Jonofory (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Jonofory" in Polish language version.

Last modified: 05:47:00, 4 January 2026 (UTC)

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4831doi.org

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archive.ph (Global: 347^th place; Polish: 11^th place)

J. Stefańska, A. Huczyński. Biologiczne właściwości monenzyny A. „Biulety Wydz. Farmacji UMW”. 2, s. 1–12, 2008. (pol.).

doi.org (Global: 2^nd place; Polish: 5^th place)

Berton Pressman. Biological applications of ionophores. „Annu. Rev. Biochem.”. 45, s. 501–530, 1976. DOI: 10.1146/annurev.bi.45.070176.002441. (ang.).
G.F. Gause, M.G. Brazhnikova. Gramicidin S and its use in the treatment of infected wounds. „Nature”. 154, s. 703, 1944. DOI: 10.1038/154703a0. (ang.).
G.F. Gause, M.G. Brazhnikova. Gramicidin S origin and mode of action. „The Lancet”. 244, s. 715–716, 1944. DOI: 10.1016/S0140-6736(00)88377-4. (ang.).
E.J. Prenner i inni. Structure-Activity Relationships of Diastereomeric Lysine Ring Size Analogs of the Antimicrobial Peptide Gramicidin S: Mechanism of action and discrimination between bacterial and animal cell membranes. „J. Biol. Chem.”. 280, s. 2002–2011, 2005. DOI: 10.1074/jbc.M406509200. (ang.).
C. Moore, B.C. Pressman. Mechanism of action of valinomycin on mitochondria. „Biochem. Biophys. Res. Commun.”. 15, s. 562–567, 1964. DOI: 10.1016/0006-291X(64)90505-4. (ang.).
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.).
B.C. Pressman, E.J. Harris, W.S. Jagger, J.H. Johnson. Antibiotic-mediated transport of alkali ions across lipid barriers. „PNAS”. 58, s. 1949–1956, 1967. DOI: 10.1073/pnas.58.5.1949. (ang.).
B.T. Kilbourn, J.D. Dunitz, L.A.R. Pioda, W. Simon. Structure of the K⁺ complex with nonactin, a macrotetrolide antibiotic possessing highly specific K⁺ transport properties. „J. Mol. Biol.”. 30, s. 559–563, 1967. DOI: 10.1016/0022-2836(67)90370-1. (ang.).
M. Pinkerton, L.K. Steinrauf, P. Dawkins. The molecular structure and some transport properties of valinomcin. „Biochem. Biophys. Res. Commun.”. 35, s. 512–518, 1969. DOI: 10.1016/0006-291X(69)90376-3. (ang.).
C.J. Pedersen. The discovery of crown ether (Noble Lecture). „Angew. Chem. Int. Ed. Eng.”. 27, s. 1021–1027, 1988. DOI: 10.1002/anie.198810211. (ang.).
C.J. Pedersen. Cyclic polyethers and their complexes with metal salts. „J. Am. Chem. Soc.”. 89, s. 7017–7036, 1967. DOI: 10.1021/ja01002a035. (ang.).
B.C. Pressman, N.T. DeGuzman. Biological applications of ionophores: theory and practice. „Ann N Y Acad Sci.”. 264, s. 373–386, 1975. DOI: 10.1111/j.1749-6632.1975.tb31497.x. (ang.).
J.W.J.W. Westley J.W.J.W., Polyether antibiotics: Versatile carboxylic acid ionophores produced by Streptomyces, D.D. Perlman (red.), „Advances in Applied Microbiology”, 22, New York, San Francisco, London: Academic Press, 1977, s. 177–223, DOI: 10.1016/S0065-2164(08)70163-1 . ISBN 978-0-12-002622-7.
W.-C. Liu i inni. Ionomycin, a new polyether antibiotic. „J. Antibiot.”. 31, s. 815–819, 1978. DOI: 10.7164/antibiotics.31.815. (ang.).
J. Berger, A.I. Rachlin, W.E. Scott, L.H. Sternbach i inni. The Isolation of Three New Crystalline Antibiotics from Streptomyces. „J. Am. Chem. Soc.”. 73, s. 5295–5298, 1951. DOI: 10.1021/ja01155a084. (ang.).
M. Mitani, T. Yamanishi, Y. Miyazaki. Salinomycin: A new monovalent cation ionophore. „Biochem. Biophys. Res. Commun.”. 66, s. 1231–1236, 1975. DOI: 10.1016/0006-291X(75)90490-8. (ang.).
E. Gäumann, Stephi Roth i inni. Enniatin, ein neues, gegen Mykobakterien wirksames Antibiotikum. „Experientia”. 3, s. 202–203, 1947. DOI: 10.1007/BF02163993. (niem.).
R. Corbaz i inni. Stoffwechselprodukte von Actinomyceten. 3. Mitteilung. Nonactin. „Helv. Chim. Acta”. 38, s. 1445–1448, 1955. DOI: 10.1002/hlca.19550380617. (niem.).
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.).
lariat ethers, [w:] Compendium of Chemical Terminology, International Union of Pure and Applied Chemistry, wer. 5.0.0, 2025, DOI: 10.1351/goldbook.L03458 (ang.).
A. Huczyński, P. Przybylski, B. Brzezinski, F. Bartl. Spectroscopic and semiempirical studies of a proton channel formed by the methyl ester of Monensin A. „J. Phys. Chem. B”. 110, s. 15615–15623, 2006. DOI: 10.1021/jp062160o. (ang.).
D.C. Tosteson, B.F. Gisin. Ion transport mediated by the valinomycin analogue cyclo(LLac- L-Val-D-Pro-D-Val)3 in lipid bilayer membranes. „J. Gen. Physiol.”. 77, s. 387–417, 1981. DOI: 10.1085/jgp.77.4.387. PMID: 7241088. PMCID: PMC2215419. (ang.).
Y. Itoh, M.J. Law, L. Sokoloff. Effects of the Na⁺/H⁺ exchanger monensin on intracellular pH in astroglia. „Brain Research”. 882, s. 226–229, 2000. DOI: 10.1016/S0006-8993(00)02822-5. (ang.).
H. Tsukube i inni. Biomimetic transport of unusual metal cations and amino acid ester salts mediated by monensin and lasalocid A. „J. Chem. Soc., Chem. Commun.”, s. 448–449, 1986. DOI: 10.1039/C39860000448. (ang.).
H. Tsukube i inni. Biomimetic membrane transport: Interesting ionophores functions of naturally occurring polyether antibiotics toward unusual metal cations and amino did ester salts. „Inorg. Chem.”. 33, s. 2984–2987, 1994. DOI: 10.1021/ic00091a043. (ang.).
A. Huczyński, J. Jaczkak, D. Łowicki, B. Brzezinski. Monensin A acid complexes as a model of electrogenic transport of sodium cation. „Biochim. Biophys. Acta”. 1818, s. 2108–2119, 2012. DOI: 10.1016/j.bbamem.2012.04.017.
M. Inabayashi, S. Miyauchi, N. Kamo, T. Jin. Conductance change in phospholipid bilayer membrane by an electroneutral ionophore, monensin. „Biochemistry”. 34, s. 3455–3460, 1995. DOI: 10.1021/bi00010a038. (ang.).
A. Huczyński, J. Stefańska i inni. Synthesis and antimicrobial properties of Monensin A esters. „Bioorg. Med. Chem. Lett.”. 18, s. 2585–2589, 2008. DOI: 10.1016/j.bmcl.2008.03.038. (ang.).
Satake M.,Murata M.,Yasumoto T.. The structure of CTX3C, a ciguatoxin congener isolated from cultured Gambierdiscus toxicus. „Tetrahedron Lett.”. 34, s. 1975–1978, 1993. DOI: 10.1016/S0040-4039(00)91978-6. (ang.).
18-Crown-6. W: C.L. Liotta, J. Berknerin: Encyclopedia of Reagents for Organic Synthesis. L. Paquette (red.). New York: J. Wiley & Sons, 2001. DOI: 10.1002/047084289X.rc261. ISBN 978-0-470-84289-8.

ip.com (Global: low place; Polish: low place)

C.J.C.J. Pedersen C.J.C.J., Chelated compounds of vanadium and substituted phenols US-Patent 3361778 Du Pont, United States Patent Office, 1968 (ang.).

jbc.org (Global: 6,339^th place; Polish: 7,428^th place)

E.J. Prenner i inni. Structure-Activity Relationships of Diastereomeric Lysine Ring Size Analogs of the Antimicrobial Peptide Gramicidin S: Mechanism of action and discrimination between bacterial and animal cell membranes. „J. Biol. Chem.”. 280, s. 2002–2011, 2005. DOI: 10.1074/jbc.M406509200. (ang.).

jst.go.jp (Global: 1,248^th place; Polish: 3,779^th place)

jstage.jst.go.jp

W.-C. Liu i inni. Ionomycin, a new polyether antibiotic. „J. Antibiot.”. 31, s. 815–819, 1978. DOI: 10.7164/antibiotics.31.815. (ang.).

mendeley.com (Global: low place; Polish: low place)

C.J. Pedersen. The discovery of crown ether (Noble Lecture). „Angew. Chem. Int. Ed. Eng.”. 27, s. 1021–1027, 1988. DOI: 10.1002/anie.198810211. (ang.).

nih.gov (Global: 5^th place; Polish: 7^th place)

ncbi.nlm.nih.gov

F. Sanger. The free amino group of gramicidin S. „Biochem. J.”. 40, s. 261–262, 1946. PMCID: PMC1258332. (ang.).
R. Consden, A.H. Gordon, A.J.P. Martin, R.L.M. Synge. Gramicidin S: the sequence of the amino-acid residues. „Biochem. J.”. 41, s. 596–602, 1947. PMCID: PMC1258544. (ang.).
M.E. Haney Jr., M.M. Hoehn. Monensin, a new biologically active compound. I. Discovery and isolation. „Antimicrob. Agents Chemother.”. 7, s. 349–352, 1967. PMID: 5596158. (ang.).
R.L. Harned i inni. Nigericin, a new crystalline antibiotic from an unidentified streptomyces. „Antibiot. Chemother.”. 1, s. 594, 1951. PMID: 24541690. (ang.).
F.R. Champlin, E.A. Grula. Noninvolvement of Beauvericin in the entomopathogenicity of Beauveria bassiana. „Appl. Environ. Microbiol.”. 37, s. 1122–1126, 1979. PMID: 573587. PMCID: PMC243365. (ang.).
A. Logrieco, A. Moretti, G. Castella. Beauvericin production by Fusarium species. „Appl. Environ. Microbiol.”. 64, s. 3084–3088, 1998. PMID: 9687479. PMCID: PMC106821. (ang.).
D.W. Urry. The Gramicidin A Transmembrane Channel: A Proposed _π(L,D) Helix. „PNAS”. 68, s. 672–676, 1971. PMID: 5276779. PMCID: PMC389014. (ang.).
D.C. Tosteson, B.F. Gisin. Ion transport mediated by the valinomycin analogue cyclo(LLac- L-Val-D-Pro-D-Val)3 in lipid bilayer membranes. „J. Gen. Physiol.”. 77, s. 387–417, 1981. DOI: 10.1085/jgp.77.4.387. PMID: 7241088. PMCID: PMC2215419. (ang.).

nobelprize.org (Global: 265^th place; Polish: 173^rd place)

Charles J. Pedersen: The discovery of crown ethers Lobel lecture. 1987-12-08. [dostęp 2019-01-14]. (ang.).

patents.google.com (Global: 1,154^th place; Polish: 2,299^th place)

D.G.D.G. Stewart D.G.D.G., D.Y.D.Y. Waddan D.Y.D.Y., E.T.E.T. Borrows E.T.E.T., Improvements in and relating to the production of alkylene oxide polymers, United Kingdom Patent GB785229, 23 października 1957 .
R.M.R.M. Gale R.M.R.M., C.E.C.E. Higgins C.E.C.E., M.M.M.M. Hoehn M.M.M.M., Antibiotic A23187 and Process for preparation thereof, US Patent 3923823, 1975 .

pnas.org (Global: 1,411^th place; Polish: 1,370^th place)

B.C. Pressman. Inducted active transport of ions in mitochondria. „PNAS”. 3, s. 1076–1083, 1965. (ang.).
B.C. Pressman, E.J. Harris, W.S. Jagger, J.H. Johnson. Antibiotic-mediated transport of alkali ions across lipid barriers. „PNAS”. 58, s. 1949–1956, 1967. DOI: 10.1073/pnas.58.5.1949. (ang.).
D.W. Urry. The Gramicidin A Transmembrane Channel: A Proposed _π(L,D) Helix. „PNAS”. 68, s. 672–676, 1971. PMID: 5276779. PMCID: PMC389014. (ang.).

rupress.org (Global: low place; Polish: low place)

L. Ernstern, G. Schatz. Mitochondria: A Historical Review. „J. Cell Biol.”. 91, s. 227–255, 1981. (ang.).

wbc.poznan.pl (Global: 2,699^th place; Polish: 91^st place)

G. Schroeder, B. Gierczyk: 1. Syntetyczne receptory jonowe – jonofory. W: Syntetyczne receptory jonowe. Poznań: Betagraf P.U.H., 2005. ISBN 83-89936-05-4. [dostęp 2014-05-25]. Wersja on-line: Wielkopolska Biblioteka Cyfrowa.
G. Schroeder, B. Łęska: Rozpuszczalniki podandowe. W: Kompleksy typu gość-gospodarz. Poznań: Betagraf P.U.H., 2003, s. 18–39. ISBN 83-918771-1-6. [dostęp 2014-05-25]. Wersja on-line: Wielkopolska Biblioteka Cyfrowa.

web.archive.org (Global: 1^st place; Polish: 1^st place)

D.C. Tosteson, B.F. Gisin. Ion transport mediated by the valinomycin analogue cyclo(LLac- L-Val-D-Pro-D-Val)3 in lipid bilayer membranes. „J. Gen. Physiol.”. 77, s. 387–417, 1981. DOI: 10.1085/jgp.77.4.387. PMID: 7241088. PMCID: PMC2215419. (ang.).
R. Narayan, G.T. Tsao. Application of crown ethers as phase transfer catalysts in the electron transfer reactions of coal. „Conference: 186. national meeting of the American Chemical Society, Washington, DC, USA, 28 Aug 1983”. s. 261–267. (ang.).

Jonofory (Polish Wikipedia)

archive.ph (Global: 347th place; Polish: 11th place)

doi.org (Global: 2nd place; Polish: 5th place)

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jbc.org (Global: 6,339th place; Polish: 7,428th place)

jst.go.jp (Global: 1,248th place; Polish: 3,779th place)

jstage.jst.go.jp

mendeley.com (Global: low place; Polish: low place)

nih.gov (Global: 5th place; Polish: 7th place)

ncbi.nlm.nih.gov

nobelprize.org (Global: 265th place; Polish: 173rd place)

patents.google.com (Global: 1,154th place; Polish: 2,299th place)

pnas.org (Global: 1,411th place; Polish: 1,370th place)

rupress.org (Global: low place; Polish: low place)

wbc.poznan.pl (Global: 2,699th place; Polish: 91st place)

web.archive.org (Global: 1st place; Polish: 1st place)

archive.ph (Global: 347^th place; Polish: 11^th place)

doi.org (Global: 2^nd place; Polish: 5^th place)

jbc.org (Global: 6,339^th place; Polish: 7,428^th place)

jst.go.jp (Global: 1,248^th place; Polish: 3,779^th place)

nih.gov (Global: 5^th place; Polish: 7^th place)

nobelprize.org (Global: 265^th place; Polish: 173^rd place)

patents.google.com (Global: 1,154^th place; Polish: 2,299^th place)

pnas.org (Global: 1,411^th place; Polish: 1,370^th place)

wbc.poznan.pl (Global: 2,699^th place; Polish: 91^st place)

web.archive.org (Global: 1^st place; Polish: 1^st place)