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Synthesis and cytotoxic activity of a new series of topoisomerase I inhibitors.
Bioorg Med Chem Lett. 2008 Feb 15;18(4):1484-9. doi: 10.1016/j.bmcl.2007.12.055. Epub 2007 Dec 25.
Bioorg Med Chem Lett. 2008.
PMID: 18248813
Interaction between double helix DNA fragments and a new topopyrone acting as human topoisomerase I poison.
Scaglioni L, Mazzini S, Mondelli R, Dallavalle S, Gattinoni S, Tinelli S, Beretta GL, Zunino F, Ragg E.
Scaglioni L, et al. Among authors: gattinoni s.
Bioorg Med Chem. 2009 Jan 15;17(2):484-91. doi: 10.1016/j.bmc.2008.12.005. Epub 2008 Dec 10.
Bioorg Med Chem. 2009.
PMID: 19097800
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A new group of oxime carbamates as reversible inhibitors of fatty acid amide hydrolase.
Gattinoni S, Simone CD, Dallavalle S, Fezza F, Nannei R, Battista N, Minetti P, Quattrociocchi G, Caprioli A, Borsini F, Cabri W, Penco S, Merlini L, Maccarrone M.
Gattinoni S, et al.
Bioorg Med Chem Lett. 2010 Aug 1;20(15):4406-11. doi: 10.1016/j.bmcl.2010.06.050. Epub 2010 Jun 15.
Bioorg Med Chem Lett. 2010.
PMID: 20591666
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Enol carbamates as inhibitors of fatty acid amide hydrolase (FAAH) endowed with high selectivity for FAAH over the other targets of the endocannabinoid system.
Gattinoni S, De Simone C, Dallavalle S, Fezza F, Nannei R, Amadio D, Minetti P, Quattrociocchi G, Caprioli A, Borsini F, Cabri W, Penco S, Merlini L, Maccarrone M.
Gattinoni S, et al.
ChemMedChem. 2010 Mar 1;5(3):357-60. doi: 10.1002/cmdc.200900472.
ChemMedChem. 2010.
PMID: 20112328
No abstract available.
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