化学
生物利用度
体内
前列腺素
再生(生物学)
药理学
离体
脱氢酶
前列腺素E2
生物化学
酶
体外
内分泌学
细胞生物学
生物
生物技术
作者
Bin Hu,Kosuke Toda,Xiaoyu Wang,Monika I. Antczak,Julianne Smith,Sophie Geboers,Gen Nishikawa,Hongyun Li,Dawn Dawson,Stephen P. Fink,Amar B. Desai,Noelle S. Williams,Sanford D. Markowitz,Joseph M. Ready
标识
DOI:10.1021/acs.jmedchem.2c01299
摘要
15-Prostaglandin dehydrogenase (15-PGDH) regulates the concentration of prostaglandin E2 in vivo. Inhibitors of 15-PGDH elevate PGE2 levels and promote tissue repair and regeneration. Here, we describe a novel class of quinoxaline amides that show potent inhibition of 15-PGDH, good oral bioavailability, and protective activity in mouse models of ulcerative colitis and recovery from bone marrow transplantation.
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