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Synthesis of isoprenoid bisphosphonate ethers through C-P bond formations: Potential inhibitors of geranylgeranyl diphosphate synthase.

Authors :
Zhou X
Reilly JE
Loerch KA
Hohl RJ
Wiemer DF
Source :
Beilstein journal of organic chemistry [Beilstein J Org Chem] 2014 Jul 18; Vol. 10, pp. 1645-50. Date of Electronic Publication: 2014 Jul 18 (Print Publication: 2014).
Publication Year :
2014

Abstract

A set of bisphosphonate ethers has been prepared through sequential phosphonylation and alkylation of monophosphonate ethers. After formation of the corresponding phosphonic acid salts, these compounds were tested for their ability to inhibit the enzyme geranylgeranyl diphosphate synthase (GGDPS). Five of the new compounds show IC50 values of less than 1 μM against GGDPS with little to no activity against the related enzyme farnesyl diphosphate synthase (FDPS). The most active compound displayed an IC50 value of 82 nM when assayed with GGDPS, and no activity against FDPS even at a 10 μM concentration.

Details

Language :
English
ISSN :
1860-5397
Volume :
10
Database :
MEDLINE
Journal :
Beilstein journal of organic chemistry
Publication Type :
Academic Journal
Accession number :
25161722
Full Text :
https://doi.org/10.3762/bjoc.10.171