Dimethyldienolone: Difference between revisions

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'''Dimethyldienolone''' is a [[synthetic]], [[steroid|steroidal]] [[androgen]] that is part of the [[family (biology)|family]] of [[anabolic steroid|anabolic steroids]]. It is also known as 7α,17α-dimethyl-δ1-testosterone or as 7α,17α-dimethylestr-4-en-17β-ol-3-one.
{{DISPLAYTITLE:Dimethyldienolone}}


==Chemistry==
== Overview ==
Dimethyldienolone is a [[synthetic]] [[estrane]] steroid and a [[derivative]] of [[testosterone]]. It is more specifically a derivative of [[nandrolone]] (19-nortestosterone) or more precisely, [[nandrolone (17β-hydroxyestr-4-en-3-one)]].
'''Dimethyldienolone''' is a synthetic [[anabolic steroid]] and a derivative of [[nandrolone]]. It is known for its potent [[androgenic]] and [[anabolic]] effects. Dimethyldienolone is not approved for medical use and is primarily encountered in the context of [[performance-enhancing drugs]].


==Pharmacology==
== Chemical Structure ==
As an [[androgen]] and [[anabolic steroid]], dimethyldienolone has the ability to increase [[protein synthesis]] in the body, leading to increased muscle mass and strength. It also has the potential to promote secondary male sexual characteristics such as increased body hair and a deepening of the voice.
[[File:Dimethyldienolone.svg|thumb|right|Chemical structure of Dimethyldienolone]]
Dimethyldienolone is chemically classified as a 19-nortestosterone derivative. Its structure is characterized by the presence of a 17_-methyl group and a 9,11-diene configuration, which contribute to its high potency and resistance to metabolic breakdown.


==Side Effects==
== Mechanism of Action ==
Like all anabolic steroids, dimethyldienolone has potential side effects. These can include [[acne]], [[hair loss]], [[gynecomastia]], and increased aggression. It can also have serious health risks such as liver damage, cardiovascular disease, and reproductive system disorders.
Dimethyldienolone exerts its effects by binding to the [[androgen receptor]], which leads to the activation of [[gene transcription]] and subsequent protein synthesis. This results in increased muscle mass and strength, as well as other androgenic effects such as the development of male secondary sexual characteristics.


==Legal Status==
== Pharmacokinetics ==
In many countries, including the United States, dimethyldienolone is classified as a [[controlled substance]]. This means it is illegal to possess, distribute, or manufacture without a prescription or license.
The pharmacokinetics of Dimethyldienolone involve its absorption, distribution, metabolism, and excretion. Due to its methylation at the 17_ position, it is orally active and resistant to hepatic metabolism, allowing it to maintain its activity when administered orally.


==See Also==
== Side Effects ==
The use of Dimethyldienolone can lead to a range of side effects, particularly due to its androgenic properties. These may include:
* [[Acne]]
* [[Hirsutism]]
* [[Gynecomastia]]
* [[Hepatotoxicity]]
* [[Cardiovascular disease]]
 
== Legal Status ==
Dimethyldienolone is classified as a controlled substance in many countries due to its potential for abuse and adverse health effects. It is banned by most sports organizations and is included in the list of prohibited substances by the [[World Anti-Doping Agency]].
 
== Related Compounds ==
Dimethyldienolone is related to other anabolic steroids such as [[nandrolone]], [[trenbolone]], and [[methandrostenolone]]. These compounds share similar mechanisms of action and effects but differ in their chemical structure and potency.
 
== Related Pages ==
* [[Anabolic steroid]]
* [[Anabolic steroid]]
* [[Androgen]]
* [[Androgen receptor]]
* [[Performance-enhancing drugs]]
* [[Nandrolone]]
* [[Nandrolone]]
* [[Testosterone]]


[[Category:Anabolic steroids]]
[[Category:Anabolic steroids]]
[[Category:Androgens]]
[[Category:Controlled substances]]
{{medicine-stub}}

Latest revision as of 11:56, 15 February 2025


Overview[edit]

Dimethyldienolone is a synthetic anabolic steroid and a derivative of nandrolone. It is known for its potent androgenic and anabolic effects. Dimethyldienolone is not approved for medical use and is primarily encountered in the context of performance-enhancing drugs.

Chemical Structure[edit]

Chemical structure of Dimethyldienolone

Dimethyldienolone is chemically classified as a 19-nortestosterone derivative. Its structure is characterized by the presence of a 17_-methyl group and a 9,11-diene configuration, which contribute to its high potency and resistance to metabolic breakdown.

Mechanism of Action[edit]

Dimethyldienolone exerts its effects by binding to the androgen receptor, which leads to the activation of gene transcription and subsequent protein synthesis. This results in increased muscle mass and strength, as well as other androgenic effects such as the development of male secondary sexual characteristics.

Pharmacokinetics[edit]

The pharmacokinetics of Dimethyldienolone involve its absorption, distribution, metabolism, and excretion. Due to its methylation at the 17_ position, it is orally active and resistant to hepatic metabolism, allowing it to maintain its activity when administered orally.

Side Effects[edit]

The use of Dimethyldienolone can lead to a range of side effects, particularly due to its androgenic properties. These may include:

Legal Status[edit]

Dimethyldienolone is classified as a controlled substance in many countries due to its potential for abuse and adverse health effects. It is banned by most sports organizations and is included in the list of prohibited substances by the World Anti-Doping Agency.

Related Compounds[edit]

Dimethyldienolone is related to other anabolic steroids such as nandrolone, trenbolone, and methandrostenolone. These compounds share similar mechanisms of action and effects but differ in their chemical structure and potency.

Related Pages[edit]