Β-Hydroxyfentanyl
Synthetic opioid analgesic
Β-Hydroxyfentanyl | |
---|---|
![]() | |
INN | |
Drug class | |
Routes of administration | |
Pregnancy category | |
Bioavailability | |
Metabolism | |
Elimination half-life | |
Excretion | |
Legal status | |
CAS Number | |
PubChem | |
DrugBank | |
ChemSpider | |
KEGG |
β-Hydroxyfentanyl is a potent synthetic opioid analgesic, closely related to fentanyl. It is part of the fentanyl family of drugs, which are known for their powerful analgesic properties and potential for abuse.
Chemical Structure and Properties[edit | edit source]
β-Hydroxyfentanyl is chemically similar to fentanyl, with the addition of a hydroxyl group at the beta position of the propanamide chain. This modification can influence the drug's pharmacokinetics and pharmacodynamics, potentially altering its potency and duration of action compared to fentanyl.
The chemical structure of β-Hydroxyfentanyl is characterized by a piperidine ring, a phenethyl group, and a phenylacetamide moiety. The presence of the hydroxyl group may affect the drug's solubility and interaction with opioid receptors.
Pharmacology[edit | edit source]
β-Hydroxyfentanyl acts primarily as an agonist at the mu-opioid receptor, similar to other opioids in the fentanyl class. This interaction is responsible for its analgesic effects, as well as its potential for respiratory depression, euphoria, and addiction.
The addition of the hydroxyl group may influence the drug's binding affinity and efficacy at the opioid receptor, although specific pharmacological data on β-Hydroxyfentanyl is limited compared to fentanyl.
Medical Use and Regulation[edit | edit source]
Due to its potency and risk of abuse, β-Hydroxyfentanyl is not commonly used in clinical practice. It is primarily of interest in research settings and is subject to strict regulatory controls in many countries.
Toxicity and Overdose[edit | edit source]
As with other potent opioids, β-Hydroxyfentanyl carries a significant risk of overdose, which can lead to respiratory depression, coma, and death. The presence of the hydroxyl group does not significantly mitigate these risks, and caution is advised when handling or studying this compound.
Synthesis[edit | edit source]
The synthesis of β-Hydroxyfentanyl involves the modification of the fentanyl molecule to introduce the hydroxyl group. This process requires specialized knowledge in organic chemistry and access to controlled substances.
Related Compounds[edit | edit source]
β-Hydroxyfentanyl is part of a broader class of fentanyl analogs, which include:
These compounds vary in their potency, duration of action, and clinical applications.
Related Pages[edit | edit source]
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD's Wellness Encyclopedia |
Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
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
Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD