Bilaid C is a tetrapeptide recognized for its selective agonist activity at the μ-Opioid Receptor (MOPr), with a binding affinity (Ki) of 210 nM for the human receptor. Isolated from the Australian estuarine strain of Penicillium sp. MST-MF667, Bilaid C demonstrates significant potential in research applications targeting pain modulation, addiction, and opioid receptor signaling pathways. Its molecular properties make it a valuable tool for investigating the role of MOPr in various biological processes.
Bilaid C is a tetrapeptide recognized for its selective agonist activity at the μ-Opioid Receptor (MOPr), with a binding affinity (Ki) of 210 nM for the human receptor. Isolated from the Australian estuarine strain of Penicillium sp. MST-MF667, Bilaid C demonstrates significant potential in research applications targeting pain modulation, addiction, and opioid receptor signaling pathways. Its molecular properties make it a valuable tool for investigating the role of MOPr in various biological processes.
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