- 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...
-
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...
-
peripheral organs. For
invasive disease,
treatments include amphotericin B,
echinocandins, or extended-spectrum
triazole antifungals. In the
history of fungi...
- 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...
- from
Glarea lozoyensis. Strobilurin, azoxystrobin, micafungin, and
echinocandins, are all
extracted from fungi.
Anidulafungin is a
derivative of an Aspergillus...
- can be
successfully treated with voriconazole, amphotericin B, and
echinocandins (micafungin, caspofungin, and anidulafungin).[citation needed] Cacao...
-
resistant to
amphotericin B; however, most
isolates are
susceptible to
echinocandins.
Treatment is
complicated because C. auris is
easily misidentified as...
-
Merck & Co., Inc.. It is a
member of a
class of
antifungals termed the
echinocandins.[medical
citation needed] It
works by
inhibiting the
enzyme (1→3)-β-D-glucan...
