微尺度热泳
放射合成
化学
小分子
体内
肽
立体化学
分子
生物化学
有机化学
生物
生物技术
作者
Jenilee D. Woodfield,Atul Bhardwaj,Cody Bergman,Frank Wuest
标识
DOI:10.1002/cmdc.202100544
摘要
Eleven small-molecular-weight compounds and three cyclic peptides were synthesized and evaluated for binding to hypoxia-inducible factor-1α (HIF-1α). Microscale thermophoresis analysis identified peptide [19 F]SFB-link-c-(Ppg)LLFVY 3 and small-molecule inhibitor 5 as potent HIF-1α binding compounds with KD values of 0.46±0.2 μM and 7.8±3.4 μM, respectively. Both compounds represent novel HIF-1α-targeting compounds that are predicted to interact with the PAS-B region of HIF-1α, as confirmed with molecular docking studies. Lead structures 3 and 5 were further radiolabelled with fluorine-18 for positron emission tomography (PET) imaging agents targeting HIF-1α in vivo.
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