Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C15H20N2O4S |
| Molecular Weight | 324.395 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CSCCC(NC(C)=O)C(=O)OC1=CC=C(NC(C)=O)C=C1
InChI
InChIKey=GDRGOYFISYGSHQ-UHFFFAOYSA-N
InChI=1S/C15H20N2O4S/c1-10(18)16-12-4-6-13(7-5-12)21-15(20)14(8-9-22-3)17-11(2)19/h4-7,14H,8-9H2,1-3H3,(H,16,18)(H,17,19)
| Molecular Formula | C15H20N2O4S |
| Molecular Weight | 324.395 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Sumacetamol is a acetylaminothioalkanoate derivative patented by Sterwin A.-G. as an analgesic and antipyretic agent. Sumacetamol is used in combination with free paracetamol. In clinical trials, Sumacetamol failed to demonstrate superior efficacy in pain and swelling management compare to paracetamol but shows a longer duration of analgesia. The rates of reported adverse events were similar in paracetamol and Sumacetamol, although reports of mild to moderate drowsiness were more common after the Sumacetamol combination.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3780826
b.i.d. (equivalent to 2 g paracetamol X 2)
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 07:47:03 GMT 2025
by
admin
on
Wed Apr 02 07:47:03 GMT 2025
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| Record UNII |
A0BK6FM64M
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Official Name | English | ||
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Code | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C241
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C75075
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SUB10768MIG
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10041933
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CHEMBL2107605
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273-914-2
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DTXSID90219260
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69217-67-0
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5809
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100000082961
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A0BK6FM64M
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C042733
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |