
Bioorganic and Medicinal Chemistry Letters p. 3621 - 3626 (1998)
Update date:2022-08-29
Topics:
Nadler, Guy
Morvan, Marcel
Delimoge, Isabelle
Belfiore, Pietro
Zocchetti, Andrea
James, Ian
Zembryki, Denise
Lee-Rycakzewski, Elizabeth
Parini, Carlo
Consolandi, Emanuela
Gagliardi, Stefania
Farina, Carlo
Optimisation of a novel series of osteoclast ATPase inhibitors led to (2Z,4E)-5-(5,6-dichloro-2-indolyl)-2-methoxy-N-(1,2,2,6,6- pentamethylpiperidin-4-yl)-2,4-pentadienamide (1) that was the most potent compound in an in vitro osteoclast ATPase assay and in human bone resorption assays. Two of the possible geometric isomers have also been prepared and shown to be significantly less potent than 1.
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