Spiroxasone: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
 
CSV import
 
Line 1: Line 1:
'''Spiroxasone''' is a [[synthetic compound]] used in the field of [[medicine]] and [[pharmacology]]. It is a [[steroid]] derivative, specifically a [[glucocorticoid]], which is a class of corticosteroids that bind to the glucocorticoid receptor.
{{Short description|A synthetic steroidal antimineralocorticoid and antiandrogen}}
{{Drugbox
| verifiedfields = changed
| verifiedrevid = 477002123
| image = Spiroxasone.png
| image_size = 200px
| image_alt = Chemical structure of Spiroxasone
}}


== History ==
'''Spiroxasone''' is a synthetic [[steroidal antimineralocorticoid]] and [[antiandrogen]] that was developed for the treatment of conditions such as [[hypertension]] and [[heart failure]]. It is a derivative of [[spironolactone]], a well-known [[potassium-sparing diuretic]].


Spiroxasone was first synthesized in the late 20th century as part of a broader effort to develop new and more effective glucocorticoids. The compound was developed by [[pharmaceutical industry|pharmaceutical companies]] seeking to improve upon the anti-inflammatory and immunosuppressive properties of existing glucocorticoids.
==Pharmacology==


== Pharmacology ==
===Mechanism of Action===
Spiroxasone acts as an antagonist of the [[mineralocorticoid receptor]], which is responsible for the effects of [[aldosterone]] in the body. By blocking this receptor, spiroxasone reduces sodium reabsorption and increases potassium retention, leading to a diuretic effect. Additionally, it has antiandrogenic properties, which means it can block the effects of [[androgens]] like [[testosterone]].


As a glucocorticoid, spiroxasone works by binding to the [[glucocorticoid receptor]], a type of [[nuclear receptor]] that is present inside cells. Once bound, the receptor-ligand complex translocates to the cell nucleus, where it regulates the transcription of specific genes. This can lead to a variety of effects, including anti-inflammatory and immunosuppressive actions.
===Pharmacokinetics===
The pharmacokinetic profile of spiroxasone includes its absorption, distribution, metabolism, and excretion. Like other steroidal antimineralocorticoids, it is metabolized in the liver and excreted primarily in the urine.


== Medical Uses ==
==Clinical Use==
Spiroxasone was investigated for use in conditions such as [[hypertension]], [[heart failure]], and [[hirsutism]]. However, it was never marketed, and its clinical use remains limited to research settings.


Spiroxasone has been studied for use in a variety of medical conditions, including [[rheumatoid arthritis]], [[asthma]], and certain [[autoimmune diseases]]. However, its use is currently limited due to potential side effects and the availability of other, more well-established glucocorticoids.
==Side Effects==
Potential side effects of spiroxasone include [[hyperkalemia]], [[gynecomastia]], and [[menstrual irregularities]]. These are similar to those observed with other antimineralocorticoids and antiandrogens.


== Side Effects ==
==Chemical Structure==
[[File:Spiroxasone.png|thumb|right|Chemical structure of Spiroxasone]]
Spiroxasone is a synthetic steroid with a chemical structure similar to that of spironolactone. It contains a lactone ring and a thioacetate group, which are characteristic of this class of compounds.


Like other glucocorticoids, spiroxasone can have a number of side effects. These can include [[osteoporosis]], [[hyperglycemia]], and an increased risk of infection due to its immunosuppressive effects. Long-term use can also lead to [[adrenal insufficiency]], a condition in which the body's own production of glucocorticoids is insufficient.
==Related Compounds==
Spiroxasone is related to other antimineralocorticoids such as [[spironolactone]] and [[eplerenone]]. These compounds share similar mechanisms of action and therapeutic uses.


== See Also ==
==Related pages==
* [[Spironolactone]]
* [[Eplerenone]]
* [[Mineralocorticoid receptor]]
* [[Antiandrogen]]


* [[Glucocorticoid]]
[[Category:Antimineralocorticoids]]
* [[Pharmacology]]
[[Category:Antiandrogens]]
* [[Steroid]]
[[Category:Synthetic steroids]]
 
[[Category:Pharmacology]]
[[Category:Medicine]]
[[Category:Glucocorticoids]]
{{Pharma-stub}}
{{Medicine-stub}}

Latest revision as of 04:02, 13 February 2025

A synthetic steroidal antimineralocorticoid and antiandrogen


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


Spiroxasone is a synthetic steroidal antimineralocorticoid and antiandrogen that was developed for the treatment of conditions such as hypertension and heart failure. It is a derivative of spironolactone, a well-known potassium-sparing diuretic.

Pharmacology[edit]

Mechanism of Action[edit]

Spiroxasone acts as an antagonist of the mineralocorticoid receptor, which is responsible for the effects of aldosterone in the body. By blocking this receptor, spiroxasone reduces sodium reabsorption and increases potassium retention, leading to a diuretic effect. Additionally, it has antiandrogenic properties, which means it can block the effects of androgens like testosterone.

Pharmacokinetics[edit]

The pharmacokinetic profile of spiroxasone includes its absorption, distribution, metabolism, and excretion. Like other steroidal antimineralocorticoids, it is metabolized in the liver and excreted primarily in the urine.

Clinical Use[edit]

Spiroxasone was investigated for use in conditions such as hypertension, heart failure, and hirsutism. However, it was never marketed, and its clinical use remains limited to research settings.

Side Effects[edit]

Potential side effects of spiroxasone include hyperkalemia, gynecomastia, and menstrual irregularities. These are similar to those observed with other antimineralocorticoids and antiandrogens.

Chemical Structure[edit]

Chemical structure of Spiroxasone

Spiroxasone is a synthetic steroid with a chemical structure similar to that of spironolactone. It contains a lactone ring and a thioacetate group, which are characteristic of this class of compounds.

Related Compounds[edit]

Spiroxasone is related to other antimineralocorticoids such as spironolactone and eplerenone. These compounds share similar mechanisms of action and therapeutic uses.

Related pages[edit]