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pubmed-article:18642893pubmed:abstractTextA new inhibitor for human sirtuin type proteins 1 and 2 (SIRT1 and SIRT2) was discovered through virtual database screening in search of new scaffolds. A series of compounds was synthesized based on the hit compound (3-[[3-(4-tert-butylphenyl)1,2,4-oxadiazole-5-carbonyl]amino]-1-[3-(trifluoromethyl)phenyl]thiourea). The most potent compound in the series was nearly as potent as the reference compound (6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide).lld:pubmed
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pubmed-article:18642893pubmed:articleTitleOxadiazole-carbonylaminothioureas as SIRT1 and SIRT2 inhibitors.lld:pubmed
pubmed-article:18642893pubmed:affiliationDepartment of Pharmaceutical Chemistry, University of Kuopio, PO Box 1627, 70211 Kuopio, Finland. tero.huhtiniemi@uku.filld:pubmed
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