cAMP analogs and selective inhibitors used to study low Km Mucor rouxii cAMP phosphodiesterase

Autores
Tomes, C.; Moreno, S.
Año de publicación
1990
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
1. 1. The sensitivity of partially purified low Km, phosphodiesterase (PDE) from Mucor rouxii to pharmacological agents and cAMP analogs was studied. The IC50 obtained were compared with those reported for PDEs from higher eukaryotes. 2. 2. The best inhibitors of the hydrolysis of 1 gmM cAMP were SQ 65.442 (IC50, c 10 μM), dipyridamol and CI 930. cGMP was not an inhibitor (IC50 > 1000 μm). 3. 3. The cAMP analogs were tested as inhibitors of the hydrolysis of 0. l μM cAMP. 8-Aminohexylamino cAMP was the best inhibitor with an IC50 of c 1 μM. 4. 4. A sedimentation profile of Mucor PDE was assayed in the presence of several pharmacological inhibitors and eAMP analogs. No isoforms with different sensitivity towards the inhibitors were detected. Forms with slightly different behaviour towards some cAMP analogs were observed. © 1990.
Fil:Tomes, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Moreno, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fuente
Int. J. Biochem. 1990;22(9):1047-1051
Materia
1 ethyl 4 hydrazino 1h pyrazolo[3,4 b]pyridine 5 carboxylic acid ethyl ester
4 (3 butoxy 4 methoxybenzyl) 2 imidazolidinone
4,5 dihydro 6 [4 (1h imidazol 1 yl)phenyl] 5 methyl 3(2h) pyridazinone
6 [4 (3 methylureido)phenyl] 3(2h) pyridazinone
amrinone
cilostamide
cilostazol
cyclic amp
dipyridamole
etazolate
imazodan
isobutylmethylxanthine
milrinone
papaverine
phosphodiesterase
phosphodiesterase inhibitor
rolipram
sq 65442
theophylline
unclassified drug
article
fungus
mucor
nonhuman
1-Methyl-3-isobutylxanthine
3',5'-Cyclic-Nucleotide Phosphodiesterase
Centrifugation, Density Gradient
Cyclic AMP
Cyclic GMP
Dipyridamole
Hydrolysis
Mucor
Nicotinic Acids
Papaverine
Pyridazines
Support, Non-U.S. Gov't
Theophylline
Amylomyces rouxii
Fungi
Mucor
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/2.5/ar
Repositorio
Biblioteca Digital (UBA-FCEN)
Institución
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
OAI Identificador
paperaa:paper_0020711X_v22_n9_p1047_Tomes

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oai_identifier_str paperaa:paper_0020711X_v22_n9_p1047_Tomes
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling cAMP analogs and selective inhibitors used to study low Km Mucor rouxii cAMP phosphodiesteraseTomes, C.Moreno, S.1 ethyl 4 hydrazino 1h pyrazolo[3,4 b]pyridine 5 carboxylic acid ethyl ester4 (3 butoxy 4 methoxybenzyl) 2 imidazolidinone4,5 dihydro 6 [4 (1h imidazol 1 yl)phenyl] 5 methyl 3(2h) pyridazinone6 [4 (3 methylureido)phenyl] 3(2h) pyridazinoneamrinonecilostamidecilostazolcyclic ampdipyridamoleetazolateimazodanisobutylmethylxanthinemilrinonepapaverinephosphodiesterasephosphodiesterase inhibitorrolipramsq 65442theophyllineunclassified drugarticlefungusmucornonhuman1-Methyl-3-isobutylxanthine3',5'-Cyclic-Nucleotide PhosphodiesteraseCentrifugation, Density GradientCyclic AMPCyclic GMPDipyridamoleHydrolysisMucorNicotinic AcidsPapaverinePyridazinesSupport, Non-U.S. Gov'tTheophyllineAmylomyces rouxiiFungiMucor1. 1. The sensitivity of partially purified low Km, phosphodiesterase (PDE) from Mucor rouxii to pharmacological agents and cAMP analogs was studied. The IC50 obtained were compared with those reported for PDEs from higher eukaryotes. 2. 2. The best inhibitors of the hydrolysis of 1 gmM cAMP were SQ 65.442 (IC50, c 10 μM), dipyridamol and CI 930. cGMP was not an inhibitor (IC50 > 1000 μm). 3. 3. The cAMP analogs were tested as inhibitors of the hydrolysis of 0. l μM cAMP. 8-Aminohexylamino cAMP was the best inhibitor with an IC50 of c 1 μM. 4. 4. A sedimentation profile of Mucor PDE was assayed in the presence of several pharmacological inhibitors and eAMP analogs. No isoforms with different sensitivity towards the inhibitors were detected. Forms with slightly different behaviour towards some cAMP analogs were observed. © 1990.Fil:Tomes, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Moreno, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.1990info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_0020711X_v22_n9_p1047_TomesInt. J. Biochem. 1990;22(9):1047-1051reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2025-10-16T09:30:10Zpaperaa:paper_0020711X_v22_n9_p1047_TomesInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-10-16 09:30:12.002Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv cAMP analogs and selective inhibitors used to study low Km Mucor rouxii cAMP phosphodiesterase
title cAMP analogs and selective inhibitors used to study low Km Mucor rouxii cAMP phosphodiesterase
spellingShingle cAMP analogs and selective inhibitors used to study low Km Mucor rouxii cAMP phosphodiesterase
Tomes, C.
1 ethyl 4 hydrazino 1h pyrazolo[3,4 b]pyridine 5 carboxylic acid ethyl ester
4 (3 butoxy 4 methoxybenzyl) 2 imidazolidinone
4,5 dihydro 6 [4 (1h imidazol 1 yl)phenyl] 5 methyl 3(2h) pyridazinone
6 [4 (3 methylureido)phenyl] 3(2h) pyridazinone
amrinone
cilostamide
cilostazol
cyclic amp
dipyridamole
etazolate
imazodan
isobutylmethylxanthine
milrinone
papaverine
phosphodiesterase
phosphodiesterase inhibitor
rolipram
sq 65442
theophylline
unclassified drug
article
fungus
mucor
nonhuman
1-Methyl-3-isobutylxanthine
3',5'-Cyclic-Nucleotide Phosphodiesterase
Centrifugation, Density Gradient
Cyclic AMP
Cyclic GMP
Dipyridamole
Hydrolysis
Mucor
Nicotinic Acids
Papaverine
Pyridazines
Support, Non-U.S. Gov't
Theophylline
Amylomyces rouxii
Fungi
Mucor
title_short cAMP analogs and selective inhibitors used to study low Km Mucor rouxii cAMP phosphodiesterase
title_full cAMP analogs and selective inhibitors used to study low Km Mucor rouxii cAMP phosphodiesterase
title_fullStr cAMP analogs and selective inhibitors used to study low Km Mucor rouxii cAMP phosphodiesterase
title_full_unstemmed cAMP analogs and selective inhibitors used to study low Km Mucor rouxii cAMP phosphodiesterase
title_sort cAMP analogs and selective inhibitors used to study low Km Mucor rouxii cAMP phosphodiesterase
dc.creator.none.fl_str_mv Tomes, C.
Moreno, S.
author Tomes, C.
author_facet Tomes, C.
Moreno, S.
author_role author
author2 Moreno, S.
author2_role author
dc.subject.none.fl_str_mv 1 ethyl 4 hydrazino 1h pyrazolo[3,4 b]pyridine 5 carboxylic acid ethyl ester
4 (3 butoxy 4 methoxybenzyl) 2 imidazolidinone
4,5 dihydro 6 [4 (1h imidazol 1 yl)phenyl] 5 methyl 3(2h) pyridazinone
6 [4 (3 methylureido)phenyl] 3(2h) pyridazinone
amrinone
cilostamide
cilostazol
cyclic amp
dipyridamole
etazolate
imazodan
isobutylmethylxanthine
milrinone
papaverine
phosphodiesterase
phosphodiesterase inhibitor
rolipram
sq 65442
theophylline
unclassified drug
article
fungus
mucor
nonhuman
1-Methyl-3-isobutylxanthine
3',5'-Cyclic-Nucleotide Phosphodiesterase
Centrifugation, Density Gradient
Cyclic AMP
Cyclic GMP
Dipyridamole
Hydrolysis
Mucor
Nicotinic Acids
Papaverine
Pyridazines
Support, Non-U.S. Gov't
Theophylline
Amylomyces rouxii
Fungi
Mucor
topic 1 ethyl 4 hydrazino 1h pyrazolo[3,4 b]pyridine 5 carboxylic acid ethyl ester
4 (3 butoxy 4 methoxybenzyl) 2 imidazolidinone
4,5 dihydro 6 [4 (1h imidazol 1 yl)phenyl] 5 methyl 3(2h) pyridazinone
6 [4 (3 methylureido)phenyl] 3(2h) pyridazinone
amrinone
cilostamide
cilostazol
cyclic amp
dipyridamole
etazolate
imazodan
isobutylmethylxanthine
milrinone
papaverine
phosphodiesterase
phosphodiesterase inhibitor
rolipram
sq 65442
theophylline
unclassified drug
article
fungus
mucor
nonhuman
1-Methyl-3-isobutylxanthine
3',5'-Cyclic-Nucleotide Phosphodiesterase
Centrifugation, Density Gradient
Cyclic AMP
Cyclic GMP
Dipyridamole
Hydrolysis
Mucor
Nicotinic Acids
Papaverine
Pyridazines
Support, Non-U.S. Gov't
Theophylline
Amylomyces rouxii
Fungi
Mucor
dc.description.none.fl_txt_mv 1. 1. The sensitivity of partially purified low Km, phosphodiesterase (PDE) from Mucor rouxii to pharmacological agents and cAMP analogs was studied. The IC50 obtained were compared with those reported for PDEs from higher eukaryotes. 2. 2. The best inhibitors of the hydrolysis of 1 gmM cAMP were SQ 65.442 (IC50, c 10 μM), dipyridamol and CI 930. cGMP was not an inhibitor (IC50 > 1000 μm). 3. 3. The cAMP analogs were tested as inhibitors of the hydrolysis of 0. l μM cAMP. 8-Aminohexylamino cAMP was the best inhibitor with an IC50 of c 1 μM. 4. 4. A sedimentation profile of Mucor PDE was assayed in the presence of several pharmacological inhibitors and eAMP analogs. No isoforms with different sensitivity towards the inhibitors were detected. Forms with slightly different behaviour towards some cAMP analogs were observed. © 1990.
Fil:Tomes, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Moreno, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
description 1. 1. The sensitivity of partially purified low Km, phosphodiesterase (PDE) from Mucor rouxii to pharmacological agents and cAMP analogs was studied. The IC50 obtained were compared with those reported for PDEs from higher eukaryotes. 2. 2. The best inhibitors of the hydrolysis of 1 gmM cAMP were SQ 65.442 (IC50, c 10 μM), dipyridamol and CI 930. cGMP was not an inhibitor (IC50 > 1000 μm). 3. 3. The cAMP analogs were tested as inhibitors of the hydrolysis of 0. l μM cAMP. 8-Aminohexylamino cAMP was the best inhibitor with an IC50 of c 1 μM. 4. 4. A sedimentation profile of Mucor PDE was assayed in the presence of several pharmacological inhibitors and eAMP analogs. No isoforms with different sensitivity towards the inhibitors were detected. Forms with slightly different behaviour towards some cAMP analogs were observed. © 1990.
publishDate 1990
dc.date.none.fl_str_mv 1990
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/20.500.12110/paper_0020711X_v22_n9_p1047_Tomes
url http://hdl.handle.net/20.500.12110/paper_0020711X_v22_n9_p1047_Tomes
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/2.5/ar
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/ar
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Int. J. Biochem. 1990;22(9):1047-1051
reponame:Biblioteca Digital (UBA-FCEN)
instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
reponame_str Biblioteca Digital (UBA-FCEN)
collection Biblioteca Digital (UBA-FCEN)
instname_str Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron_str UBA-FCEN
institution UBA-FCEN
repository.name.fl_str_mv Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
repository.mail.fl_str_mv ana@bl.fcen.uba.ar
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