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A subsequent study identified the compound N-(4-(2-(4-(trifluoromethyl)phenyl)thiazol-4-yl)phenyl)acetamide as a notable SARM1 inhibitor, which demonstrated significant efficacy in a mouse model of CIPN (Fig
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Eng., serves as the Deputy Director for Scientific Affairs at the Military Institute of Hygiene and Epidemiology and has participated in the design, synthesis, and study of biologically active peptides, including BPC-157, TB500, and GHK-Cu
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