کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1356329 | 1500470 | 2012 | 7 صفحه PDF | دانلود رایگان |
A series 6-aryl-pyrrolo[2,3-d]pyrimidine-4-amines (43 compounds), some of which are epidermal growth factor tyrosine kinase inhibitors, were tested for their protozoal toxicity using an environmental Tetrahymena strain as model organism. The protozoacidal activity of the analogues was found to be highly dependent on a 4-hydroxyl group at the 6-aryl ring, and a chiral 1-phenylethanamine substituent in position 4. Further, the potency was affected by the aromatic substitution pattern of the phenylethanamine: the unsubstituted, the meta-fluoro and the para-bromo substituted derivatives had the lowest minimum protozoacidal concentrations (8–16 μg/mL). Surprisingly, both enantiomers were found to have high potency suggesting that this compound class could have several modes of action. No correlation was found between the compounds protozoacidal activity and the in vitro epidermal growth factor receptor tyrosine kinase inhibitory potency. This suggests that the observed antimicrobial effects are related to other targets. Testing towards a panel of kinases indicated several alternative modes of action.
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► 6-Aryl-pyrrolopyrimidine-4-amines were tested for their antiprotozoal effect.
► Tetrahymena was used as model organism.
► The most active compounds had an MPC-values of 8–16 μg/mL.
► Structural units needed for antiprotozoal activity were identified.
► Testing towards a panel of kinases indicate several possible targets and putative mechanisms.
Journal: Bioorganic Chemistry - Volume 44, October 2012, Pages 35–41