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. Author manuscript; available in PMC: 2018 Jan 1.
Published in final edited form as: SLAS Discov. 2017 Aug 29;23(1):55–64. doi: 10.1177/2472555217728489

Table 3.

Compounds which exhibit a measurable AmpG-specific activity index.

entry ID structure analysis
1 SR-01000076250-2 graphic file with name nihms902999t1.jpg Inorganic dye: poor drug-likeness and poorly-suited for follow-up
2 SR-05000002238-3 graphic file with name nihms902999t2.jpg Patulin: natural product mycotoxin produced by a variety of molds. In ring-opened form it is chemically reactive, forming Schiff bases with biological amines.
3 SR-01000320782-1 graphic file with name nihms902999t3.jpg A synthetic compound: phenolic hydrazones are structure alerts and thus modifications to the structure in probe development would be desirable
4 SR-05000002074-1 graphic file with name nihms902999t4.jpg Natural product Polymyxin B, primarily used for resistant gram-negative infections. It is derived from the bacterium Bacillus polymyxa.
5 SR-01000226538-1 graphic file with name nihms902999t5.jpg A synthetic compound in the aryl guanidine class.
No stability or reactivity concerns.
6 SR-01000115944-1 graphic file with name nihms902999t6.jpg A synthetic compound in the 7-aminomethyl 8-hydroxyquinoline class. These are known as “Betti bases” and may be chemical unstable to retro-Michael addition. More chemically stable analogs would be preferred.
7 SR-01000115950-1 graphic file with name nihms902999t7.jpg A structural isomer also in the 7-aminomethyl 8-hydroxyquinoline class. More chemically stable analogs would be preferred.
8 SR-01000520919-1 graphic file with name nihms902999t8.jpg A synthetic compound in the N-aryl sulfonamide class.
No stability or reactivity concerns.