Update on antifungals targeted to the cell wall: focus on beta-1,3-glucan synthase inhibitors.

Abstract:

:Currently available antifungal drugs for serious infections are either fungistatic and vulnerable to resistance (azoles) or fungicidal but toxic to the host (polyenes). Cell wall-acting antifungals are inherently selective and fungicidal, features that make them particularly attractive for clinical development. Three classes of such compounds, targeted respectively to chitin synthase (nikkomycins), beta-1,3-glucan synthase (echinocandins) and mannoproteins (pradimicins/benanomicins), have entered clinical development. While nikkomycins and pradimicins/benanomicins are no longer in development, echinocandins have emerged as potentially clinically useful and three compounds, caspofungin (MK-991, L-743,872), micafungin (FK-463) and anidulafungin (LY-303366) are in late clinical development (Phase II and III).

authors

Georgopapadakou NH

doi

10.1517/13543784.10.2.269

subject

Has Abstract

pub_date

2001-02-01 00:00:00

pages

269-80

issue

2

eissn

1354-3784

issn

1744-7658

journal_volume

10

pub_type

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