Pentafluranol: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
Tags: mobile edit mobile web edit
 
CSV import
Line 1: Line 1:
'''Pentafluranol''' is a [[chemical compound]] that belongs to the class of [[organic compounds]] known as [[fluorocarbons]]. It is a type of [[fluoroalcohol]] that contains five [[fluorine]] atoms and one [[hydroxyl]] group.  
{{Short description|A synthetic nonsteroidal estrogen}}
{{Drugbox
| verifiedfields = changed
| verifiedrevid = 477241123
| image = Pentafluranol.svg
| image2 = <!-- Another image if available -->
| width = 200px
}}


==Chemical Structure==
'''Pentafluranol''' is a synthetic nonsteroidal [[estrogen]] that was developed for potential use in [[hormone replacement therapy]] and other estrogen-related treatments. It belongs to a class of compounds known as [[stilbestrol]] derivatives, which are characterized by their structural similarity to the natural hormone [[estradiol]].
The chemical structure of Pentafluranol consists of a carbon backbone with five fluorine atoms and one hydroxyl group attached. The presence of fluorine atoms gives the compound its unique properties, such as high [[electronegativity]], low [[polarizability]], and high [[thermal stability]]. The hydroxyl group contributes to the compound's [[polarity]] and ability to form [[hydrogen bonds]].


==Synthesis==
==Chemical structure and properties==
The synthesis of Pentafluranol typically involves the reaction of a [[pentachlorophenol]] with a [[fluorinating agent]], such as [[hydrogen fluoride]] or [[antimony trifluoride]]. The reaction proceeds via a [[nucleophilic substitution]] mechanism, where the chlorine atoms are replaced by fluorine atoms.
Pentafluranol is a derivative of [[diethylstilbestrol]], a well-known synthetic estrogen. The chemical structure of pentafluranol includes multiple fluorine atoms, which are believed to influence its biological activity and pharmacokinetics. The presence of these fluorine atoms may enhance the compound's [[lipophilicity]], potentially affecting its distribution and metabolism in the body.


==Properties==
==Mechanism of action==
Pentafluranol is a colorless, crystalline solid at room temperature. It has a high melting point due to the strong [[intermolecular forces]] between the molecules, which are a result of the high electronegativity of the fluorine atoms and the ability of the hydroxyl group to form hydrogen bonds. Pentafluranol is also highly resistant to [[thermal degradation]] and [[chemical attack]], making it suitable for use in various industrial applications.
As an estrogen, pentafluranol exerts its effects by binding to and activating the [[estrogen receptor]]s, which are present in various tissues throughout the body. This activation leads to the modulation of gene expression and the regulation of numerous physiological processes, including the development and maintenance of female secondary sexual characteristics, regulation of the menstrual cycle, and maintenance of bone density.


==Applications==
==Potential therapeutic uses==
Due to its unique properties, Pentafluranol finds use in a variety of applications. It is used as a [[flame retardant]] in the production of [[polymers]] and [[plastics]], due to its high thermal stability and ability to release fluorine atoms upon heating. It is also used as a [[solvent]] in the [[pharmaceutical industry]] due to its polarity and ability to form hydrogen bonds.
Pentafluranol was investigated for its potential use in hormone replacement therapy, particularly for the treatment of symptoms associated with [[menopause]], such as [[hot flashes]], [[osteoporosis]], and [[vaginal atrophy]]. However, like many synthetic estrogens, its development and use have been limited due to concerns about safety and side effects.


==Safety==
==Safety and side effects==
Like all fluorocarbons, Pentafluranol should be handled with care. It can cause irritation to the skin and eyes, and prolonged exposure can lead to more serious health effects. Proper [[safety measures]] should be taken when handling this compound, including the use of [[personal protective equipment]] and adequate ventilation.
The use of synthetic estrogens, including pentafluranol, has been associated with an increased risk of certain adverse effects, such as [[thromboembolism]], [[breast cancer]], and [[endometrial cancer]]. These risks have led to caution in the use of such compounds, particularly in long-term therapy.


==See Also==
==Related compounds==
* [[Fluorocarbons]]
Pentafluranol is related to other synthetic estrogens, such as [[diethylstilbestrol]] and [[hexestrol]]. These compounds share similar mechanisms of action but may differ in their pharmacokinetic properties and safety profiles.
* [[Fluoroalcohols]]
* [[Pentachlorophenol]]
* [[Hydrogen fluoride]]
* [[Antimony trifluoride]]


[[Category:Chemical compounds]]
==Related pages==
[[Category:Organic compounds]]
* [[Estrogen]]
[[Category:Fluorocarbons]]
* [[Hormone replacement therapy]]
[[Category:Fluoroalcohols]]
* [[Diethylstilbestrol]]
{{Chem-stub}}
* [[Synthetic estrogen]]
 
[[Category:Synthetic estrogens]]
[[Category:Stilbestrol derivatives]]

Revision as of 10:56, 15 February 2025

A synthetic nonsteroidal estrogen


Pentafluranol
INN
Drug class
Routes of administration
Pregnancy category
Bioavailability
Metabolism
Elimination half-life
Excretion
Legal status
CAS Number
PubChem
DrugBank
ChemSpider
KEGG


Pentafluranol is a synthetic nonsteroidal estrogen that was developed for potential use in hormone replacement therapy and other estrogen-related treatments. It belongs to a class of compounds known as stilbestrol derivatives, which are characterized by their structural similarity to the natural hormone estradiol.

Chemical structure and properties

Pentafluranol is a derivative of diethylstilbestrol, a well-known synthetic estrogen. The chemical structure of pentafluranol includes multiple fluorine atoms, which are believed to influence its biological activity and pharmacokinetics. The presence of these fluorine atoms may enhance the compound's lipophilicity, potentially affecting its distribution and metabolism in the body.

Mechanism of action

As an estrogen, pentafluranol exerts its effects by binding to and activating the estrogen receptors, which are present in various tissues throughout the body. This activation leads to the modulation of gene expression and the regulation of numerous physiological processes, including the development and maintenance of female secondary sexual characteristics, regulation of the menstrual cycle, and maintenance of bone density.

Potential therapeutic uses

Pentafluranol was investigated for its potential use in hormone replacement therapy, particularly for the treatment of symptoms associated with menopause, such as hot flashes, osteoporosis, and vaginal atrophy. However, like many synthetic estrogens, its development and use have been limited due to concerns about safety and side effects.

Safety and side effects

The use of synthetic estrogens, including pentafluranol, has been associated with an increased risk of certain adverse effects, such as thromboembolism, breast cancer, and endometrial cancer. These risks have led to caution in the use of such compounds, particularly in long-term therapy.

Related compounds

Pentafluranol is related to other synthetic estrogens, such as diethylstilbestrol and hexestrol. These compounds share similar mechanisms of action but may differ in their pharmacokinetic properties and safety profiles.

Related pages