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1-(Fluoroalkylidene)-1,1-bisphosphonic acids are potent and selective inhibitors of the enzymatic activity of Toxoplasma gondii farnesyl pyrophosphate synthase.

Abstract
α-Fluorinated-1,1-bisphosphonic acids derived from fatty acids were designed, synthesized and biologically evaluated against Trypanosoma cruzi, the etiologic agent of Chagas disease, and against Toxoplasma gondii, the agent responsible for toxoplasmosis, and also towards the target parasitic enzymes farnesyl pyrophosphate synthase of T. cruzi (TcFPPS) and T. gondii (TgFPPS). Interestingly, 1-fluorononylidene-1,1-bisphosphonic acid (compound 43) proved to be an extremely potent inhibitor of the enzymatic activity of TgFPPS at the low nanomolar range, exhibiting an IC(50) of 30 nM. This compound was two-fold more potent than risedronate (IC(50) = 74 nM) that was taken as a positive control. This enzymatic activity was associated with a strong cell growth inhibition against tachyzoites of T. gondii, with an IC(50) value of 2.7 μM.
AuthorsSergio H Szajnman, Valeria S Rosso, Leena Malayil, Alyssa Smith, Silvia N J Moreno, Roberto Docampo, Juan B Rodriguez
JournalOrganic & biomolecular chemistry (Org Biomol Chem) Vol. 10 Issue 7 Pg. 1424-33 (Feb 21 2012) ISSN: 1477-0539 [Electronic] England
PMID22215028 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • 1-fluorononylidene-1,1-bisphosphonic acid
  • Antiprotozoal Agents
  • Diphosphonates
  • Enzyme Inhibitors
  • Geranyltranstransferase
Topics
  • Antiprotozoal Agents (chemistry, pharmacology)
  • Diphosphonates (chemistry, pharmacology)
  • Enzyme Inhibitors (chemistry, pharmacology)
  • Geranyltranstransferase (antagonists & inhibitors, metabolism)
  • Toxoplasma (enzymology, metabolism)

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