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Structure-Activity Relationships of the Benzimidazole Opioids: Nitazenes and Piperidinylbenzimidazolones (Cychlorphine, Brorphine, Bezitramide Derivs) [Vol 1]
Structure-Activity Relationships of the Benzimidazole Opioids: Nitazenes and Piperidinylbenzimidazolones (Cychlorphine, Brorphine, Bezitramide Derivs) – [Vol 1: Nitazenes]
Structure-Activity Relationships of the Benzimidazole Opioids: Nitazenes and Piperidinylbenzimidazolones (Cychlorphine, Brorphine, Bezitramide Derivs) [Vol 1]
Structure-Activity Relationships of the Benzimidazole Opioids: Nitazenes and Piperidinylbenzimidazolones (Cychlorphine, Brorphine, Bezitramide Derivs) – [Vol 1: Nitazenes]
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Cychlorphine, a synthetic opioid of the benzimidazolone class, exhibits exceptional potency approximately four times that of fentanyl. The molecule is structured with a unique N(3)-cyanoethyl modification, elevating its efficacy at the mu-opioid receptors, which are pivotal in pain modulation.
Chemical Profile:
- Chemical Formula: C23H25ClN4O
- Molecular Weight: 408.93
Effects and Therapeutic Potential: As an agonist at mu-opioid receptors, Cychlorphine provides profound analgesia, potentially beneficial in settings requiring significant opioid strength with controlled application. The sensation of euphoria and deep sedation are prominent effects, alongside its analgesic properties.
Dosage Considerations: Extreme caution is necessary due to its potency. Administration should be restricted to environments where precise dosing and monitoring are possible, typically starting at the microgram range to avoid adverse effects.
Safety and Side Effects: Users may experience typical opioid-related side effects such as nausea, respiratory depression, and sedation. Its potential for dependence and abuse is significant, necessitating stringent controls.
Harm Reduction Strategies: Ensuring the availability of naloxone kits, training in overdose response, and strict regulatory compliance are vital for minimizing risks associated with its use.
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Cychlorphine is an innovative benzimidazolone-based opioid, known for its exceptional potency, about four times stronger than fentanyl. This research chemical, with its profound efficacy at mu-opioid receptors, is primarily used for scientific studies aimed at understanding pain mechanisms and developing new analgesics.
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Cychlorphine is an advanced synthetic opioid analgesic characterized by its unique chemical structure, C23H25ClN4O, and a molecular weight of 408.93. This compound, a benzimidazolone derivative, is noted for its significant potency, being approximately four times stronger than fentanyl. The distinctiveness of Cychlorphine lies in its N(3)-cyanoethyl modification within the benzimidazolone series, which enhances mu-opioid receptor (MOR) activity beyond typical opioid analogs.
Pharmacodynamics and Effects: Cychlorphine exerts its effects by binding to and activating the mu-opioid receptors located in the brain, spinal cord, and other tissues, leading to pronounced analgesic effects, euphoria, and sedation. Its receptor affinity contributes to its high potency and effectiveness as an analgesic.
Dosage and Administration: Due to its high potency, Cychlorphine should be administered with caution. Dosage should start at microgram levels, with careful titration according to response and tolerance. Healthcare professionals should ensure precision in dosing to avoid overdose.
Side Effects: Common side effects include but are not limited to nausea, vomiting, constipation, and drowsiness. Severe side effects might include respiratory depression, profound sedation, and hypotension. Due to its potency, there is a significant risk of addiction and dependence.
Harm Reduction: To mitigate risks, Cychlorphine should be used strictly in controlled settings with appropriate monitoring. Naloxone should be available as an antidote for opioid overdose. Users should be educated on the signs of overdose and the importance of adhering to prescribed dosages.
Regulatory Status: Currently, Cychlorphine is classified under research substances and is not approved for medical use outside of research settings. It is crucial for research and handling to adhere to legal and safety regulations to prevent misuse.
This description is a concise summary and does not delve into all complexities or potential applications of Cychlorphine. For a detailed exploration, further reading and consultation with specialized literature and experts are recommended.
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