38006-08-5
Chemical Structure
Sulfamonomethoxine sodium
- CAS. Nr.: 38006-08-5
- Formula:C11H11N4NaO3S
- Molecular Weight:302.29
IUPAC Name: sodium ((4-aminophenyl)sulfonyl)(6-methoxypyrimidin-4-yl)amide
InChIKey: IZJAOWYNDLDRKM-UHFFFAOYSA-N
SMILES: COC1=NC=NC(=C1)[N-]S(=O)(=O)C2=CC=C(C=C2)N.[Na+]
Biological Activity: Sulfamonomethoxine sodium is an orally active broad-spectrum synthetic sulfonamide antibiotic that inhibits dihydropteroate synthetase. Sulfamonomethoxine sodium increases blood glucose levels, induces anxiety-related activities and impairs spatial learning and memory. Sulfamonomethoxine sodium can be used for the research of anxiety, spatial memory impairment, colisepticemia, salmonellosis, and staphylococcus infection[1][2][3].
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Sulfamonomethoxine sodium | 99.88% | Sulfamonomethoxine sodium is an orally active broad-spectrum synthetic sulfonamide antibiotic that inhibits dihydropteroate synthetase. Sulfamonomethoxine sodium increases blood glucose levels, induces anxiety-related activities and impairs spatial learning and memory. Sulfamonomethoxine sodium can be used for the research of anxiety, spatial memory impairment, colisepticemia, salmonellosis, and staphylococcus infection. | ||||||||||||||||||||
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Sulfamonomethoxine sodium (Standard) | ≥98% | Sulfamonomethoxine sodium (Standard) is the analytical standard of Sulfamonomethoxine sodium. This product is intended for research and analytical applications. Sulfamonomethoxine sodium is an orally active broad-spectrum synthetic sulfonamide antibiotic that inhibits dihydropteroate synthetase. Sulfamonomethoxine sodium increases blood glucose levels, induces anxiety-related activities and impairs spatial learning and memory. Sulfamonomethoxine sodium can be used for the research of anxiety, spatial memory impairment, colisepticemia, salmonellosis, and staphylococcus infection. | ||||||||||||||||||||
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- [1]. Zhang Q, et al. Physiological and behavioral responses in offspring mice following maternal exposure to sulfamonomethoxine during pregnancy. Neurosci Lett. 2016;624:8-16. [Content Brief]
- [2]. Bilandžić N, et al. Distribution of sulfamonomethoxine and trimethoprim in egg yolk and white. Food Chem. 2015;178:32-37. [Content Brief]
- [3]. Huang DJ, et al. Toxicity of the veterinary sulfonamide antibiotic sulfamonomethoxine to five aquatic organisms. Environ Toxicol Pharmacol. 2014;38(3):874-880. [Content Brief]
