Novel silver(I) compounds with 1-adamantanamine
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Abstract
In this work, three novel silver(I) complexes with an almost completely rigid and bulky monodentate ligand, 1-adamantanamine, were synthesized. The aliphatic amine, 1-adamantanamine, is the sole electron donor ligand in these complexes. In addition to spectroscopic characterization, the basic biological activities of the new compounds were investigated and their minimum inhibitory concentrations were determined. The antifungal and antibacterial activities indicate that these compounds could potentially be applied as new therapeutics.
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References
А. Senning, Elsevier's Dictionary of Chemoetymology, Elsevier, Amsterdam, 2006
J. Liu, D. Obando, V. Liao, T. Lifa, R. Codd, Eur. J. Med. Chem. 46 (2011) 1949
А. Boukrinskaia, А. Serbin, О. Bogdan, L. Stotskaya, I. Alymova, Y. Klimochkin, U.S. 5 880 154 (2009)
I. Moiseev, R. Doroshenko, V. Ivanova, Pharm. Chem. J. 10 (1976) 450
H. Stetter, J. Mayer, M. Schwarz, K. Wulf, Chem. Ber. 93 (1960) 226
J. Watts, P. Marvin, U.S. 3 310 469 (1967)
T. Maugh, Science 206 (1979) 1058
L. Sonnberg, The Complete Pill Guide: Everything You Need to Know about Generic and Brand-Name Prescription Drugs, Barnes & Noble Publishing, New York, 2003
T. Blanpied, R. Clarke, J. Johnson, J. Neurosci. 25 (2005) 3312
S. Halder, S.-M. Peng, G.-H. Lee, T. Chatterjee, A. Mukherjee, S. Dutta, U. Sanyal, S. Bhattacharya, New J. Chem. 32 (2008) 105
D. Kovala-Demertzi, M. A. Demertzis, J. R. Miller, C. Papadopoulou, C. Dodorou, G. Filousis, J. Inorg. Biochem. 86 (2001) 555
F. Rochoq, M. Doyon, I. Butler, Inorg. Chem. 32 (1993) 2717
A. Kozubík, A. Vaculová, K. Souček, J. Vondráček, J. Turánek, J. Hofmanová,
Met.-Based Drugs 2008 (2008) 417897
M. Westerhausen, T. Bollwein, A. Pfitzner, T. Nilges, H. Deiseroth, Inorg. Chim. Acta 312 (2001) 239
R. Kaushal, N. Kumar, A. Chaudhary, S. Arora, P. Awasthi, Bioinorg. Chem. Appl. 2014 (2014) 142828
M. Risto, T. T. Takaluoma, T. Bajorek, R. Oilunkaniemi, R. S. Laitinen, T. Chivers, Inorg. Chem. 48 (2009) 6271
W. K. Jung, H. C. Koo, K. W. Kim, S. Shin, S. H. Kim, Y. H. Park, Appl. Environ. Microbiol. 74 (2008) 2171
I. Wiegand, K. Hilpert, R. Hancock, Nat. Protoc. 3 (2008) 163
G. J. Kabo, A. V. Blokhin, M. B. Charapennikau, A. G. Kabo, V. M. Sevruk, Thermochim. Acta 345 (2000) 125
R. H. Boyd, S. N. Sanwal, S. Shary-Tehrany, D. McNally, J. Phys. Chem. 75 (1971) 1264
A. Van Roon, J. R. Parsons, H. A. J. Govers, J. Chromatogr. A 955 (2002) 105
J. Reiser, E. McGregor, J. Jones, R. Enick, G. Holder, Fluid Phase Equilib. 117 (1996) 160
I. Mokbel, K. Ruzicka, V. Majer, V. Ruzicka, M. Ribeiro, J. Jose, M. Zabransky, Fluid Phase Equilib. 169 (2000) 191
W. Z. Florian, Phys. Chem. 61 (1968) 319
A. B. Bazyleva, A. V. Blokhin, G. J. Kabo, M. B. Charapennikau, V. N. Emelyanenko, S. P. Verevkin, V. Diky, J. Phys. Chem. B 115 (2011) 10064
X. Jing, C. Ma, Y. Ohigashi, F. Oliveira, T. Jardetzky, L. Pinto, R. Lamb, Proc. Natl. Acad. Sci. U.S.A. 105 (2008) 10967.