2,4-Dinitrophenylmorphine
From WikiMD's Wellness Encyclopedia
2,4-Dinitrophenylmorphine is a chemical compound that belongs to the class of organic molecules known as nitrophenols. Specifically, it is a derivative of morphine, a potent opioid analgesic, where the morphine molecule has been chemically modified by the addition of two nitro groups at the 2 and 4 positions of the phenyl ring. This modification significantly alters the properties and biological activity of the original morphine molecule.
Chemistry[edit | edit source]
2,4-Dinitrophenylmorphine is synthesized through a process of nitration, where morphine undergoes a chemical reaction to introduce nitro groups (-NO2) into its molecular structure. The presence of these nitro groups on the morphine backbone is what distinguishes 2,4-Dinitrophenylmorphine from its parent compound and other morphine derivatives.
Pharmacology[edit | edit source]
The pharmacological profile of 2,4-Dinitrophenylmorphine is complex due to the modifications of the morphine molecule. While morphine primarily acts as an agonist at the mu-opioid receptor, the introduction of nitro groups may affect its affinity and efficacy at this receptor, potentially altering its analgesic properties and side effect profile. The exact pharmacological effects of 2,4-Dinitrophenylmorphine, including its potency, efficacy, and safety, would require detailed empirical studies to fully understand.
Potential Applications and Concerns[edit | edit source]
Given its structural relation to morphine, 2,4-Dinitrophenylmorphine might have potential applications in pain management. However, the modification could also impact the drug's pharmacokinetics, possibly affecting its absorption, distribution, metabolism, and excretion (ADME) profile. Additionally, the presence of nitro groups raises concerns about the compound's toxicity, as nitro compounds can sometimes be harmful or have unpredictable effects in biological systems.
Legal Status[edit | edit source]
The legal status of 2,4-Dinitrophenylmorphine would likely depend on its classification under various national and international drug control laws. Given its derivation from morphine, a controlled substance in many jurisdictions, it might be subject to similar regulations aimed at preventing abuse and ensuring safe medical use.
Research and Development[edit | edit source]
Research into 2,4-Dinitrophenylmorphine and similar compounds is important for the development of new analgesics that can provide effective pain relief with fewer side effects or reduced potential for abuse. However, the development of such drugs must be accompanied by thorough preclinical and clinical testing to ensure their safety and efficacy for human use.
Navigation: Wellness - Encyclopedia - Health topics - Disease Index - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes
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 is not a substitute for professional medical advice. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates 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