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1
The treatment of experimental bacillary infections of mice with quinoxaline 1:4 di-N-oxide.
Br J Pharmacol Chemother. 1955 Sep;10(3):394-6. doi: 10.1111/j.1476-5381.1955.tb00890.x.
5
Beneficial effect of quinoxaline 1,4-di-N-oxide in radiation injury in mice.
Proc Soc Exp Biol Med. 1957 Dec;96(3):579-82. doi: 10.3181/00379727-96-23546.
6
Quinoxaline and quinoxaline-1,4-di-N-oxides: An emerging class of antimycobacterials.
Arch Pharm (Weinheim). 2018 May;351(5):e1700325. doi: 10.1002/ardp.201700325. Epub 2018 Apr 3.
7
New quinoxaline 1,4-di-N-oxides. Part 1: Hypoxia-selective cytotoxins and anticancer agents derived from quinoxaline 1,4-di-N-oxides.
Bioorg Med Chem. 2006 Oct 15;14(20):6917-23. doi: 10.1016/j.bmc.2006.06.038. Epub 2006 Jul 14.
9
Synthesis, 3D-QSAR analysis and biological evaluation of quinoxaline 1,4-di-N-oxide derivatives as antituberculosis agents.
Bioorg Med Chem Lett. 2016 Aug 15;26(16):4146-53. doi: 10.1016/j.bmcl.2016.01.066. Epub 2016 Jan 22.

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2
Mutagenicity of quindoxin, its metabolites, and two substituted quinoxaline-di-N-oxides.
Antimicrob Agents Chemother. 1981 Sep;20(3):336-43. doi: 10.1128/AAC.20.3.336.
3
Mode of action of quindoxin and substituted quinoxaline-di-N-oxides on Escherichia coli.
Antimicrob Agents Chemother. 1978 May;13(5):770-83. doi: 10.1128/AAC.13.5.770.

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1
Synthetic amoebicides. II. The anti-amoebic action of quinoxaline-1:4-dioxide and some derivatives.
Br J Pharmacol Chemother. 1953 Sep;8(3):286-9. doi: 10.1111/j.1476-5381.1953.tb00796.x.

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