Bisphosphonates derived from fatty acids are potent inhibitors of Trypanosoma cruzi farnesyl pyrophosphate synthase

Studies on the mode of action of a series of bisphosphonates derived from fatty acids, which had previously proved to be potent inhibitors against Trypanosoma cruzi proliferation in in vitro assays, have been performed. Some of these drugs proved to be potent inhibitors against the intracellular for...

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Autores principales: Szajnman, Sergio Hernán, Rodríguez, Juan Bautista
Publicado: 2003
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0960894X_v13_n19_p3231_Szajnman
http://hdl.handle.net/20.500.12110/paper_0960894X_v13_n19_p3231_Szajnman
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spelling paper:paper_0960894X_v13_n19_p3231_Szajnman2023-06-08T15:57:49Z Bisphosphonates derived from fatty acids are potent inhibitors of Trypanosoma cruzi farnesyl pyrophosphate synthase Szajnman, Sergio Hernán Rodríguez, Juan Bautista fatty acid derivative geranyltransferase phosphonic acid derivative anorexia article cell proliferation drug approval drug potency food and drug administration IC 50 in vitro study inhibition kinetics nonhuman osteolysis parasite peripheral neuropathy skin allergy tropical disease Trypanosoma cruzi vomiting Trypanosoma Trypanosoma cruzi Studies on the mode of action of a series of bisphosphonates derived from fatty acids, which had previously proved to be potent inhibitors against Trypanosoma cruzi proliferation in in vitro assays, have been performed. Some of these drugs proved to be potent inhibitors against the intracellular form of the parasite, exhibiting IC50 values at the low micromolar level. As bisphosphonates are FDA clinically approved for treatment of bone resorption disorders, their potential innocuousness makes them good candidates to control tropical diseases. © 2003 Elsevier Ltd. All rights reserved. Fil:Szajnman, S.H. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Rodriguez, J.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2003 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0960894X_v13_n19_p3231_Szajnman http://hdl.handle.net/20.500.12110/paper_0960894X_v13_n19_p3231_Szajnman
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic fatty acid derivative
geranyltransferase
phosphonic acid derivative
anorexia
article
cell proliferation
drug approval
drug potency
food and drug administration
IC 50
in vitro study
inhibition kinetics
nonhuman
osteolysis
parasite
peripheral neuropathy
skin allergy
tropical disease
Trypanosoma cruzi
vomiting
Trypanosoma
Trypanosoma cruzi
spellingShingle fatty acid derivative
geranyltransferase
phosphonic acid derivative
anorexia
article
cell proliferation
drug approval
drug potency
food and drug administration
IC 50
in vitro study
inhibition kinetics
nonhuman
osteolysis
parasite
peripheral neuropathy
skin allergy
tropical disease
Trypanosoma cruzi
vomiting
Trypanosoma
Trypanosoma cruzi
Szajnman, Sergio Hernán
Rodríguez, Juan Bautista
Bisphosphonates derived from fatty acids are potent inhibitors of Trypanosoma cruzi farnesyl pyrophosphate synthase
topic_facet fatty acid derivative
geranyltransferase
phosphonic acid derivative
anorexia
article
cell proliferation
drug approval
drug potency
food and drug administration
IC 50
in vitro study
inhibition kinetics
nonhuman
osteolysis
parasite
peripheral neuropathy
skin allergy
tropical disease
Trypanosoma cruzi
vomiting
Trypanosoma
Trypanosoma cruzi
description Studies on the mode of action of a series of bisphosphonates derived from fatty acids, which had previously proved to be potent inhibitors against Trypanosoma cruzi proliferation in in vitro assays, have been performed. Some of these drugs proved to be potent inhibitors against the intracellular form of the parasite, exhibiting IC50 values at the low micromolar level. As bisphosphonates are FDA clinically approved for treatment of bone resorption disorders, their potential innocuousness makes them good candidates to control tropical diseases. © 2003 Elsevier Ltd. All rights reserved.
author Szajnman, Sergio Hernán
Rodríguez, Juan Bautista
author_facet Szajnman, Sergio Hernán
Rodríguez, Juan Bautista
author_sort Szajnman, Sergio Hernán
title Bisphosphonates derived from fatty acids are potent inhibitors of Trypanosoma cruzi farnesyl pyrophosphate synthase
title_short Bisphosphonates derived from fatty acids are potent inhibitors of Trypanosoma cruzi farnesyl pyrophosphate synthase
title_full Bisphosphonates derived from fatty acids are potent inhibitors of Trypanosoma cruzi farnesyl pyrophosphate synthase
title_fullStr Bisphosphonates derived from fatty acids are potent inhibitors of Trypanosoma cruzi farnesyl pyrophosphate synthase
title_full_unstemmed Bisphosphonates derived from fatty acids are potent inhibitors of Trypanosoma cruzi farnesyl pyrophosphate synthase
title_sort bisphosphonates derived from fatty acids are potent inhibitors of trypanosoma cruzi farnesyl pyrophosphate synthase
publishDate 2003
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0960894X_v13_n19_p3231_Szajnman
http://hdl.handle.net/20.500.12110/paper_0960894X_v13_n19_p3231_Szajnman
work_keys_str_mv AT szajnmansergiohernan bisphosphonatesderivedfromfattyacidsarepotentinhibitorsoftrypanosomacruzifarnesylpyrophosphatesynthase
AT rodriguezjuanbautista bisphosphonatesderivedfromfattyacidsarepotentinhibitorsoftrypanosomacruzifarnesylpyrophosphatesynthase
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