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CGRP receptor antagonists block the receptor for calcitonin gene-related peptide (CGRP), a neuropeptide. In 1982 alternative RNA processing of the calcitonin gene was shown to produce CGRP in neural tissue. The receptor is formed by calcitonin receptor-like receptor (CALCRL) together with receptor activity-modifying protein 1 (RAMP1), as described in 1998. CGRP release from trigeminal neurons is studied in migraine models and in neurogenic vasodilation. Olcegepant, telcagepant, MK-3207 and ubrogepant are small-molecule antagonists of this receptor complex. CGRP 8-37 (human) is a truncated peptide antagonist, and α-CGRP(human) serves as the native agonist.
CTR/AMYR modulator-1 is a calcitonin receptor/amylin receptor modulator. It exhibits potential in regulating metabolic pathways and can be employed in the study of metabolic diseases. This compound provides a valuable tool for researchers investigating the molecular mechanisms underlying metabolic disorders and the role of these receptors in energy homeostasis.
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