| Weight | 310.335 g/mol |
|---|---|
| Formula | C12H14N4O4S |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 5 |
sulfadimethoxine (122-11-2, 1037-50-9)
Deposul · Sulphadimethoxine
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#3742 in Chemistry
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- Effect on plants of sulphadimethoxine used in intensive farming (Panicum miliaceum, Pisum sativum and Zea mays) (Agriculture, Ecosystems & Environment, 1995)
- Photochemical Fate of Sulfadimethoxine in Aquaculture Waters (Environmental Science & Technology, 2009)
- Effect of sulphadimethoxine contamination on barley (Hordeum distichum L., Poaceae, Liliposida) (Agriculture, Ecosystems & Environment, 1996)
- Degradation Kinetics of Manure-Derived Sulfadimethoxine in Amended Soil (Journal of Agricultural and Food Chemistry, 2006)
- The structure of the glucuronide of sulphadimethoxine formed in man (Biochemical Journal, 1965)
- Laboratory models to evaluate phytotoxicity of sulphadimethoxine on terrestrial plants (Chemosphere, 1998)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Deposul
- Sulphadimethoxine
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SMILESCOC1=NC(=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N)OC
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- Pubchem - sulfadimethoxine
- Wikipedia - sulfadimethoxine
Sulfadimethoxine (or sulphadimethoxine, trade names Di-Methox or Albon) is a long-lasting sulfonamide antimicrobial medication used in veterinary medicine. It is used to treat many infections, including respiratory, urinary tract, enteric, and soft tissue infections and can be given as a standalone or combined with ormetoprim to broaden the target range. Like all sulfamides, sulfadimethoxine inhibits bacterial synthesis of folic acid by acting as a competitive inhibitor against PABA.
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sulfadimethoxine
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