| Literature DB >> 30681236 |
Hui Xing1, Sevan D Houston1, Xuejie Chen2, Sussan Ghassabian3, Tyler Fahrenhorst-Jones1, Andy Kuo3, Cody-Ellen P Murray4, Kyna-Anne Conn5, Kara N Jaeschke5, Da-Yun Jin2, Cielo Pasay6, Paul V Bernhardt1, Jed M Burns1, John Tsanaktsidis7, G Paul Savage7, Glen M Boyle6, James J De Voss1, James McCarthy6, Gimme H Walter4, Thomas H J Burne5, Maree T Smith3, Jian-Ke Tie2, Craig M Williams1.
Abstract
Cubane was recently validated as a phenyl ring (bio)isostere, but highly strained caged carbocyclic systems lack π character, which is often critical for mediating key biological interactions. This electronic property restriction associated with cubane has been addressed herein with cyclooctatetraene (COT), using known pharmaceutical and agrochemical compounds as templates. COT either outperformed or matched cubane in multiple cases suggesting that versatile complementarity exists between the two systems for enhanced bioactive molecule discovery.Entities:
Keywords: agrochemicals; bioisostere; cubanes; cyclooctatetraenes; pharmaceuticals
Year: 2019 PMID: 30681236 PMCID: PMC6436534 DOI: 10.1002/chem.201806277
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236