Isomerization of bioactive acylhydrazones triggered by light or thiols-Reference-Cited by-同舟云学术

Isomerization of bioactive acylhydrazones triggered by light or thiols

Published:2023-06-12 Issue:9 Volume:15 Page:1285-1295
ISSN:1755-4330
Container-title:Nature Chemistry
language:en
Short-container-title:Nat. Chem.

Author:

Zhang Zhiwei^ORCID,Le Giang N. T.^ORCID,Ge Yang^ORCID,Tang Xiaowen^ORCID,Chen Xin,Ejim Linda,Bordeleau Emily^ORCID,Wright Gerard D.,Burns Darcy C.,Tran Susannah,Axerio-Cilies Peter^ORCID,Wang Yu Tian^ORCID,Dong Mingxin^ORCID,Woolley G. Andrew^ORCID

Publisher

Springer Science and Business Media LLC

Subject

General Chemical Engineering,General Chemistry

Link

https://www.nature.com/articles/s41557-023-01239-5.pdf

Reference93 articles.

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3. Huff, S. E. et al. Structure-guided synthesis and mechanistic studies reveal sweetspots on naphthyl salicyl hydrazone scaffold as non-nucleosidic competitive, reversible inhibitors of human ribonucleotide reductase. J. Med. Chem. 61, 666–680 (2018).

4. Mota Fernandes, C. et al. The future of antifungal drug therapy: novel compounds and targets. Antimicrob. Agents Chemother. https://doi.org/10.1128/AAC.01719-20 (2021).

5. Herschhorn, A. et al. A broad HIV-1 inhibitor blocks envelope glycoprotein transitions critical for entry. Nat. Chem. Biol. 10, 845–852 (2014).

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