Summary
Copper(II) complexes of the type [Cu(L)X], where L=tridentate anion of 2-acetylpyridineN 4-diethyl thiosemicarbazone and X=C1 or Br, were screened against seven fungal strains pathogenic to man viz.Aspergillus niger, Aspergillus fumigatus, Candida albicans, Cryptococcus neoformans, Tricophyton rubrum, Epidermophyton foccosum andMicrosporum canis. The greater growth inhibition exhibited by the bromo complex can be explained on the basis of its lower Cu(II)/Cu(I) redox couple and greater covalent bonding. These compounds represent a novel class of metal-based antifungal agents which provide opportunities for a large number of synthetic variations for modulation of the activities.
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References
Collins FM, Klayman DL, Morrison NE (1982) Correlations between structure and antimycobacterial activity in a series of 2-acetylpyridine thiosemicarbazones. J Gen Microb 128:1349–1356
Cooper KE (1964) The theory of antibiotic inhibition zones. In: Kavanagh F (ed) Analytical microbiology. Academic Press, New York, pp 1–86
Eisner V, Eisner U (1970) Derivatives of hydroxylamine and hydrazine. In: Bard AJ, Lund H (eds) Encyclopedia of electrochemistry of the elements. Marcel Dekker, New York, vol XII, pp 219–354
French FA, Blanz EJ Jr (1966) The carcinostatic activity of thiosemicarbazones of formyl heteroaromatic compounds. III Primary correlation. J Med Chem 9:585–589
Hooper M, Purohit MG (1983) The chemotherapy of leprosy. Prog Med Chem 20:l-81
Klayman DL, Bartosevich JF, Griffin TS, Mason CJ, Scoviil JP (1979) 2-Acetylpyridine thiosemicarbazones l. A new class of potential antimalarial agents. J Med Chem 22:855–862
Kumbhar AS, Padhye SB, West DX, Liberta AE (1991) Electrochemical studies of copper(II) 2-acetylpyridineN 4-diaikyl thiosemicarbazones. Relation to their spectral, magnetic and biological properties. Transition Met Chem
Logan JC, Fox MP, Morgan JH, Mokhon AM, Pfau CG (1975) Arenavirus inactivation on contact withN-substitutedβ-thio-semicarbazones and certain cations. J Gen Virol 28:271–283
Moore EC, Zedeck MS, Agrawal KC, Sartorelli AC (1970) Inhibition of ribonucleotide diphosphate reductase by 1-formyl isoquinoline thiosemicarbazone and related compounds. Biochem 9:4492–4498
Parwana HK, Singh G, Talwar P (1985) Antifungal activity of metal complexes of thiosemicarbazones. Inorg Chim Acta 108:87–89
Reevs DS, Bywater MJ, Holt HA (1980) Comparative in vitro activity of Sch 29482 a new penem antibiotic. J Antimicrob Chemother 9:31–36
Scovill JP, Klayman DL, Franchino CF (1982) 2-Acetylpyridine thiosemicarbazones 4. Complexes with transition metals as antimalarial and antileukemic agents. J Med Chem 25:1261–1264
West DX, Carlson CS, Galloway CP, Liberta AE, Daniel CR (1990) Transition metal ion complexes of thiosemicarbazones derived from 2-acetylpyridineN 4-diethyl andN 4-dipropyl thiosemicarbazones and their copper(II) complexes. Transition Met Chem 15:91–95
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Kumbhar, A.S., Padhye, S.B., Saraf, A.P. et al. Novel broad-spectrum metal-based antifungal agents. Biol Metals 4, 141–143 (1991). https://doi.org/10.1007/BF01141304
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DOI: https://doi.org/10.1007/BF01141304