- to
their limited oral bioavailability,
echinocandins are
administered through intravenous infusion.
Echinocandins noncompetitively inhibit beta-1,3-D-glucan...
- synthesis.
Examples include butenafine, naftifine, and terbinafine.
Echinocandins inhibit the
creation of
glucan in the
fungal cell wall by inhibiting...
-
antifungal drugs of
class echinocandins,
recommended as the
first method of
treatment against invasive candidiasis. The
three echinocandins currently licensed...
-
peripheral organs. For
invasive disease,
treatments include amphotericin B,
echinocandins, or extended-spectrum
triazole antifungals. In the
history of fungi...
-
linoleoyl side chain. It
belongs to a
class of
antifungal agents called echinocandins,
which inhibits the
synthesis of glucan, a
major component of the fungal...
- voriconazole. It is a
member of the
class of
antifungal drugs known as the
echinocandins; its
mechanism of
action is by
inhibition of (1→3)-β-D-glucan synthase...
- var.
echinulatus strain A 32204, was
discovered in
Germany in 1974;
echinocandins destabilize the
fungal cell wall by
inhibiting the
synthesis of an integral...
- can be
successfully treated with voriconazole, amphotericin B, and
echinocandins (micafungin, caspofungin, and anidulafungin).[citation needed] Cacao...
- "New
developments and
directions in the
clinical application of the
echinocandins".
Archives of Toxicology. 91 (4): 1613–1621. Bibcode:2017ArTox..91.1613C...
- fluconazole, voriconazole,
amphotericin B, and
echinocandins.
Intravenous fluconazole or an
intravenous echinocandin such as
caspofungin are
commonly used to...
