Structural requirements of salicylanilides for uncoupling activity in mitochondria: quantitative analysis of structure-uncoupling relationships
- PMID: 3196713
- DOI: 10.1016/0005-2728(88)90027-8
Structural requirements of salicylanilides for uncoupling activity in mitochondria: quantitative analysis of structure-uncoupling relationships
Abstract
The uncoupling activities of more than 20 salicylanilides were measured in rat liver mitochondria. The activities, expressed as the minimum concentrations required for full release of state-4 respiration, ranged over three orders of magnitude. The acid dissociation constant, pKA, and the partition coefficient between octanol and water (Poct) of some of the salicylanilides were determined. These two parameters were found to be well expressed in terms of the Hammett constant, sigma, and the hydrophobic substituent coefficient, II, respectively. The pKA and log Poct values of all the salicylanilides were predicted according to these relationships. Furthermore, the capacity factor, k', on high-performance liquid chromatography was determined on glyceryl-coated-controlled pore glass (gly-CPG). Values of log k' correlated well with those of log Poct. The uncoupling activities of the salicylanilides were analyzed in terms of these three parameters. Both hydrophobic and electron-withdrawing properties were found to be essential for induction of potent uncoupling activity. The correlations using log k' were better than those using log Poct.
Similar articles
-
Structure-activity relationships of three groups of uncouplers of oxidative phosphorylation: salicylanilides, 2-trifluoromethylbenzimidazoles, and phenols.J Med Chem. 1973 Jul;16(7):791-6. doi: 10.1021/jm00265a011. J Med Chem. 1973. PMID: 4269408 No abstract available.
-
Closantel, a new antiparasitic hydrogen ionophore [proceedings].Arch Int Physiol Biochim. 1979 Oct;87(4):851-3. Arch Int Physiol Biochim. 1979. PMID: 93944 No abstract available.
-
Steric and electronic effects on the uncoupling activity of substituted 3,5 dichlorosalicylanilides.FEBS Lett. 1975 Jan 1;49(3):338-41. doi: 10.1016/0014-5793(75)80780-0. FEBS Lett. 1975. PMID: 1109918 No abstract available.
-
[Uncouplers (author's transl)].Tanpakushitsu Kakusan Koso. 1973 Oct;18(10):911-9. Tanpakushitsu Kakusan Koso. 1973. PMID: 4271985 Review. Japanese. No abstract available.
-
Salicylanilides and Their Anticancer Properties.Int J Mol Sci. 2023 Jan 15;24(2):1728. doi: 10.3390/ijms24021728. Int J Mol Sci. 2023. PMID: 36675241 Free PMC article. Review.
Cited by
-
Insight into antistaphylococcal effect of chlorinated 1-hydroxynaphthalene-2-carboxanilides.ADMET DMPK. 2025 Mar 26;13(2):2684. doi: 10.5599/admet.2684. eCollection 2025. ADMET DMPK. 2025. PMID: 40314001 Free PMC article.
-
Structure-activity relationships of antitubercular salicylanilides consistent with disruption of the proton gradient via proton shuttling.Bioorg Med Chem. 2013 Jan 1;21(1):114-26. doi: 10.1016/j.bmc.2012.10.056. Epub 2012 Nov 15. Bioorg Med Chem. 2013. PMID: 23211970 Free PMC article.
-
Antimycobacterial activity of salicylanilide benzenesulfonates.Molecules. 2012 Jan 5;17(1):492-503. doi: 10.3390/molecules17010492. Molecules. 2012. PMID: 22222908 Free PMC article.
-
Uncouplers of oxidative phosphorylation.Environ Health Perspect. 1990 Jul;87:213-8. doi: 10.1289/ehp.9087213. Environ Health Perspect. 1990. PMID: 2176586 Free PMC article. Review.
-
Structural investigations on the mitochondrial uncouplers niclosamide and FCCP.FEBS Open Bio. 2024 Jul;14(7):1057-1071. doi: 10.1002/2211-5463.13817. Epub 2024 May 15. FEBS Open Bio. 2024. PMID: 38750619 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources