Weight | 255.324 g/mol |
---|---|
Formula | C9H9N3O2S2 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 3 |
sulfathiazole (72-14-0)
Alphadol · N(1)-2-thiazolylsulfanilamide · norsulfazole
Score:
#932 in Biology
,
#1030 in Chemistry
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- Studies on Absorption of Eutectic Mixture. I. A Comparison of the Behavior of Eutectic Mixture of Sulfathiazole and that of Ordinary Sulfathiazole in Man. (Chemical & Pharmaceutical Bulletin, 1961)
- Dissolution Rates of High Energy Polyvinylpyrrolidone (PVP)-Sulfathiazole Coprecipitates (Journal of Pharmaceutical Sciences, 1969)
- Evaluating the biodegradability of sulfamethazine, sulfamethoxazole, sulfathiazole, and trimethoprim at different stages of sewage treatment (Environmental Toxicology and Chemistry, 2005)
- Inhibition of Sulfathiazole Crystal Growth by Polyvinylpyrrolidone (Journal of Pharmaceutical Sciences, 1970)
- Over one hundred solvates of sulfathiazole (Chemical Communications, 2001)
- Dissolution rates of high energy sulfathiazole-povidone coprecipitates II: Characterization of form of drug controlling its dissolution rate via solubility studies (Journal of Pharmaceutical Sciences, 1976)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Alphadol
- N(1)-2-thiazolylsulfanilamide
- norsulfazole
- sulfathiazole, monosodium salt
-
SMILESC1=CC(=CC=C1N)S(=O)(=O)NC2=NC=CS2
-
InChIKeyJNMRHUJNCSQMMB-UHFFFAOYSA-N
- Pubchem - sulfathiazole
- Wikipedia - sulfathiazole
Sulfathiazole is an organosulfur compound used as a short-acting sulfa drug. It is an organic compound. Formerly, it was a common oral and topical antimicrobial, until less toxic alternatives were discovered.
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