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  • ...other chemical groups. A large class of [[antibiotic]]s are based on the sulfonamide structure. Sulfanilamide was the first clinically useful sulfonamide, no longer used due to toxicity. Gerhard Domagk, who was working on antibac
    721 bytes (105 words) - 03:44, 15 November 2010
  • 128 bytes (18 words) - 10:13, 14 March 2009
  • Auto-populated based on [[Special:WhatLinksHere/Sulfonamide]]. Needs checking by a human.
    560 bytes (70 words) - 20:41, 11 January 2010

Page text matches

  • ...p attached to an aniline, no longer used clinically but the first of the [[sulfonamide]] antibiotics
    218 bytes (28 words) - 15:11, 29 April 2009
  • |properties=sulfonamide '''Sulfadiazine''' is an [[antibiotic]] based on the [[sulfonamide]] chemical structure.
    478 bytes (59 words) - 16:15, 14 July 2008
  • ...other chemical groups. A large class of [[antibiotic]]s are based on the sulfonamide structure. Sulfanilamide was the first clinically useful sulfonamide, no longer used due to toxicity. Gerhard Domagk, who was working on antibac
    721 bytes (105 words) - 03:44, 15 November 2010
  • A sulfonamide antibacterial, used as the base or the sodium salt in the treatment of infe
    133 bytes (19 words) - 04:30, 29 April 2009
  • |properties=sulfonamide ...ften called '''4-aminobenzenesulfonamide''', is an [[antibiotic]] of the [[sulfonamide]] class that inhibits bacterial growth by inhibiting the production of foli
    1 KB (161 words) - 03:46, 15 November 2010
  • A [[sulfonamide]] antibacterial agent that interferes with [[folic acid]] synthesis in sus
    272 bytes (35 words) - 14:53, 5 March 2009
  • ...bolism may cause a depression of [[hematopoiesis]]. It is potentiated by [[sulfonamide]]s and the [[trimethoprim-sulfamethoxazole combination]] is the form most o
    438 bytes (55 words) - 17:53, 14 May 2010
  • {{r|Sulfonamide}}
    313 bytes (34 words) - 14:55, 28 May 2009
  • {{r|Sulfonamide}}
    126 bytes (13 words) - 10:11, 14 March 2009
  • Auto-populated based on [[Special:WhatLinksHere/Sulfonamide]]. Needs checking by a human.
    560 bytes (70 words) - 20:41, 11 January 2010
  • ...group(s) with NR<sub>2</sub> - for instance, a [[sulfonic acid]] gives a [[sulfonamide]]. The most important amides are organic amides, derived from [[carboxylic ...he sulfa drugs, the first synthetic [[antibiotic|antibiotics]]), contain a sulfonamide group, and hexamethylphosphoramide (HMPA), the tri-amide of phosphoric acid
    3 KB (410 words) - 02:51, 17 October 2013
  • ...ethyl)-6-propyl-5H-pyran-3-yl]propyl]phenyl]-5-(trifluoromethyl)pyridine-2-sulfonamide and its chemical formula is C<sub>31</sub>H<sub>33</sub>F<sub>3</sub>N<sub>
    1 KB (194 words) - 01:26, 3 June 2009
  • *[[Sulfonamide]]s
    2 KB (280 words) - 23:21, 10 June 2010
  • [[Sulfonamide]]s, (R-SO<sub>2</sub>-NH<sub>2</sub>) are competitive inhibitors of [[para- ...are bacteriostatic rather than bacteriocidal. Bacterial resistance to one sulfonamide indicates resistance to all of them.
    9 KB (1,048 words) - 17:19, 21 March 2024
  • ...with a -SO<sub>3</sub>H group. These [[sulfonic acids]] are used to make [[sulfonamide|sulfa drugs]], and are also strong acids soluble in organic solvents (unlik
    5 KB (750 words) - 22:31, 28 November 2012
  • ...reported, on 21 December 1943, that he had been saved by penicillin; as [[Sulfonamide (medicine)|sulphonamide]] was a [[Germany|German]] discovery, it may be tha
    11 KB (1,713 words) - 07:31, 20 April 2024