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Solasulfone

From Wikipedia, the free encyclopedia
Solasulfone
Names
IUPAC name
Tetrasodium 3,3'-[sulfonylbis(benzene-4,1-diylimino)]bis(1-phenylpropane-1,3-disulfonate)
Other names
Solapsone; Sulfetrone
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.004.652Edit this at Wikidata
UNII
  • InChI=1S/C30H32N2O14S5.4Na/c33-47(34,25-15-11-23(12-16-25)31-29(50(41,42)43)19-27(48(35,36)37)21-7-3-1-4-8-21)26-17-13-24(14-18-26)32-30(51(44,45)46)20-28(49(38,39)40)22-9-5-2-6-10-22;;;;/h1-18,27-32H,19-20H2,(H,35,36,37)(H,38,39,40)(H,41,42,43)(H,44,45,46);;;;/q;4*+1/p-4
  • [Na+].[Na+].[Na+].[Na+].[O-]S(=O)(=O)C(c1ccccc1)CC(Nc2ccc(cc2)S(=O)(=O)c4ccc(NC(S([O-])(=O)=O)CC(c3ccccc3)S([O-])(=O)=O)cc4)S([O-])(=O)=O
Properties
C30H28N2Na4O14S5
Molar mass 892.81g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state(at 25 °C [77 °F], 100 kPa).

Solasulfoneis anantileprotic drugdeveloped from the parent compound sulphetrone.[1]It was first described and evaluated in the 1930s and 1940s as an antibacterial agent for the treatment oftuberculosisand various other infections, and later found to be effective in the treatment ofleprosy.[2]

References

[edit]
  1. ^Chemistry for Pharmacy and the Life Sciences(1996, Pearson Education Limited) Thomas, Gareth; ppg. 349-350
  2. ^Brownlee, George; Green, A. F.; Woodbine, M. (March 1948)."Sulphetrone*: A Chemotherapeutic Agent for Tuberculosis: Pharmacology and Chemotherapy".British Journal of Pharmacology and Chemotherapy.3(1): 15–28.doi:10.1111/j.1476-5381.1948.tb00348.x.PMC1509804.PMID18904720.