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
SMILES
Cl.CS(=O)(=O)NCCN1CCC(CCC(=O)C2=C3OCCOC3=C(N)C(Cl)=C2)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
| 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
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10556228
pig 30 mg/kg
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:58:03 GMT 2025
by
admin
on
Mon Mar 31 17:58:03 GMT 2025
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| Record UNII |
M6FO1M266W
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| Record Status |
Validated (UNII)
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C66885
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184159-40-8
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JJ-35
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M6FO1M266W
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300000055241
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DTXSID60939802
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9805251
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CHEMBL303182
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C152449
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