Sulfanilamide: Difference between revisions

Jump to navigation Jump to search
Line 5: Line 5:
{{CMG}}; {{AE}} {{MM}}
{{CMG}}; {{AE}} {{MM}}
==Overview==
==Overview==
'''Sulfanilamide''' (also spelled '''sulphanilamide''') is a [[sulfonamide (medicine)|sulfonamide]] [[antibacterial]]. Chemically, it is a molecule containing the [[Sulfonamide (chemistry)|sulfonamide]] functional group attached to an [[aniline]].
Sulfanilamide was first prepared in 1908 by Paul Gelmo as part of his dissertation for a doctoral degree from the Technische Hochsschule of Vienna, Austria.<ref>Paul Gelmo (May 14, 1908) [http://gallica.bnf.fr/ark:/12148/bpt6k90849c/f378.image "Über Sulfamide der p-Amidobenzolsulfonsäure,"] ''Journal für Praktische Chemie'', '''77''' :  369-382.</ref>  It was patented in 1909.<ref>On May 18, 1909, Deutsches Reich Patentschrift number 226,239 for sulfanilamide was awarded to Heinrich Hörlein of the Bayer corporation.</ref>


==Category==
==Category==

Revision as of 08:36, 9 January 2014

Sulfanilamide
AVC VAGINAL® FDA Package Insert
Description
Clinical Pharmacology
Indications and Usage
Contraindications
Warnings and Precautions
Adverse Reactions
Overdosage
Dosage and Administration
How Supplied
Labels and Packages

For patient information, click here.

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mohamed Moubarak, M.D. [2]

Overview

Sulfanilamide (also spelled sulphanilamide) is a sulfonamide antibacterial. Chemically, it is a molecule containing the sulfonamide functional group attached to an aniline.

Sulfanilamide was first prepared in 1908 by Paul Gelmo as part of his dissertation for a doctoral degree from the Technische Hochsschule of Vienna, Austria.[1] It was patented in 1909.[2]

Category

Sulfonamide

US Brand Names

AVC VAGINAL®

FDA Package Insert

Description | Clinical Pharmacology | Microbiology | Indications and Usage | Contraindications | Warnings and Precautions | Adverse Reactions | Overdosage | Dosage and Administration | How Supplied | Labels and Packages

Mechanism of Action

As a sulfonamide antibiotic, it functions by competitively inhibiting (i.e., by acting as a substrate analogue) enzymatic reactions involving para-aminobenzoic acid (PABA).[3] PABA is needed in enzymatic reactions that produce folic acid which acts as a coenzyme in the synthesis of purine, pyrimidine and other amino acids.

References

  1. Paul Gelmo (May 14, 1908) "Über Sulfamide der p-Amidobenzolsulfonsäure," Journal für Praktische Chemie, 77 : 369-382.
  2. On May 18, 1909, Deutsches Reich Patentschrift number 226,239 for sulfanilamide was awarded to Heinrich Hörlein of the Bayer corporation.
  3. Michael Kent, Advanced Biology, Oxford University Press, 2000, p. 46 ISBN 978-0-19-914195-1