R. C. Brothers

Structure-Activity Relationships of the MEPicides: N-Acyl and O-Linked Analogs of FR900098 as Inhibitors of Dxr from Mycobacterium tuberculosis and Yersinia pestis.

Rachel L. Edwards, A. Haymond, H. Boshoff, 2016, ACS infectious diseases.

MEPicides: potent antimalarial prodrugs targeting isoprenoid biosynthesis

K. Williamson, P. Hruz, Rachel L. Edwards, 2017, Scientific Reports.

MEPicides: α,β-Unsaturated Fosmidomycin Analogues as DXR Inhibitors against Malaria.

Rachel L. Edwards, S. Alvarez, H. Boshoff, 2018, Journal of medicinal chemistry.

Potent, specific MEPicides for treatment of zoonotic staphylococci

C. Burnham, Justin J. Miller, J. Jez, 2019, bioRxiv.

Mechanism of Action of N-Acyl and N-Alkoxy Fosmidomycin Analogs: Mono- and Bisubstrate Inhibition of IspC from Plasmodium falciparum, a Causative Agent of Malaria

H. Ball, Misgina B Girma, R. Couch, 2021, ACS omega.

Design, synthesis, and evaluation of substituted nicotinamide adenine dinucleotide (NAD+) synthetase inhibitors as potential antitubercular agents.

B. Gerratana, M. Kneen, H. Boshoff, 2017, Bioorganic & medicinal chemistry letters.

MEPicides: α,β-unsaturated Fosmidomycin N-Acyl Analogs as Efficient Inhibitors of Plasmodium falciparum 1-Deoxy-d-xylulose-5-phosphate reductoisomerase.

Allyson L Dailey, Rachel L. Edwards, H. Boshoff, 2023, ACS infectious diseases.

Design, synthesis, and evaluation of substituted nicotinamide adenine dinucleotide (NAD+) synthetase inhibitors as potential antitubercular agents.

B. Gerratana, M. Kneen, H. Boshoff, 2017, Bioorganic & Medicinal Chemistry Letters.