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Sulfathiazole

Catalog No. Bio-0804 Name InterBioScreen
CAS Number 72-14-0 Website http://www.ibscreen.com
M. F. C9H9N3O2S2 Telephone +7 49652 40091
M. W. 255.31666 Fax
Purity Email screen@ibscreen.chg.ru
Storage Chembase ID: 4415

SYNONYMS

IUPAC name
4-amino-N-(1,3-thiazol-2-yl)benzene-1-sulfonamide
IUPAC Traditional name
4-amino-N-(1,3-thiazol-2-yl)benzene-1-sulfonamide
Synonyms
Sultrin

DATABASE IDS

CAS Number 72-14-0

PROPERTIES

Application(s) Sulfonamide
Application(s) Used in treatment of severe staphylococcal infections, but use restricted due to its systemic toxicity.
Mechanism of Action Dihydrofolate reductase inhibitor
Mechanism of Action Dihydrofolate synthesis inhibitor
Mechanism of Action Folate-antagonist

DETAILS

REFERENCES

  • Fosbinder, R.J., J.A.C.S., 1939, 61, 2032, (synth)
  • Capitan, F. et al., Inf. Quim. Anal., 1970, 24, 100, (use)
  • Bass, A.D. et al., Drill's Pharmacol. Med., 4th edn., McGraw-Hill, New York, 1971, 1657, (pharmacol)
  • Kracmar, J. et al., Pharmazie, 1975, 30, 447, (uv)
  • Forlani, L., Gazz. Chim. Ital., 1981, 111, 159, (pmr, tautom)
  • Haley, T.J., Dangerous Prop. Ind. Mater. Rep., 1983, 3, 9, (rev, pharmacol, tox)
  • Bult, A., Pharm. Weekbl., Sci. Ed., 1983, 5, 77, (cmr, tautom)
  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th edn., Akademie-Verlag, 1987, 1148
  • Kirk-Othmer Encycl. Chem. Technol., 4th edn., Wiley, 1991, 2, 876, (rev)
  • Kapoor, V.K., Anal. Profiles Drug Subst., 1993, 22, 389, (rev)
  • Martindale, The Extra Pharmacopoeia, 30th edn., Pharmaceutical Press, 1993, 210
  • Hughes, D.S. et al., Acta Cryst. C, 1999, 55, 1831-1833, (cryst struct)
  • Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, TEX250; TEX500