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. 2019 Jan 29;54(4):1256–1270. doi: 10.3892/ijo.2019.4701

Table I.

List of compounds.

Common name, synonym Chemical, formal name Laboratory number IC50 (mM) Source
Salicylic acid, SA 2-hydroxybenzoic acid Not applicable 2.6 Commercially available
Aspirin, ortho-aspirin 2-acetoxybenzoic acid, acetylsalicylic acid PN502 1.8 Commercially available
Diaspirin, DiA Bis-carboxyphenylsuccinate PN508 0.8 (27)
Fumaryldiaspirin, F-DiA Bis-carboxyphenylfumarate PN517 0.2 (27)
Not applicable m-bromobenzoylsalicylic acid PN524 0.4 (27)
Not applicable Isopropyl m-bromobenzoylsalicylate PN529 ND (27)
meta-aspirin 3-acetoxybenzoic acid PN548 3.8 Synthesised in this study
para-aspirin 4-acetoxybenzoic acid PN549 4.9 Synthesised in this study
Thioaspirin, ortho-TASP 2-acetylthiobenzoic acid PN590 0.2 Synthesised in this study
m-thioaspirin, meta-TASP 3-acetylthiobenzoic acid PN591 0.5 Synthesised in this study
p-thioaspirin, para-TASP 4-acetylthiobenzoic acid PN592 0.8 Synthesised in this study
Diflunisal, DIF 5-(2,4-difluorophenyl) salicylic acid Not applicable 0.08 Commercially available

IC50, half maximal inhibitory concentration; ND, not determined.