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Chang, J

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This way, it mirrors the original peptide image to maintain a similar 3D structure and binding properties, while also offering higher resistance to normal proteolytic enzymes, thereby extending its stability and half-life

These structural differences are the basis for comparative structure-activity relationship studies examining how substitution pattern influences adrenergic receptor subtype selectivity and binding affinity across the phenylethanolamine compound series.

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Its compact size makes it ideal for smaller protocols or single-cycle use while still allowing multi-dose withdrawals