| Description |
An isotope labelled Sulfamethizole. Sulfamethizole is a sulfonamide antibiotic. It competes with PABA to bind to dihydropteroate synthetase to inhibit the synthesis of dihydrofolic acid. |
| Synonyms |
2-Methyl-5-sulfanilamido-1,3,4-thiadiazole-d4; 2-Sulfanilamido-5-methyl-1,3,4-thiadiazole-d4; 4-Amino-N-(5-methyl-[1,3,4]thiadiazol-2-yl)benzenesulfonamide-d4; 5-Methyl-2-sulfanilamido-1,3,4-thiadiazole-d4; Ayerlucil-d4; Famet-d4; Lucosil-d4; Methazol-d4; Microsul-d4; N-(5-Methyl-1,3,4-thiadiazol-2-yl)-4-aminobenzenesulfonamide-d4-d4; N1-(5-Methyl-1,3,4-thiadiazol-2-yl)sulfanilamide-d4; Renasul-d4; Rufol-d4; Salimol-d4; Sulfamethiazole-d4; Sulfamethizol-d4; Sulfamethylthiadiazole-d4; Sulfapyelon-d4; Sulfstat-d4; Sulfurine-d4; Sulphamethizole-d4; Tetracid-d4; Thidicur-d4; Thiosulfil-d4; Thiosulfil Forte-d4; Ultrasul-d4; Urocydal-d4; Urodiaton-d4; Urolucosil-d4; Urosulfin-d4; VK 53-d4; N1-(5-Methyl-1,3,4-thiadiazol-2-yl)sulfanilamide-d4 |
| IUPAC Name |
4-amino-2,3,5,6-tetradeuterio-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide |
| Related CAS |
144-82-1 (unlabelled)
|
| Canonical SMILES |
CC1=NN=C(S1)NS(=O)(=O)C2=CC=C(C=C2)N |
| InChI |
InChI=1S/C9H10N4O2S2/c1-6-11-12-9(16-6)13-17(14,15)8-4-2-7(10)3-5-8/h2-5H,10H2,1H3,(H,12,13)/i2D,3D,4D,5D |
| InChI Key |
VACCAVUAMIDAGB-QFFDRWTDSA-N |
| Purity |
> 95% |
| Solubility |
Soluble in DMSO, Methanol |
| Storage |
Store at -20°C |
![Sulfamethizole-[d4]](https://resource.bocsci.com/structure/2470130-12-0.gif)
