2-Hydroxyestrone: Difference between revisions
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{{DISPLAYTITLE:2-Hydroxyestrone}} | {{DISPLAYTITLE:2-Hydroxyestrone}} | ||
== 2-Hydroxyestrone == | |||
[[File:2-Hydroxyestrone.svg|thumb|right|Chemical structure of 2-Hydroxyestrone]] | |||
'''2-Hydroxyestrone''' is a [[metabolite]] of the [[estrogen]] hormone [[estrone]]. It is one of the major [[catechol estrogens]], which are hydroxylated derivatives of estrogens. The hydroxylation occurs at the C2 position of the [[steroid]] ring structure, resulting in the formation of 2-hydroxyestrone. | |||
2-Hydroxyestrone is | |||
== | == Biochemistry == | ||
2-Hydroxyestrone is | 2-Hydroxyestrone is formed from estrone through the action of the enzyme [[cytochrome P450]] 1A1 (CYP1A1) and other related enzymes. This hydroxylation process is part of the [[phase I metabolism]] of estrogens, which prepares them for further metabolism and excretion. | ||
Once formed, 2-hydroxyestrone can undergo further metabolism to form [[2-methoxyestrone]] through the action of the enzyme [[catechol-O-methyltransferase]] (COMT). This methylation step is important for the detoxification and elimination of catechol estrogens from the body. | |||
== | == Biological Activity == | ||
2-Hydroxyestrone | 2-Hydroxyestrone has been studied for its potential role in modulating estrogenic activity in the body. Unlike estrone and [[estradiol]], which are potent estrogens, 2-hydroxyestrone has relatively weak estrogenic activity. It is thought to act as an [[antiestrogen]] in some tissues, potentially influencing the risk of estrogen-related diseases such as [[breast cancer]]. | ||
==Related | == Clinical Significance == | ||
The balance between different estrogen metabolites, including 2-hydroxyestrone and [[16_-hydroxyestrone]], has been investigated for its potential implications in health and disease. A higher ratio of 2-hydroxyestrone to 16_-hydroxyestrone is sometimes considered favorable, as 2-hydroxyestrone is thought to be less carcinogenic. | |||
== Related Compounds == | |||
* [[Estrone]] | * [[Estrone]] | ||
* [[Estrogen]] | * [[Estradiol]] | ||
* [[Catechol | * [[2-Methoxyestrone]] | ||
* [[16_-Hydroxyestrone]] | |||
== Related Pages == | |||
* [[Estrogen metabolism]] | |||
* [[Catechol estrogens]] | |||
* [[Breast cancer]] | * [[Breast cancer]] | ||
[[Category:Estrogens]] | [[Category:Estrogens]] | ||
[[Category:Steroid hormones]] | [[Category:Steroid hormones]] | ||
[[Category: | [[Category:Metabolites]] | ||
Latest revision as of 11:35, 15 February 2025
2-Hydroxyestrone[edit]
2-Hydroxyestrone is a metabolite of the estrogen hormone estrone. It is one of the major catechol estrogens, which are hydroxylated derivatives of estrogens. The hydroxylation occurs at the C2 position of the steroid ring structure, resulting in the formation of 2-hydroxyestrone.
Biochemistry[edit]
2-Hydroxyestrone is formed from estrone through the action of the enzyme cytochrome P450 1A1 (CYP1A1) and other related enzymes. This hydroxylation process is part of the phase I metabolism of estrogens, which prepares them for further metabolism and excretion.
Once formed, 2-hydroxyestrone can undergo further metabolism to form 2-methoxyestrone through the action of the enzyme catechol-O-methyltransferase (COMT). This methylation step is important for the detoxification and elimination of catechol estrogens from the body.
Biological Activity[edit]
2-Hydroxyestrone has been studied for its potential role in modulating estrogenic activity in the body. Unlike estrone and estradiol, which are potent estrogens, 2-hydroxyestrone has relatively weak estrogenic activity. It is thought to act as an antiestrogen in some tissues, potentially influencing the risk of estrogen-related diseases such as breast cancer.
Clinical Significance[edit]
The balance between different estrogen metabolites, including 2-hydroxyestrone and 16_-hydroxyestrone, has been investigated for its potential implications in health and disease. A higher ratio of 2-hydroxyestrone to 16_-hydroxyestrone is sometimes considered favorable, as 2-hydroxyestrone is thought to be less carcinogenic.
