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
- Institución
- Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
- OAI Identificador
- paperaa:paper_0020711X_v22_n9_p1047_Tomes
Ver los metadatos del registro completo
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paperaa:paper_0020711X_v22_n9_p1047_Tomes |
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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 |
_version_ |
1846142847287296000 |
score |
12.712165 |