25I-NB3OMe
25I-NB3OMe[edit]
25I-NB3OMe, also known as 2C-I-NBOMe, is a synthetic psychedelic compound that belongs to the NBOMe class. It is a derivative of the phenethylamine 2C-I and is known for its potent hallucinogenic effects.
Chemical Structure and Properties[edit]
25I-NB3OMe is chemically related to the 2C family of phenethylamines, specifically 2C-I. The compound is characterized by the presence of a methoxy group at the 3-position of the benzene ring, which is a modification from the parent compound 2C-I. This modification significantly increases the compound's affinity for the 5-HT2A receptor, which is believed to be responsible for its psychedelic effects.
Pharmacology[edit]
The primary mechanism of action for 25I-NB3OMe is its agonistic activity at the 5-HT2A receptor, a subtype of the serotonin receptor that is commonly associated with the effects of classic psychedelics such as LSD and psilocybin. The compound's high potency and efficacy at this receptor make it a powerful hallucinogen, even at low doses.
Effects[edit]
Users of 25I-NB3OMe report a range of effects, including visual and auditory hallucinations, altered perception of time, and changes in mood and thought patterns. The intensity and duration of these effects can vary significantly depending on the dose and individual sensitivity.
Risks and Safety[edit]
25I-NB3OMe is associated with several risks, particularly due to its high potency. Overdose can lead to severe adverse effects, including vasoconstriction, hypertension, and tachycardia. There have been reports of fatalities associated with the use of NBOMe compounds, often due to misidentification or improper dosing.
Legal Status[edit]
The legal status of 25I-NB3OMe varies by country. In many jurisdictions, it is classified as a controlled substance due to its potential for abuse and lack of accepted medical use. Users should be aware of the legal implications of possessing or distributing this compound.
Related Compounds[edit]
Related Pages[edit]
Medical Disclaimer: WikiMD is for informational purposes only and is not a substitute for professional medical advice. Content may be inaccurate or outdated and should not be used for diagnosis or treatment. Always consult your healthcare provider for medical decisions. Verify information with trusted sources such as CDC.gov and NIH.gov. By using this site, you agree that WikiMD is not liable for any outcomes related to its content. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
