Journal of Medicinal Chemistry · 2005 · 474 citations · 18 references
MedicineMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryMolecular PharmacologyOncology PharmacologyPharmacodynamics Of Anticancer AgentsAntiproliferative AgentsAntiproliferative Drug ActionBenzothiazole SynthesisCancer Cell Line ModelsChemical Structure-activity RelationshipsThiazole Chemistry
A series of new 2-phenylbenzothiazoles has been synthesized on the basis of the discovery of the potent and selective in vitro antitumor properties of 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (8n; GW 610, NSC 721648). Synthesis of analogues substituted in the benzothiazole ring was achieved via the reaction of o-aminothiophenol disulfides with substituted benzaldehydes under reducing conditions. Compounds were evaluated in vitro in four human cancer cell lines, and compound 8n was found to possess exquisitely potent antiproliferative activity (GI(50) < 0.1 nM for MCF-7 and MDA 468). Potent and selective activity was also observed in the NCI 60 human cancer cell line panel. Structure-activity relationships established that the compound 8n stands on a pinnacle of potent activity, with most structural variations having a deactivating in vitro effect. Mechanistically, this new series of agents contrasts with the previously reported 2-(4-aminophenyl)benzothiazoles; compound 8n is not reliant on induction of CYP1A1 expression for antitumor activity.
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Dong‐Fang Shi, Tracey D. Bradshaw, Samantha Wrigley et al. · Journal of Medicinal Chemistry · 1996 · 369 citations