| Literature DB >> 10896113 |
G H Posner1, J P Maxwell, H O'Dowd, M Krasavin, S Xie, T A Shapiro.
Abstract
A series of trioxanes featuring sulfide, sulfone, and sulfonamide substituents in diverse positions has been prepared. Structure-activity relationship (SAR) generalizations highlight two major factors controlling the antimalarial potency of these new chemical entities: (1) the proximity of the sulfur-containing substituent to the crucial peroxide bond and (2) the oxidation state of the sulfur-containing substituent. Generally, sulfones are more antimalarially potent than the corresponding sulfides.Entities:
Mesh:
Substances:
Year: 2000 PMID: 10896113 DOI: 10.1016/s0968-0896(00)00079-1
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641