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Volumn 62, Issue 1, 2009, Pages 27-35

Micafungin: A sulfated echinocandin

Author keywords

1,3 glucan synthase; Antifungal; Echinocandin; FK463; Micafungin

Indexed keywords

1,3 BETA GLUCAN SYNTHASE; ACULEACIN AR; AMPHOTERICIN B; ANTIFUNGAL AGENT; CILOFUNGIN; ECHINOCANDIN; ECHINOCANDIN B; FLUCONAZOLE; FR 131535; FR 133302; FR 179642; FR 190293; FR 209602; FR 209603; FR 209604; FR 220897; FR 220899; FR 227673; FR 901376; FR 901379; FR 901381; FR 901382; MICAFUNGIN; MULUNDOCANDIN; PNEUMOCANDIN BO; SULFATE; UNCLASSIFIED DRUG; WATER;

EID: 62449290386     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.1038/ja.2008.3     Document Type: Review
Times cited : (53)

References (46)
  • 1
    • 0036916341 scopus 로고    scopus 로고
    • Recent trends in the epidemiology of invasive mycoses
    • Clark, T. A. & Hajjeh, R. A. Recent trends in the epidemiology of invasive mycoses. Curr. Opin. Infect. Dis. 15, 569-574 (2002).
    • (2002) Curr. Opin. Infect. Dis , vol.15 , pp. 569-574
    • Clark, T.A.1    Hajjeh, R.A.2
  • 3
    • 0015360661 scopus 로고
    • Nephrotoxicity of amphotericin B, with emphasis on changes in tubular function
    • Burges, J. L. & Birchall, R. Nephrotoxicity of amphotericin B, with emphasis on changes in tubular function. Am. J. Med. 53, 77-84 (1972).
    • (1972) Am. J. Med , vol.53 , pp. 77-84
    • Burges, J.L.1    Birchall, R.2
  • 4
    • 0030828120 scopus 로고    scopus 로고
    • Clinically significant azole cross-resistance in Candida isolates from HIV-positive patients with oral candidiasis
    • Carledge, J. D., Midgley, J. & Gazzard, B. G. Clinically significant azole cross-resistance in Candida isolates from HIV-positive patients with oral candidiasis. AIDS 11, 1839-1844 (1997).
    • (1997) AIDS , vol.11 , pp. 1839-1844
    • Carledge, J.D.1    Midgley, J.2    Gazzard, B.G.3
  • 5
    • 33745234214 scopus 로고    scopus 로고
    • Newer triazole antifungal agents: Pharmacology, spectrum, clinical efficacy and limitations
    • Aperis, G. & Mylonakis, E. Newer triazole antifungal agents: pharmacology, spectrum, clinical efficacy and limitations. Expert Opin. Investig. Drugs 15, 579-602 (2006).
    • (2006) Expert Opin. Investig. Drugs , vol.15 , pp. 579-602
    • Aperis, G.1    Mylonakis, E.2
  • 6
    • 0016338169 scopus 로고
    • Echinocandin Bein neuartiges polipeptide-antibiotikum aus Aspergillus nidulans var.echinatus: Isolierung und Bausteine.
    • Nyfeler, R. & Keller-Schierlein, W. Echinocandin Bein neuartiges polipeptide-antibiotikum aus Aspergillus nidulans var.echinatus: Isolierung und Bausteine. Helvet. Chim. Acta. 57, 2459-2477 (1974).
    • (1974) Helvet. Chim. Acta , vol.57 , pp. 2459-2477
    • Nyfeler, R.1    Keller-Schierlein, W.2
  • 7
    • 0024502955 scopus 로고    scopus 로고
    • Schwartz, R. E., Giacobbe, R. A., Boand, J. A. & Monaghan, R. L. L-671,329, a new antifungal agent. I. Fermentation and isolation. J. Antibiot. 42, 163-167 (1989).
    • Schwartz, R. E., Giacobbe, R. A., Boand, J. A. & Monaghan, R. L. L-671,329, a new antifungal agent. I. Fermentation and isolation. J. Antibiot. 42, 163-167 (1989).
  • 8
    • 0028148980 scopus 로고    scopus 로고
    • Iwamoto,T. et al. WF11899A, B, and C, novel antifungal lipopeptides. I. Taxonomy, fermentation, isolation and physico-chemical properties. J. Antibiot. 47, 1084-1091 (1994).
    • Iwamoto,T. et al. WF11899A, B, and C, novel antifungal lipopeptides. I. Taxonomy, fermentation, isolation and physico-chemical properties. J. Antibiot. 47, 1084-1091 (1994).
  • 9
    • 0024157407 scopus 로고
    • The synthesis and evaluation of LY121019: A member of a series of semi-synthetic analogs of the antifungal lipopeptide echinocandin B
    • Debono, M. et al. The synthesis and evaluation of LY121019: A member of a series of semi-synthetic analogs of the antifungal lipopeptide echinocandin B. Ann. NY Acad. Sci. 544, 152-167 (1988).
    • (1988) Ann. NY Acad. Sci , vol.544 , pp. 152-167
    • Debono, M.1
  • 10
    • 0029154315 scopus 로고
    • Semisynthetic chemical modification of the antifungal lipopeptide echinocandin B (ECB): Structure-activity studies of the lipophilic and geometric parameters of polyarylated acyl analogs of ECB
    • Debono, M. et al. Semisynthetic chemical modification of the antifungal lipopeptide echinocandin B (ECB): structure-activity studies of the lipophilic and geometric parameters of polyarylated acyl analogs of ECB. J. Med. Chem. 38, 3271-3281 (1995).
    • (1995) J. Med. Chem , vol.38 , pp. 3271-3281
    • Debono, M.1
  • 11
    • 17044455920 scopus 로고    scopus 로고
    • In vitro preclinical evaluation studies with the echinocandin antifungal MK-0991 (L-743,872)
    • Bartizal, K. et al. In vitro preclinical evaluation studies with the echinocandin antifungal MK-0991 (L-743,872). Antimicrob. Agents Chemother. 41, 2326-2332 (1997).
    • (1997) Antimicrob. Agents Chemother , vol.41 , pp. 2326-2332
    • Bartizal, K.1
  • 12
    • 0035992113 scopus 로고    scopus 로고
    • Denning, D. W. Echinocandins: a new class of antifungal. J. Antimicrob. Chemother. 49, 889-891 (2002).
    • Denning, D. W. Echinocandins: a new class of antifungal. J. Antimicrob. Chemother. 49, 889-891 (2002).
  • 13
    • 34248386937 scopus 로고    scopus 로고
    • Role of micafungin in the antifungal armamentarium
    • Ikeda, F. et al. Role of micafungin in the antifungal armamentarium. Curr. Med. Chem. 14, 1263-1275 (2007).
    • (2007) Curr. Med. Chem , vol.14 , pp. 1263-1275
    • Ikeda, F.1
  • 16
    • 34247632542 scopus 로고    scopus 로고
    • Discovery of micafungin (FK453): A novel antifungal drug derived from a naural product lead
    • Fujie, A. Discovery of micafungin (FK453): a novel antifungal drug derived from a naural product lead. Pure Appl. Chem. 79, 603-614 (2007).
    • (2007) Pure Appl. Chem , vol.79 , pp. 603-614
    • Fujie, A.1
  • 17
    • 0020060160 scopus 로고
    • Studies on the mechanism of antifungal action of aculeacin A
    • Yamaguchi, H., Hiratani, T., Iwata, K. & Yamamoto, Y. Studies on the mechanism of antifungal action of aculeacin A. J. Antibiot. 35, 210-219 (1982).
    • (1982) J. Antibiot , vol.35 , pp. 210-219
    • Yamaguchi, H.1    Hiratani, T.2    Iwata, K.3    Yamamoto, Y.4
  • 18
    • 0024519380 scopus 로고
    • Synthesis of new analogs of echinocandin B by enzymatic deacylation and chemical reacylation of the echinocandin B peptide: Synthesis of the antifungal agent cilofungin (LY121019)
    • Debono, M. et al. Synthesis of new analogs of echinocandin B by enzymatic deacylation and chemical reacylation of the echinocandin B peptide: synthesis of the antifungal agent cilofungin (LY121019). J. Antibiot. 42, 389-397 (1989).
    • (1989) J. Antibiot , vol.42 , pp. 389-397
    • Debono, M.1
  • 19
    • 0027103059 scopus 로고
    • Pneumocandins fromZalerion arboricola. IV. Biological evaluation of natural and semisynthetic pneumocandins for activity against Pneumocystis carinii and Candida species
    • Schmatz, D. M. et al. Pneumocandins fromZalerion arboricola. IV. Biological evaluation of natural and semisynthetic pneumocandins for activity against Pneumocystis carinii and Candida species. J. Antibiot. 45, 1886-1891 (1992).
    • (1992) J. Antibiot , vol.45 , pp. 1886-1891
    • Schmatz, D.M.1
  • 20
    • 0028148187 scopus 로고    scopus 로고
    • Iwamoto, T., Fujie, A., Nitta, K., Hashimoto, S., Okuhara, M. & Kohsaka, M. WF11899A, B and C, novel antifungal lipopeptides. II. Biological properties. J. Antibiot. 47, 1092-1097 (1994).
    • Iwamoto, T., Fujie, A., Nitta, K., Hashimoto, S., Okuhara, M. & Kohsaka, M. WF11899A, B and C, novel antifungal lipopeptides. II. Biological properties. J. Antibiot. 47, 1092-1097 (1994).
  • 22
    • 0024603393 scopus 로고
    • Deacylation of echinocandin B by Actinoplanes utahensis
    • Boeck, L. D., Fukuda, D. S., Abbott, B. J. & Debono, M. Deacylation of echinocandin B by Actinoplanes utahensis. J. Antibiot. 42, 382-388 (1989).
    • (1989) J. Antibiot , vol.42 , pp. 382-388
    • Boeck, L.D.1    Fukuda, D.S.2    Abbott, B.J.3    Debono, M.4
  • 23
    • 0035847682 scopus 로고    scopus 로고
    • FR131535, a novel water-soluble echinocandin-like lipopeptide: Synthesis and biological properties
    • Fujie, A. et al. FR131535, a novel water-soluble echinocandin-like lipopeptide: synthesis and biological properties. Bioorg. Med. Chem. Lett. 11, 399-402 (2001).
    • (2001) Bioorg. Med. Chem. Lett , vol.11 , pp. 399-402
    • Fujie, A.1
  • 24
    • 42949150245 scopus 로고    scopus 로고
    • Novel echinocandin antifungals. Part 2: Optimization of the side chain of the natural product FR901379
    • Tomishima, M., Ohki, H., Yamada, A., Maki, K. & Ikeda, F. Novel echinocandin antifungals. Part 2: Optimization of the side chain of the natural product FR901379. Bioorg. Med. Chem. Lett. 18, 2886-2890 (2008).
    • (2008) Bioorg. Med. Chem. Lett , vol.18 , pp. 2886-2890
    • Tomishima, M.1    Ohki, H.2    Yamada, A.3    Maki, K.4    Ikeda, F.5
  • 25
    • 38949209844 scopus 로고    scopus 로고
    • Novel echinocandin antifungals. Part 1: Novel side-chain analogs of the natural product FR901379
    • Tomishima, M., Ohki, H., Yamada, A., Maki, K. & Ikeda, F. Novel echinocandin antifungals. Part 1: Novel side-chain analogs of the natural product FR901379. Bioorg. Med. Chem. Lett. 18, 1474-1477 (2008).
    • (2008) Bioorg. Med. Chem. Lett , vol.18 , pp. 1474-1477
    • Tomishima, M.1    Ohki, H.2    Yamada, A.3    Maki, K.4    Ikeda, F.5
  • 26
    • 0032810033 scopus 로고    scopus 로고
    • FK463, a novel water-soluble echinocandin lipopeptide: Synthesis and antifungal activity
    • Tomishima, M. et al. FK463, a novel water-soluble echinocandin lipopeptide: synthesis and antifungal activity. J. Antibiot. 52, 674-676 (1999).
    • (1999) J. Antibiot , vol.52 , pp. 674-676
    • Tomishima, M.1
  • 27
    • 54749150650 scopus 로고    scopus 로고
    • Use of a serum-based antifungal susceptibility assay to predict the in vivo efficacy of novel echinocandin compounds
    • Maki, K. et al. Use of a serum-based antifungal susceptibility assay to predict the in vivo efficacy of novel echinocandin compounds. Microbiol. Immunol. 52, 383-391 (2008).
    • (2008) Microbiol. Immunol , vol.52 , pp. 383-391
    • Maki, K.1
  • 28
    • 0141863188 scopus 로고    scopus 로고
    • Echinocandin antifungal drugs
    • Denning, D. W. Echinocandin antifungal drugs. Lancet 362, 1142-1151 (2003).
    • (2003) Lancet , vol.362 , pp. 1142-1151
    • Denning, D.W.1
  • 29
    • 0030943354 scopus 로고    scopus 로고
    • Lipopeptide inhibitors of fungal glucan synthase
    • Kurtz, M. B. & Douglas, C. M. Lipopeptide inhibitors of fungal glucan synthase. J. Med. Vet. Mycol. 35, 79-86 (1997).
    • (1997) J. Med. Vet. Mycol , vol.35 , pp. 79-86
    • Kurtz, M.B.1    Douglas, C.M.2
  • 30
    • 0036209847 scopus 로고    scopus 로고
    • Antifungal mechanism of FK463 against Candida albicans and Aspergillus fumigatus
    • Hatano, K., Morishita, Y., Nakai, T. & Ikeda, F. Antifungal mechanism of FK463 against Candida albicans and Aspergillus fumigatus. J. Antibiot. 55, 219-222 (2002).
    • (2002) J. Antibiot , vol.55 , pp. 219-222
    • Hatano, K.1    Morishita, Y.2    Nakai, T.3    Ikeda, F.4
  • 31
    • 0029892037 scopus 로고    scopus 로고
    • Identification of yeast Rho1p GTPase as a regulatory subunit of 1,3-beta-glucan synthase
    • Qadota, H. et al. Identification of yeast Rho1p GTPase as a regulatory subunit of 1,3-beta-glucan synthase. Science 272, 279-281 (1996).
    • (1996) Science , vol.272 , pp. 279-281
    • Qadota, H.1
  • 32
    • 0036372571 scopus 로고    scopus 로고
    • Morphological changes of Candida albicans induced by micafungin (FK463), a water-soluble echinocandin-like lipopeptide
    • Nishiyama, Y., Uchida, K. & Yamaguchi, H. Morphological changes of Candida albicans induced by micafungin (FK463), a water-soluble echinocandin-like lipopeptide. J. Electron Microsc. 51, 247-255 (2002).
    • (2002) J. Electron Microsc , vol.51 , pp. 247-255
    • Nishiyama, Y.1    Uchida, K.2    Yamaguchi, H.3
  • 33
    • 0035996103 scopus 로고    scopus 로고
    • In vitro activity of three new triazoles and one echinocandin against Candida bloodstream isolates from cancer patients
    • Laverdiere, M., Hoban, D., Restieri, C. & Habel, F. In vitro activity of three new triazoles and one echinocandin against Candida bloodstream isolates from cancer patients. J. Antimicrob. Chemother. 50, 119-123 (2002).
    • (2002) J. Antimicrob. Chemother , vol.50 , pp. 119-123
    • Laverdiere, M.1    Hoban, D.2    Restieri, C.3    Habel, F.4
  • 34
    • 10744224705 scopus 로고    scopus 로고
    • Antifungal susceptibility survey of 2,000 bloodstream Candida isolates in the United States
    • Ostrosky-Zeichner, L. et al. Antifungal susceptibility survey of 2,000 bloodstream Candida isolates in the United States. Antimicrob. Agents Chemother. 47, 3149-3154 (2003).
    • (2003) Antimicrob. Agents Chemother , vol.47 , pp. 3149-3154
    • Ostrosky-Zeichner, L.1
  • 35
    • 0033989710 scopus 로고    scopus 로고
    • In vitro activities of a new lipopeptide antifungal agent FK463, against a variety of clinically important fungi
    • Tawara, S. et al. In vitro activities of a new lipopeptide antifungal agent FK463, against a variety of clinically important fungi. Antimicrob. Agents Chemother. 44, 57-62 (2000).
    • (2000) Antimicrob. Agents Chemother , vol.44 , pp. 57-62
    • Tawara, S.1
  • 36
    • 0033763346 scopus 로고    scopus 로고
    • In vitro antifungal activity of a novel lipopeptide antifungal agent FK463, against various fungal pathogens
    • Uchida, K., Nishiyama, Y., Yokota, N. & Yamaguchi, H. In vitro antifungal activity of a novel lipopeptide antifungal agent FK463, against various fungal pathogens. J. Antibiot. 53, 1175-1181 (2000).
    • (2000) J. Antibiot , vol.53 , pp. 1175-1181
    • Uchida, K.1    Nishiyama, Y.2    Yokota, N.3    Yamaguchi, H.4
  • 37
    • 0036249138 scopus 로고    scopus 로고
    • In vitro activity of FK463, a novel lipopeptide antifungal agent, against a variety of clinically important molds
    • Nakai, T. et al. In vitro activity of FK463, a novel lipopeptide antifungal agent, against a variety of clinically important molds. Chemotherapy 48, 78-81 (2002).
    • (2002) Chemotherapy , vol.48 , pp. 78-81
    • Nakai, T.1
  • 38
    • 12944289674 scopus 로고    scopus 로고
    • Multiechinocandin- and multiazole-resistant Candida parapsilosis isolates serially obtained during therapy for prosthetic valve endocarditis
    • Moudgal, V., Little, T., Boikov, D. & Vazquez, J. A. Multiechinocandin- and multiazole-resistant Candida parapsilosis isolates serially obtained during therapy for prosthetic valve endocarditis. Antimicrob. Agents Chemother. 49, 767-769 (2005).
    • (2005) Antimicrob. Agents Chemother , vol.49 , pp. 767-769
    • Moudgal, V.1    Little, T.2    Boikov, D.3    Vazquez, J.A.4
  • 39
    • 0035185523 scopus 로고    scopus 로고
    • Synergy, pharmacodynamics, and time-sequenced ultrastructural changes of the interaction between nikkomycin Z and the echinocandin FK463 against Aspergillus fumigatus
    • Chiou, C. C., Mavrogiorgos, N., Tillem, E., Hector, R. & Walsh, T. J. Synergy, pharmacodynamics, and time-sequenced ultrastructural changes of the interaction between nikkomycin Z and the echinocandin FK463 against Aspergillus fumigatus. Antimicrob. Agents Chemother. 45, 3310-3321 (2001).
    • (2001) Antimicrob. Agents Chemother , vol.45 , pp. 3310-3321
    • Chiou, C.C.1    Mavrogiorgos, N.2    Tillem, E.3    Hector, R.4    Walsh, T.J.5
  • 40
    • 4344660743 scopus 로고    scopus 로고
    • Successful treatment of oesophageal candidiasis by micafungin: A novel systemic antifungal agent
    • Pettengell, K., Mynhardt, J., Kluyts, T., Lau, W., Facklam, D. & Buell, D. Successful treatment of oesophageal candidiasis by micafungin: a novel systemic antifungal agent. Aliment. Pharmacol. Ther. 20, 475-481 (2004).
    • (2004) Aliment. Pharmacol. Ther , vol.20 , pp. 475-481
    • Pettengell, K.1    Mynhardt, J.2    Kluyts, T.3    Lau, W.4    Facklam, D.5    Buell, D.6
  • 41
    • 4544236835 scopus 로고    scopus 로고
    • A randomized, doubleblind, parallel-group, dose-response study of micafungin compared with fluconazole for the treatment of esophageal candidiasis in HIVpositive patients
    • de Wet, N. et al. A randomized, doubleblind, parallel-group, dose-response study of micafungin compared with fluconazole for the treatment of esophageal candidiasis in HIVpositive patients. Clin. Infect. Dis. 39, 842-849 (2004).
    • (2004) Clin. Infect. Dis , vol.39 , pp. 842-849
    • de Wet, N.1
  • 42
    • 20144387002 scopus 로고    scopus 로고
    • A randomized, double blind, comparative trial of micafungin (FK463) vs. fluconazole for the treatment of oesophageal candidiasis
    • de Wet, N. T. et al. A randomized, double blind, comparative trial of micafungin (FK463) vs. fluconazole for the treatment of oesophageal candidiasis. Aliment. Pharmacol. Ther. 21, 899-907 (2005).
    • (2005) Aliment. Pharmacol. Ther , vol.21 , pp. 899-907
    • de Wet, N.T.1
  • 43
    • 33646340174 scopus 로고    scopus 로고
    • Kanasaki, R. et al. FR209602 and related compounds, novel antifungal lipopeptides from Coleophoma crateriformis no.738. I. Taxonomy, fermentation, isolation and physico-chemical properties. J. Antibiot. 59, 137-144 (2006).
    • Kanasaki, R. et al. FR209602 and related compounds, novel antifungal lipopeptides from Coleophoma crateriformis no.738. I. Taxonomy, fermentation, isolation and physico-chemical properties. J. Antibiot. 59, 137-144 (2006).
  • 44
    • 33646337163 scopus 로고    scopus 로고
    • FR220897 and FR220899, novel antifungal lipopeptides from Coleophoma empetri no. 14573
    • Kanasaki, R. et al. FR220897 and FR220899, novel antifungal lipopeptides from Coleophoma empetri no. 14573. J. Antibiot. 59, 149-157 (2006).
    • (2006) J. Antibiot , vol.59 , pp. 149-157
    • Kanasaki, R.1
  • 45
    • 33646340708 scopus 로고    scopus 로고
    • FR227673 and FR190293, novel antifungal lipopeptides from Chalara sp. No. 22210 and Tolypocladium parasiticum No. 16616
    • Kanasaki, R. et al. FR227673 and FR190293, novel antifungal lipopeptides from Chalara sp. No. 22210 and Tolypocladium parasiticum No. 16616. J. Antibiot. 59, 158-167 (2006).
    • (2006) J. Antibiot , vol.59 , pp. 158-167
    • Kanasaki, R.1
  • 46
    • 0035735341 scopus 로고    scopus 로고
    • Chemical diversity in lipopeptide antifungal antibiotics
    • Hino, M. et al. Chemical diversity in lipopeptide antifungal antibiotics. J. Ind. Microbiol. Biotechnol. 27, 157-162 (2001).
    • (2001) J. Ind. Microbiol. Biotechnol , vol.27 , pp. 157-162
    • Hino, M.1


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