Induction of quinone reductase by withanolides

Thirty-seven naturally occurring withanolides (1-37), previously isolated in our laboratories, were evaluated for their potential to induce quinone reductase with cultured murine hepatoma cells (Hepa 1c1c7). Spiranoid (29, 32) and 18-functionalized withanolides (2-5, 7-9, 24) were found to be potent...

Descripción completa

Detalles Bibliográficos
Autores principales: Veleiro, Adriana Silvia, Cirigliano, Adriana Mónica, Tettamanzi, María Cristina, Burton, Gerardo
Publicado: 2002
Materias:
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01633864_v65_n5_p677_Misico
http://hdl.handle.net/20.500.12110/paper_01633864_v65_n5_p677_Misico
Aporte de:
id paper:paper_01633864_v65_n5_p677_Misico
record_format dspace
spelling paper:paper_01633864_v65_n5_p677_Misico2023-06-08T15:14:15Z Induction of quinone reductase by withanolides Veleiro, Adriana Silvia Cirigliano, Adriana Mónica Tettamanzi, María Cristina Burton, Gerardo 18 hydroxywithanolide d enzyme inducing agent jaborosalactone 1 joborosalactone p reduced nicotinamide adenine dinucleotide (phosphate) dehydrogenase (quinone) unclassified drug withanolide derivative withaphysalin g withaphysalin h withaphysalin i withaphysalin j animal cell animal experiment animal tissue article breast colon concentration response controlled study drug potency drug structure enzyme induction hepatoma cell liver lung mouse nonhuman phytochemistry stomach Animals Brassicaceae Breast Carcinoma, Hepatocellular Colon Enzyme Induction Inhibitory Concentration 50 Liver Lung Mice Mice, Inbred BALB C Molecular Structure Nuclear Magnetic Resonance, Biomolecular Plants, Medicinal Quinone Reductases Solanaceae Stereoisomerism Steroids Stilbenes Stomach Tumor Cells, Cultured Animalia Murinae Thirty-seven naturally occurring withanolides (1-37), previously isolated in our laboratories, were evaluated for their potential to induce quinone reductase with cultured murine hepatoma cells (Hepa 1c1c7). Spiranoid (29, 32) and 18-functionalized withanolides (2-5, 7-9, 24) were found to be potent inducers of the enzyme, while 5α-substituted derivatives exhibited weak activity. Preliminary studies were performed with compound 29 to evaluate enzyme-inducing capacity in multiple organ sites of BALB/c mice. Significant induction was observed in liver and colon, but not in lung, stomach, or mammary gland. Fil:Veleiro, A.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Cirigliano, A.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Tettamanzi, M.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Burton, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2002 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01633864_v65_n5_p677_Misico http://hdl.handle.net/20.500.12110/paper_01633864_v65_n5_p677_Misico
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 18 hydroxywithanolide d
enzyme inducing agent
jaborosalactone 1
joborosalactone p
reduced nicotinamide adenine dinucleotide (phosphate) dehydrogenase (quinone)
unclassified drug
withanolide derivative
withaphysalin g
withaphysalin h
withaphysalin i
withaphysalin j
animal cell
animal experiment
animal tissue
article
breast
colon
concentration response
controlled study
drug potency
drug structure
enzyme induction
hepatoma cell
liver
lung
mouse
nonhuman
phytochemistry
stomach
Animals
Brassicaceae
Breast
Carcinoma, Hepatocellular
Colon
Enzyme Induction
Inhibitory Concentration 50
Liver
Lung
Mice
Mice, Inbred BALB C
Molecular Structure
Nuclear Magnetic Resonance, Biomolecular
Plants, Medicinal
Quinone Reductases
Solanaceae
Stereoisomerism
Steroids
Stilbenes
Stomach
Tumor Cells, Cultured
Animalia
Murinae
spellingShingle 18 hydroxywithanolide d
enzyme inducing agent
jaborosalactone 1
joborosalactone p
reduced nicotinamide adenine dinucleotide (phosphate) dehydrogenase (quinone)
unclassified drug
withanolide derivative
withaphysalin g
withaphysalin h
withaphysalin i
withaphysalin j
animal cell
animal experiment
animal tissue
article
breast
colon
concentration response
controlled study
drug potency
drug structure
enzyme induction
hepatoma cell
liver
lung
mouse
nonhuman
phytochemistry
stomach
Animals
Brassicaceae
Breast
Carcinoma, Hepatocellular
Colon
Enzyme Induction
Inhibitory Concentration 50
Liver
Lung
Mice
Mice, Inbred BALB C
Molecular Structure
Nuclear Magnetic Resonance, Biomolecular
Plants, Medicinal
Quinone Reductases
Solanaceae
Stereoisomerism
Steroids
Stilbenes
Stomach
Tumor Cells, Cultured
Animalia
Murinae
Veleiro, Adriana Silvia
Cirigliano, Adriana Mónica
Tettamanzi, María Cristina
Burton, Gerardo
Induction of quinone reductase by withanolides
topic_facet 18 hydroxywithanolide d
enzyme inducing agent
jaborosalactone 1
joborosalactone p
reduced nicotinamide adenine dinucleotide (phosphate) dehydrogenase (quinone)
unclassified drug
withanolide derivative
withaphysalin g
withaphysalin h
withaphysalin i
withaphysalin j
animal cell
animal experiment
animal tissue
article
breast
colon
concentration response
controlled study
drug potency
drug structure
enzyme induction
hepatoma cell
liver
lung
mouse
nonhuman
phytochemistry
stomach
Animals
Brassicaceae
Breast
Carcinoma, Hepatocellular
Colon
Enzyme Induction
Inhibitory Concentration 50
Liver
Lung
Mice
Mice, Inbred BALB C
Molecular Structure
Nuclear Magnetic Resonance, Biomolecular
Plants, Medicinal
Quinone Reductases
Solanaceae
Stereoisomerism
Steroids
Stilbenes
Stomach
Tumor Cells, Cultured
Animalia
Murinae
description Thirty-seven naturally occurring withanolides (1-37), previously isolated in our laboratories, were evaluated for their potential to induce quinone reductase with cultured murine hepatoma cells (Hepa 1c1c7). Spiranoid (29, 32) and 18-functionalized withanolides (2-5, 7-9, 24) were found to be potent inducers of the enzyme, while 5α-substituted derivatives exhibited weak activity. Preliminary studies were performed with compound 29 to evaluate enzyme-inducing capacity in multiple organ sites of BALB/c mice. Significant induction was observed in liver and colon, but not in lung, stomach, or mammary gland.
author Veleiro, Adriana Silvia
Cirigliano, Adriana Mónica
Tettamanzi, María Cristina
Burton, Gerardo
author_facet Veleiro, Adriana Silvia
Cirigliano, Adriana Mónica
Tettamanzi, María Cristina
Burton, Gerardo
author_sort Veleiro, Adriana Silvia
title Induction of quinone reductase by withanolides
title_short Induction of quinone reductase by withanolides
title_full Induction of quinone reductase by withanolides
title_fullStr Induction of quinone reductase by withanolides
title_full_unstemmed Induction of quinone reductase by withanolides
title_sort induction of quinone reductase by withanolides
publishDate 2002
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01633864_v65_n5_p677_Misico
http://hdl.handle.net/20.500.12110/paper_01633864_v65_n5_p677_Misico
work_keys_str_mv AT veleiroadrianasilvia inductionofquinonereductasebywithanolides
AT ciriglianoadrianamonica inductionofquinonereductasebywithanolides
AT tettamanzimariacristina inductionofquinonereductasebywithanolides
AT burtongerardo inductionofquinonereductasebywithanolides
_version_ 1768546623943606272