28ClN3O5S
Molecular Weight 445.961
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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

Sulamserod is a methanesulfonamide derivative patented by British multinational pharmaceutical company GlaxoSmithKline as 5-HT4 receptor antagonist, with antiarrhythmic activities for the treatment of the certain cardiovascular condition. 5-HT4 receptor blockade could have antiarrhythmic effects by decreasing intracellular Ca2+ concentration and delayed rectifier potassium current and prolonging atrial refractory period. In preclinical models, Sulamserod prolongs mean atrial effective refractory period and wavelength, reduces the dispersion of effective refractory period, and minimally slows conduction velocity in pigs.

Approval Year

PubMed

PubMed

TitleDatePubMed
Electrophysiological and antiarrhythmic effects of the atrial selective 5-HT(4) receptor antagonist RS-100302 in experimental atrial flutter and fibrillation.
1999 Nov 9
Patents

Patents

Sample Use Guides

pig 30 mg/kg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:26:49 GMT 2023
Edited
by admin
on Fri Dec 15 15:26:49 GMT 2023
Record UNII
M6FO1M266W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULAMSEROD HYDROCHLORIDE
USAN  
USAN  
Official Name English
RS-100302-190
Code English
4-(2-(7-CHLORO-8-AMINO-2,3-DIHYDRO-1,4-BENZODIOXIN-5-YL)CARBONLETHYL-1-YL)-1-(2-(METHYLSULFONAMIDO)ETHYL-1-YL)-PIPERIDINE HYDROCHLORIDE
Common Name English
SULAMSEROD HYDROCHLORIDE [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C66885
Created by admin on Fri Dec 15 15:26:49 GMT 2023 , Edited by admin on Fri Dec 15 15:26:49 GMT 2023
Code System Code Type Description
CAS
184159-40-8
Created by admin on Fri Dec 15 15:26:49 GMT 2023 , Edited by admin on Fri Dec 15 15:26:49 GMT 2023
PRIMARY
USAN
JJ-35
Created by admin on Fri Dec 15 15:26:49 GMT 2023 , Edited by admin on Fri Dec 15 15:26:49 GMT 2023
PRIMARY
FDA UNII
M6FO1M266W
Created by admin on Fri Dec 15 15:26:49 GMT 2023 , Edited by admin on Fri Dec 15 15:26:49 GMT 2023
PRIMARY
EPA CompTox
DTXSID60939802
Created by admin on Fri Dec 15 15:26:49 GMT 2023 , Edited by admin on Fri Dec 15 15:26:49 GMT 2023
PRIMARY
PUBCHEM
9805251
Created by admin on Fri Dec 15 15:26:49 GMT 2023 , Edited by admin on Fri Dec 15 15:26:49 GMT 2023
PRIMARY
ChEMBL
CHEMBL303182
Created by admin on Fri Dec 15 15:26:49 GMT 2023 , Edited by admin on Fri Dec 15 15:26:49 GMT 2023
PRIMARY
NCI_THESAURUS
C152449
Created by admin on Fri Dec 15 15:26:49 GMT 2023 , Edited by admin on Fri Dec 15 15:26:49 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY