H. Brockmann, G. Schmidt-Kastner. Valinomycin I, XXVII. Mitteil. über antibiotica aus actinomyceten. „Chem. Ber.”. 88, s. 57-61, 1955. DOI: 10.1002/cber.19550880111. (niem.).
M. Hofert, B.C. Pressman. Stimulation of oxidative phosphorylation in mitochondria by potassium in the presence of valinomycin. „Biochemistry”. 5, s. 3919-3925, 1965. DOI: 10.1021/bi00876a025. (ang.).
E. Ogata, H. Rasmussen. Valinomycin and mitochondrial ion transport. „Biochemistry”. 5, s. 57-66, 1966. DOI: 10.1021/bi00865a009. (ang.).
M.M. Shemyakin i inni. The structure-antimicrobial relation for valinomycin depsipeptides. „Experientia”. 21, s. 548-552, 1965. DOI: 10.1007/BF02138991. (ang.).
G.D. Smith, W.L. Duax, i inni. Crystal and molecular structure of the triclinic and monoclinic forms of valinomycin, C54H90N6O18. „J. Am. Chem. Soc.”. 97, s. 7242–7247, 1975. DOI: 10.1021/ja00858a008. (ang.).
I.L. Karle. Conformation of valinomycin in a triclinic crystal form. „J. Am. Chem. Soc.”. 97, s. 4379–4386, 1975. DOI: 10.1021/ja00848a041. (ang.).
L.K. Steinrauf, J.A. Hamilton, M.N. Sabesan. Crystal structure of valinomycin sodium picrate: Anion effects on valinomycin – cation complexes. „J. Am. Chem. Soc.”. 104, s. 4085-4091, 1982. DOI: 10.1021/ja00379a008. (ang.).
T.R. Forester, W. Smith, J.H.R. Clarke. Antibiotic activity of valinomycin. Molecular dynamics simulations involving the water/membrane interface. „J. Chem. Soc., Faraday Trans.”. 93, s. 613-619, 1997. DOI: 10.1039/A606452C. (ang.).
M.C. Rose, R.W. Henkens. Stability of sodium and potassium complexes of valinomycin. „BBA”. 372, s. 426-435, 1974. DOI: 10.1016/0304-4165(74)90204-9. (ang.).
M. Daňková, E. Makrlík, P. Vaňura. Stability of the valinomycin-rubidium complex in water saturated nitrobenzene. „J. Radioanal. Nucl. Chem.”. 221, s. 251-253, 1997. DOI: 10.1007/BF02035281. (ang.).
E. Makrlík, P. Vaňura. Stability of complex of Cs+ with valinomycin in nitrobenzene saturated with water. „J. Radioanal. Nucl. Chem.”. 214, s. 339-346, 1996. DOI: 10.1007/BF02164376. (ang.).
J. Kříž, J. Dybal, E. Makrlík. Valinomycin–proton interaction in low-polarity media. „Biopolymers”. 82, s. 536–548, 2006. DOI: 10.1002/bip.20506. (ang.).
V.V. Teplova, i inni. The higher toxicity of cereulide relative to valinomycin is due to its higher affinity for potassium at physiological plasma concentration. „Toxicol. Appl. Pharmacol”. 210, s. 39-46, 2006. DOI: 10.1016/j.taap.2005.06.012. (ang.).
Y.-Q. Cheng. Deciphering the biosynthetic codes for the potent anti-SARS-CoV cyclodepsipeptide valinomycin in Streptomyces tsusimaensis ATCC 15141. „ChemBioChem”. 7, s. 471-477, 2006. DOI: 10.1002/cbic.200500425. (ang.).
C. Gabrielli, i inni. Investigation of ion-selective electrodes with neutral ionophores and ionic sites by EIS. II. Application to K+ detection. „J. Electroanal. Chem.”. 570, s. 291-304, 2004. DOI: 10.1016/j.jelechem.2004.04.007. (ang.).
R. Kanne. Isolation and characterization of a potassium specific ionophore from Streptococcus faecalis. „Z. Naturforschung C”. 32, s. 926-928, 1977. ISSN0341-0382. (ang.).PubMed
R. Kanne. Isolation and characterization of a potassium specific ionophore from Streptococcus faecalis. „Z. Naturforschung C”. 32, s. 926-928, 1977. ISSN0341-0382. (ang.).PubMed
M.A. Kroteń, M. Bartoszewicz, I. Święcicka. Cereulide and valinomycin, two important natural dodecadepsipeptides with ionophoretic atcivities. „Pol. J. Microbiol.”. 59, s. 3-10, 2010. ISSN1733-1331. (ang.).