Exploration of the antibiotic potentiating activity of indolglyoxylpolyamines
- Eur J Med Chem. 2019 Dec 1:183:111708. doi: 10.1016/j.ejmech.2019.111708.
- 1. School of Chemical Sciences, The University of Auckland, Private Bag 92019, Auckland, 1142, New Zealand.
- 2. School of Pharmacy, The University of Auckland, Private Bag 92019, Auckland, 1142, New Zealand.
- 3. Laboratoire Molécules de Communication et Adaptation des Micro-organismes, UMR 7245 CNRS, Muséum National d'Histoire Naturelle, 57 Rue Cuvier (C.P. 54), 75005, Paris, France.
- 4. Aix Marseille Univ, INSERM, SSA, MCT, Faculté de Pharmacie, 27 bd Jean Moulin, 13385, Marseille, France.
- 5. YELEN, 10 bd Tempête, 13820, Ensues la Redonne, France.
- 6. School of Chemical Sciences, The University of Auckland, Private Bag 92019, Auckland, 1142, New Zealand. Electronic address: [email protected].
A series of substituted di-indolglyoxylamido-spermine analogues were prepared and evaluated for intrinsic antimicrobial properties and the ability to enhance Antibiotic action. As a compound class, intrinsic activity was typically observed towards Gram-positive bacteria and the fungus Cryptococcus neoformans, with notable exceptions being the 5-bromo- and 6-chloro-indole analogues which also exhibited modest activity (MIC 34-50 μM) towards the Gram-negative bacteria Escherichia coli and Klebsiella pneumoniae. Several analogues enhanced the activity of doxycycline towards the Gram-negative bacteria Pseudomonas aeruginosa, E. coli, K. pneumoniae and Acinetobacter baumannii. Of particular note was the identification of five Antibiotic enhancing analogues (5-Br, 7-F, 5-Me, 7-Me, 7-OMe) which also exhibited low to no cytotoxicity and red blood cell haemolytic properties. The mechanisms of action of the 5-Br and 7-F analogues were attributed to the ability to disrupt the integrity of, and depolarize, Bacterial membranes.