| Weight | 276.317 g/mol |
|---|---|
| Formula | C13H12N2O3S |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
sulfabenzamide (127-71-9)
benzamide, N-((4-aminophenyl)sulfonyl)-
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- Sigma-Aldrich - sulfabenzamide44.30 - 338.10 USD
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- The Influence of Various Dispersion Methods on the Rate of Dissolution of Sulfabenzamide (Drug Development and Industrial Pharmacy, 1974)
- A systematic study on hydrogen bond interactions in sulfabenzamide: DFT calculations of the N-14, O-17, and H-2 NQR parameters (Biophysical Chemistry, 2009)
- Etude physico-chimique compare des formes I et II du sulfabenzamide (International Journal of Pharmaceutics, 1983)
- Sulfabenzamide promotes autophagic cell death in T-47D breast cancer cells through p53/ DRAM pathway (2012)
- Stable overexpression of DNA fragmentation factor in T-47D cells: sensitization of breast cancer cells to apoptosis in response to acetazolamide and sulfabenzamide (Molecular Biology Reports, 2014)
- [Physico-chemical comparison of two sulfamides: sulfaproxyline and sulfabenzamide]. (Pharmaceutica Acta Helvetiae, 1987)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - benzamide, N-((4-aminophenyl)sulfonyl)-
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SMILESC1=CC=C(C=C1)C(=O)NS(=O)(=O)C2=CC=C(C=C2)N
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InChIKeyPBCZLFBEBARBBI-UHFFFAOYSA-N
- Pubchem - sulfabenzamide
- Wikipedia - sulfabenzamide
Sulfabenzamide is an antibacterial/antimicrobial. Often used in conjunction with sulfathiazole and sulfacetamide (trade name - Sultrin) as a topical, intravaginal antibacterial preparation.
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Similar Compounds
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(68651-46-7, 482-89-3)
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(1083-30-3)
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(80-32-0)
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(101-54-2)
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4 safety hazards
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(842-07-9)
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(530-50-7)
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(842-07-9)
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2 alternate names
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(85-84-7)
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(102-08-9)
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(630-93-3)
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(579-93-1)
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(92-67-1)
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(81-81-2, 127-59-3)
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sulfabenzamide
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