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Description

doi: 10.4088/JCP.15r09984

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2021 Nov;49(11):1441-1442

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Fue diseado como agonista selectivo del receptor de ghrelina (GHSR1a) con la promesa especfica de liberar GH endgena sin activar simultneamente los ejes ACTH/cortisol y prolactina que acompaaban a GHRP-2, GHRP-6 y Hexarelin

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For EPR determination, CuSAE was added to a HAC-NaAC buffer (pH 6.0) containing 1.0 mM H 2 O 2 and 100 M DMPO

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