| Weight | 249.295 g/mol |
|---|---|
| Formula | C11H11N3O2S |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
sulfapyridine (144-83-2)
Sulphapyridine · Sulphapyridin
Score:
#2576 in Biology
,
#3213 in Chemistry
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- Effect of sulphapyridine, 5-aminosalicylic acid, and placebo in patients with idiopathic proctitis: a study to determine the active therapeutic moiety of sulphasalazine. (Gut, 1980)
- Bullous Pemphigoid Responding to Sulfapyridine and the Sulfones (Archives of Dermatology, 1977)
- Sulphasalazine and sulphapyridine serum levels in children to mothers treated with sulphasalazine during pregnancy and lactation (Acta Paediatrica, 1987)
- Sulfapyridine and Sulfone Type Drugs in Dermatology (Archives of Dermatology, 1962)
- Sulfapyridine appearance in plasma after salicylazosulfapyridine: Another simple measure of intestinal transit*** (Gastroenterology, 1986)
- Placental Transfer of Sulphasalazine and Sulphapyridine and Some of Its Metabolites (Scandinavian Journal of Gastroenterology, 1981)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Sulphapyridine
- Sulphapyridin
-
SMILESC1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N
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InChIKeyGECHUMIMRBOMGK-UHFFFAOYSA-N
- Pubchem - sulfapyridine
- Wikipedia - sulfapyridine
Sulfapyridine, original UK spelling sulphapyridine, is a sulfonamide antibacterial. At one time it was commonly referred to as M&B. Sulfapyridine is no longer prescribed for treatment of infections in humans.
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sulfapyridine
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