Macimorelin Acetate

Macimorelin Acetate features a peptide-derived scaffold designed to probe receptor-interaction determinants. Hydrophobic and heterocyclic elements shape its conformational flexibility. Researchers assess its dynamic structural transitions. Applications include ligand-optimization efforts, structural mapping, and peptide-based chemical biology research.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
Macimorelin Acetate(CAS 945212-59-9)

CAT No: R2695

CAS No:945212-59-9

Synonyms/Alias:Macimorelin acetate;Macrilen;D-87575 acetate;ARD 07 acetate;EP 1572 acetate;UNII-AQZ1003RMG;Macimorelin acetate [USAN];AQZ1003RMG;945212-59-9;AEZS 130;Aib-Trp-gTrp-CHO acetate;Macimorelin (acetate);ARD-07 ACETATE;EP-1572 ACETATE;DTXSID40241516;Macimorelin acetate (USAN);D-Tryptophanamide, 2-methylalanyl-N-((1R)-1-(formylamino)-2-(1H-indol-3-yl)ethyl)-, acetate (1:1);acetic acid;2-amino-N-[(2R)-1-[[(1R)-1-formamido-2-(1H-indol-3-yl)ethyl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]-2-methylpropanamide;N2-(2-amino-2-methylpropanoyl-N1-((1R)-1-formamido-2-(1H-indol-3-yl)ethyl)- D-tryptophanamide acetate;Macrilen (TN);CHEMBL2364617;MACIMORELIN ACETATE [MI];DTXCID70164007;HY-14820A;MACIMORELIN ACETATE [WHO-DD];MACIMORELIN ACETATE [ORANGE BOOK];DA-55160;CS-0027172;D10562;Q27274071;N2-(2-AMINO-2-METHYLPROPANOYL-N1-((1R)-1-FORMAMIDO-2-(1H-INDOL-3-YL)ETHYL)-D-TRYPTOPHANAMIDE ACETATE;

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M.F/Formula
C28H34N6O5
M.W/Mr.
534.6
Sequence
One Letter Code:XW

Macimorelin Acetate, a synthetic ghrelin receptor agonist, is a valuable tool in the field of biochemical research and endocrinology studies. Its unique structure enables it to mimic the activity of endogenous ghrelin, making it highly effective in modulating the growth hormone secretagogue receptor (GHSR). Researchers favor this compound for its stability, specificity, and ability to elicit predictable physiological responses in various experimental models. As a peptide-based molecule, Macimorelin Acetate is easily integrated into diverse assay platforms, allowing for flexible application across multiple domains of life sciences. Its compatibility with both in vitro and in vivo systems further enhances its utility in elucidating complex hormonal pathways and receptor interactions.

Growth Hormone Secretion Studies: Macimorelin Acetate is widely employed in investigations focused on the regulation of growth hormone (GH) release. By binding to the GHSR-1a receptor, it stimulates the secretion of GH from pituitary cells, providing a reliable means to assess the functional status of the somatotropic axis. Researchers use this peptide to explore the physiological mechanisms underlying GH dynamics, evaluate the impact of genetic or pharmacological interventions, and develop new models for studying endocrine disorders. Its robust and reproducible effect on GH release makes it an essential reagent for laboratories seeking to understand the nuances of growth hormone physiology.

Metabolic Research: The application of Macimorelin extends into the realm of metabolic studies, where it serves as a probe for investigating appetite regulation, energy balance, and glucose metabolism. By activating ghrelin signaling pathways, this compound enables scientists to dissect the molecular events that link hormonal activity with metabolic outcomes. It is particularly useful in studies aiming to clarify the role of ghrelin and its analogs in obesity, insulin sensitivity, and lipid metabolism. Through controlled administration in preclinical models, researchers can monitor metabolic shifts and identify potential therapeutic targets for metabolic disorders.

Receptor Pharmacology: Macimorelin Acetate is instrumental in receptor binding and signaling assays designed to characterize the pharmacological properties of ghrelin receptor agonists and antagonists. Its high affinity for the GHSR makes it suitable for competitive binding experiments, receptor activation studies, and downstream signaling analyses. Scientists utilize this peptide to screen novel compounds, map receptor-ligand interactions, and investigate the structural requirements for receptor activation. The insights gained from such studies inform the design of next-generation modulators with improved selectivity and efficacy.

Neuroendocrine Pathway Analysis: Ghrelin and its analogs, including Macimorelin, play a pivotal role in the regulation of neuroendocrine circuits. Researchers leverage this compound to probe the interplay between central and peripheral hormonal signals, particularly in the context of stress response, circadian rhythm, and neuropeptide release. Its use in animal models and cell-based systems facilitates the mapping of signal transduction pathways and the identification of novel neuroendocrine regulators. Such investigations contribute to a deeper understanding of how hormonal signals integrate with neural networks to maintain physiological homeostasis.

Peptide Drug Development: The structural and functional attributes of Macimorelin Acetate make it a reference compound in the development of peptide-based therapeutics targeting the ghrelin receptor. Medicinal chemists and pharmacologists employ it as a benchmark for evaluating the efficacy, stability, and receptor selectivity of new analogs. By serving as a standard in preclinical testing, it helps streamline the optimization of candidate molecules and accelerates the discovery of innovative therapeutic agents. This application underscores the importance of Macimorelin in advancing peptide drug research and expanding the repertoire of bioactive compounds for endocrine and metabolic modulation.

InChI
InChI=1S/C26H30N6O3.C2H4O2/c1-26(2,27)25(35)31-22(11-16-13-28-20-9-5-3-7-18(16)20)24(34)32-23(30-15-33)12-17-14-29-21-10-6-4-8-19(17)21;1-2(3)4/h3-10,13-15,22-23,28-29H,11-12,27H2,1-2H3,(H,30,33)(H,31,35)(H,32,34);1H3,(H,3,4)/t22-,23-;/m1./s1
InChI Key
WVDSKQXKCDZXLH-OHIDFYLOSA-N

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