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. Author manuscript; available in PMC: 2021 Jun 14.
Published in final edited form as: Prog Biophys Mol Biol. 2020 Aug 30;158:33–46. doi: 10.1016/j.pbiomolbio.2020.08.005

Table 1.

Exogenous sources of ICLs, their preferential DNA targets, and representative chemical structures for each.

ICL Agent Target Sequence Structurea

Mitomycin C 5′-CG graphic file with name nihms-1710277-t0001.jpg
Pyrrolobenzodiazepines Purine-GATC-pyrimidine graphic file with name nihms-1710277-t0002.jpg
Colibactin 5′-AATTT and 5′-ATTTT graphic file with name nihms-1710277-t0003.jpg
Psoralens 5′-TA graphic file with name nihms-1710277-t0004.jpg
Pyrrolizidine alkaloids N2 guanine in 5′-CG-3′ graphic file with name nihms-1710277-t0005.jpg
Nitrogen mustards 5′-GNC graphic file with name nihms-1710277-t0006.jpg
Chloroethylnitrosoureas O6- and N7 positions of guanine graphic file with name nihms-1710277-t0007.jpg
Cisplatin 5′-GC graphic file with name nihms-1710277-t0008.jpg
Diepoxybutane 5′-GNC graphic file with name nihms-1710277-t0009.jpg
Dianhydrogalactitol N7 guanine graphic file with name nihms-1710277-t0010.jpg
a

Many of these structures can vary by the presence of a number of different possible–R groups. For the sake of brevity, the simplest molecular scaffolds are shown.