David H. Peyton

Affiliations: 
Chemistry Portland State University, Portland, OR, United States 
Area:
Organic Chemistry
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"David Peyton"
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DOI: 10.1021/ja00383a006
DOI: 10.1016/0141-8130(85)90017-0

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J. Thomas Gerig grad student 1983 UC Santa Barbara
 (Rotations about the Carbamoyl CN Bond of Micellar and Non-micellar Alkali N-alkyloxycarbamoyl Sarcosinates: Chemical Modification of Cytochrome C by Immobilization.)
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Publications

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Gunsaru B, Burgess SJ, Morrill W, et al. (2017) Simplified Reversed Chloroquines to Overcome Malaria Resistance to Quinoline-based Drugs. Antimicrobial Agents and Chemotherapy
Pankow JF, Strongin RM, Peyton DH. (2015) Formaldehyde from e-cigarettes--it's not as simple as some suggest. Addiction (Abingdon, England). 110: 1687-8
Wirjanata G, Sebayang BF, Chalfein F, et al. (2015) Contrasting ex vivo efficacy of "reversed chloroquine" compounds in chloroquine resistant Plasmodium falciparum and P. vivax isolates. Antimicrobial Agents and Chemotherapy
Pankow JF, Strongin RM, Peyton DH. (2015) More on hidden formaldehyde in e-cigarette aerosols. The New England Journal of Medicine. 372: 1576-7
Jensen RP, Luo W, Pankow JF, et al. (2015) Hidden formaldehyde in e-cigarette aerosols. The New England Journal of Medicine. 372: 392-4
Alfadhli A, McNett H, Eccles J, et al. (2013) Analysis of small molecule ligands targeting the HIV-1 matrix protein-RNA binding site. The Journal of Biological Chemistry. 288: 666-76
Peyton DH. (2012) Reversed chloroquine molecules as a strategy to overcome resistance in malaria. Current Topics in Medicinal Chemistry. 12: 400-7
Alfadhli A, McNett H, Tsagli S, et al. (2011) HIV-1 matrix protein binding to RNA. Journal of Molecular Biology. 410: 653-66
Burgess SJ, Kelly JX, Shomloo S, et al. (2010) Synthesis, structure-activity relationship, and mode-of-action studies of antimalarial reversed chloroquine compounds. Journal of Medicinal Chemistry. 53: 6477-89
Andrews S, Burgess SJ, Skaalrud D, et al. (2010) Reversal agent and linker variants of reversed chloroquines: activities against Plasmodium falciparum. Journal of Medicinal Chemistry. 53: 916-9
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