The novel oral glucan synthase inhibitor SCY-078 shows in vitro activity against sessile and planktonic Candida spp.
Author(s) -
Laura Judith Marcos-Zambrano,
Marta GomezPerosanz,
Pilar Escribano,
Emilio Bouza,
Jesús Guinea
Publication year - 2017
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkx010
Subject(s) - micafungin , candida glabrata , candida parapsilosis , microbiology and biotechnology , fluconazole , candida albicans , candida tropicalis , biofilm , in vitro , echinocandins , biology , antifungal , biochemistry , bacteria , caspofungin , genetics
We studied the antifungal activity of SCY-078 (an orally bioavailable 1,3-β -d- glucan synthesis inhibitor), micafungin and fluconazole against the planktonic and sessile forms of 178 Candida and non- Candida isolates causing fungaemia in patients recently admitted to a large European hospital.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom