| Literature DB >> 9934482 |
G Nadler1, M Morvan, I Delimoge, P Belfiore, A Zocchetti, I James, D Zembryki, E Lee-Rycakzewski, C Parini, E Consolandi, S Gagliardi, C Farina.
Abstract
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.Entities:
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Year: 1998 PMID: 9934482 DOI: 10.1016/s0960-894x(98)00660-x
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823