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  • T2315GSK-LSD1 dihydrochlorideGSK-LSD1 2HCl

    GSK-LSD1 2HCl is a specificity irreversible LSD1 inhibitor (IC50: 16 nM). The selectivity of GSK-LSD1 for LSD1 is >1000 fold over other closely related FAD utilizing enzymes (i.e. MAO-A, LSD2, MAO-B).

    价 格:¥电议型 号:T2315产 地:中国大陆

  • T2315GSK-LSD1 dihydrochlorideGSK-LSD1 dihydrochloride,GSK-LSD1 2HCl,

    GSK-LSD1 2HCl is a specificity irreversible LSD1 inhibitor (IC50: 16 nM). The selectivity of GSK-LSD1 for LSD1 is >1000 fold over other closely related FAD utilizing enzymes (i.e. MAO-A, LSD2, MAO-B).

    价 格:¥电议型 号:T2315产 地:美洲

  • T82254GSK-LSD1;化合物 GSK-LSD1GSK-LSD1

    GSK-LSD1, an LSD1 inhibitor, decreases food consumption and body weight while enhancing insulin sensitivity and glycemic regulation in murine obesity models. Additionally, it mitigates non-alcoholic fatty liver disease (NAFLD) and suppresses cytokine release induced by SARS-CoV-2 in COVID-19 peripheral blood mononuclear cells (PBMCs). Furthermore, GSK-LSD1 inhibits the proliferation and spread of cancer [1] [2] [3].

    价 格:¥电议型 号:T82254产 地:中国大陆

  • T2315GSK-LSD1 dihydrochloride;化合物GSK-LSD1 dihydrochlorideGSK-LSD1 (hydrochloride)|||GSK-LSD1 2HCl;GSK-LSD

    GSK-LSD1 dihydrochloride (GSK-LSD1 2HCl) is a specificity irreversible LSD1 inhibitor (IC50: 16 nM). The selectivity of GSK-LSD1 for LSD1 is >1000 fold over other closely related FAD utilizing enzymes (i.e. MAO-A, LSD2, MAO-B).

    价 格:¥电议型 号:T2315产 地:中国大陆

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