Amine substitution of quinazolinones leads to selective nanomolar AChE inhibitors with ‘inverted’ binding mode.

MLA

Darras, Fouad H., et al. “Amine Substitution of Quinazolinones Leads to Selective Nanomolar AChE Inhibitors with ‘Inverted’ Binding Mode.” Bioorganic & Medicinal Chemistry, vol. 22, no. 17, Sept. 2014, pp. 4867–81. EBSCOhost, https://doi.org/10.1016/j.bmc.2014.06.045.

APA

Darras, F. H., Wehle, S., Huang, G., Sotriffer, C. A., & Decker, M. (2014). Amine substitution of quinazolinones leads to selective nanomolar AChE inhibitors with ‘inverted’ binding mode. Bioorganic & Medicinal Chemistry, 22(17), 4867–4881. https://doi.org/10.1016/j.bmc.2014.06.045

Chicago

Darras, Fouad H., Sarah Wehle, Guozheng Huang, Christoph A. Sotriffer, and Michael Decker. 2014. “Amine Substitution of Quinazolinones Leads to Selective Nanomolar AChE Inhibitors with ‘Inverted’ Binding Mode.” Bioorganic & Medicinal Chemistry 22 (17): 4867–81. doi:10.1016/j.bmc.2014.06.045.