4.6 Article

Antiangiogenic Activity and in Silico Cereblon Binding Analysis of Novel Thalidomide Analogs

期刊

MOLECULES
卷 25, 期 23, 页码 -

出版社

MDPI
DOI: 10.3390/molecules25235683

关键词

angiogenesis; cereblon; docking; structure– activity relationships; thalidomide

资金

  1. Intramural Research Program of the Center for Cancer Research, National Cancer Institute [ZIA SC006538]
  2. Frederick National Laboratory for Cancer Research, National Institutes of Health [HHSN261200800001E]
  3. Intramural Research Program of the National Institute on Aging, National Institutes of Health
  4. Wellcome Trust-NIH PhD Studentship [098252/Z/12/Z]
  5. Wellcome Trust [098252/Z/12/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

Due to its antiangiogenic and anti-immunomodulatory activity, thalidomide continues to be of clinical interest despite its teratogenic actions, and efforts to synthesize safer, clinically active thalidomide analogs are continually underway. In this study, a cohort of 27 chemically diverse thalidomide analogs was evaluated for antiangiogenic activity in an ex vivo rat aorta ring assay. The protein cereblon has been identified as the target for thalidomide, and in silico pharmacophore analysis and molecular docking with a crystal structure of human cereblon were used to investigate the cereblon binding abilities of the thalidomide analogs. The results suggest that not all antiangiogenic thalidomide analogs can bind cereblon, and multiple targets and mechanisms of action may be involved.

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