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21-hydroxy-6,19-oxidoprogesterone
Known as:
21-hydroxy-6,19-epoxyprogesterone
, 21OH-6,19OP
, 21OH-6OP
National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
Progesterone
analogs & derivatives
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
21-Hydroxy-6,19-epoxyprogesterone: A Promising Therapeutic Agent and a Molecular Tool for Deciphering Glucocorticoid Action.
A. Pecci
,
L. Álvarez
,
Diego M. Presman
,
G. Burton
Mini-Reviews in Medical Chemistry
2017
Corpus ID: 3995834
Glucocorticoids are steroid hormones that exert most of their effects through their binding to the glucocorticoid receptor (GR…
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Review
2017
Review
2017
21-hydroxy-6,19-epoxyprogesterone: a Promising Therapeutic Agent and a Molecular Tool for Deciphering Glucocorticoid Action.
A. Pecci
,
L. Álvarez
,
Diego M. Presman
,
G. Burton
Mini-Reviews in Medical Chemistry
2017
Corpus ID: 40575135
Glucocorticoids are steroid hormones that exert most of their effects through their binding to the glucocorticoid receptor (GR…
Expand
2014
2014
The rigid steroid 21-hydroxy-6,19-epoxyprogesterone (21OH-6,19OP) is a dissociated glucocorticoid receptor modulator potentially useful as a novel coadjuvant in breast cancer chemotherapy.
Andres J. Orqueda
,
M. Dansey
,
+5 authors
A. Pecci
Biochemical Pharmacology
2014
Corpus ID: 205968701
2010
2010
Insights on Glucocorticoid Receptor Activity Modulation through the Binding of Rigid Steroids
Diego M. Presman
,
L. Álvarez
,
+6 authors
A. Pecci
PLoS ONE
2010
Corpus ID: 12510816
Background The glucocorticoid receptor (GR) is a transcription factor that regulates gene expression in a ligand-dependent…
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2008
2008
Exploring the molecular basis of action of the passive antiglucocorticoid 21-hydroxy-6,19-epoxyprogesterone.
L. Álvarez
,
M. Marti
,
+4 authors
G. Burton
Journal of Medicinal Chemistry
2008
Corpus ID: 32464935
21-Hydroxy-6,19-epoxyprogesterone (21OH-6,19OP) is a selective antiglucocorticoid that lacks the bulky substituent at C-11 found…
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2008
2008
Hemisuccinate of 21‐Hydroxy‐6,19‐Epoxyprogesterone: A Tissue‐Specific Modulator of the Glucocorticoid Receptor
L. Álvarez
,
M. Marti
,
+4 authors
G. Burton
ChemMedChem
2008
Corpus ID: 13035716
The introduction of a hemisuccinate group at the 21‐position of the passive antiglucocorticoid 21OH‐6,19OP leads to a compound…
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Highly Cited
2003
Highly Cited
2003
Mechanism of cortisol/progesterone antagonism in the regulation of 15-hydroxyprostaglandin dehydrogenase activity and messenger ribonucleic acid levels in human chorion and placental trophoblast…
F. Patel
,
J. Funder
,
J. Challis
Journal of Clinical Endocrinology and Metabolism
2003
Corpus ID: 30771514
Prostaglandin dehydrogenase (PGDH) metabolizes prostaglandins (PGs) to render them inactive. We reported previously that cortisol…
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2001
2001
A process for preparing 21-hydroxy-6,19-oxidoprogesterone (21OH-6OP)
G. Burton
,
P. Lantos
,
Silvia Adriana Veleiro
2001
Corpus ID: 189346632
2001
2001
A process for the preparation of 21-hydroxy-6,19-oxidoprogesterone (21OH-6OP)
A. Veleiro
,
G. Burton
,
C. Lantos
2001
Corpus ID: 188036954
1997
1997
21-Hydroxy-6,19-oxidoprogesterone: a novel synthetic steroid with specific antiglucocorticoid properties in the rat.
G. Vicent
,
M. Monteserín
,
A. Veleiro
,
G. Burton
,
C. Lantos
,
M. Galigniana
Molecular Pharmacology
1997
Corpus ID: 5811734
In the rat, the conformationally highly bent steroid 21-hydroxy-6, 19-oxidoprogesterone efficiently displaces [3H]corticosterone…
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