Substituted 9-aminoacridine-4-carboxamides tethered to platinum(II)diamine complexes: Chemistry, cytotoxicity and DNA sequence selectivity

Carland, Michael W.; Grannas, Martin J.; Cairns, Murray J.; Roknic, Vanessa J.; Denny, William A.; McFadyen, W. David; Murray, Vincent

doi:10.1016/j.jinorgbio.2010.03.011

Cited by 12 publications

(2 citation statements)

References 30 publications

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“…9,10-Dioxoanthracene-1,4-diyl bis(4-methylbenzenesulfonate) Thapong Teerawatananond, Chiaranan Kerdsamut, Sirirat Kokpol and Nongnuj Muangsin Comment Anthraquinone and its derivatives have been studies in the many fields, for example, antimicrobial and antibiotic activity (García-Sosa et al, 2006), anticancer agents (Huang, et al, 2004;Carland et al, 2010). Additionally, both of unsubstituted and substituted anthraquinone play an important role in various photochemical and colorimetric sensor systems (Cho et al, 2006).…”

Section: Methodsmentioning

confidence: 99%

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9,10-Dioxoanthracene-1,4-diyl bis(4-methylbenzenesulfonate)

Teerawatananond¹,

Kerdsamut²,

Kokpol³

et al. 2012

Acta Cryst E

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The title molecule, C28H20O8S2, has a T-shaped conformation. The central 9,10-anthraquinone moiety is bow-shaped with the two outer aromatic rings being inclined to one another by 13.99 (11)°. The benzenesulfonate rings are inclined to one another by 47.35 (12)°, and by 34.51 (11) and 17.88 (11)° to the bridging aromatic ring of the 9,10-anthraquinone moiety. In the crystal, C—H⋯O interactions link the molecules into ribbons in [100].

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Section: Methodsmentioning

confidence: 99%

“…For background to the structures of anthraquinones and their biological activity, see: Zielske (1987); Yatsenko et al (2000); Huang et al (2004); Meng et al (2005); García-Sosa et al (2006); Cho et al (2006); Carland et al (2010). For related structures, see: Swaminathan & Nigam (1967); Cao et al (2007).…”

Section: Related Literaturementioning

confidence: 99%