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LY 303366
Known as:
LY-303366
, LY303366
National Institutes of Health
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Related topics
Related topics
1 relation
Broader (1)
anidulafungin
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2002
Review
2002
Echinocandins: a new class of antifungal.
D. Denning
The Journal of antimicrobial chemotherapy
2002
Corpus ID: 7562690
1103, p. 371. American Society for Microbiology, Washington, DC. 5. Villanueva, A., Arathoon, E. G., Gotuzzo, E., Berman, R. S…
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Highly Cited
2000
Highly Cited
2000
Postantifungal Effects of Echinocandin, Azole, and Polyene Antifungal Agents against Candida albicans andCryptococcus neoformans
E. Ernst
,
M. Klepser
,
M. Pfaller
Antimicrobial Agents and Chemotherapy
2000
Corpus ID: 9122368
ABSTRACT The postantifungal effect (PAFE) of fluconazole, MK-0991, LY303366, and amphotericin B was determined against isolates…
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Highly Cited
1998
Highly Cited
1998
Comparison of In Vitro Activities of the New Triazole SCH56592 and the Echinocandins MK-0991 (L-743,872) and LY303366 against Opportunistic Filamentous and Dimorphic Fungi and Yeasts
A. Espinel-Ingroff
Journal of Clinical Microbiology
1998
Corpus ID: 9467636
ABSTRACT The in vitro antifungal activities of SCH56592, MK-0991, and LY303366 against 83 isolates of Acremonium strictum…
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Highly Cited
1998
Highly Cited
1998
In vitro activity of two echinocandin derivatives, LY303366 and MK-0991 (L-743,792), against clinical isolates of Aspergillus, Fusarium, Rhizopus, and other filamentous fungi.
M. Pfaller
,
F. Marco
,
S. Messer
,
R. Jones
Diagnostic microbiology and infectious disease
1998
Corpus ID: 45947430
LY303366 and MK-0991 (previously L-743,792) are new echinocandin derivatives with excellent broad-spectrum antifungal activity…
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Highly Cited
1998
Highly Cited
1998
Influence of Test Conditions on Antifungal Time-Kill Curve Results: Proposal for Standardized Methods
M. Klepser
,
E. Ernst
,
R. Lewis
,
M. Ernst
,
M. Pfaller
Antimicrobial Agents and Chemotherapy
1998
Corpus ID: 42510517
ABSTRACT This study was designed to examine the effects of antifungal carryover, agitation, and starting inoculum on the results…
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Highly Cited
1998
Highly Cited
1998
Activity of MK-0991 (L-743,872), a new echinocandin, compared with those of LY303366 and four other antifungal agents tested against blood stream isolates of Candida spp.
F. Marco
,
M. Pfaller
,
S. Messer
,
R. Jones
Diagnostic microbiology and infectious disease
1998
Corpus ID: 46392442
MK-0991 (formerly L-743,872) is a water soluble semisynthetic echinocandin that possess potent, broad-spectrum antifungal…
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Highly Cited
1998
Highly Cited
1998
Efficacy of LY303366 against Amphotericin B-Susceptible and -Resistant Aspergillus fumigatus in a Murine Model of Invasive Aspergillosis
P. Verweij
,
K. Oakley
,
J. Morrissey
,
G. Morrissey
,
D. Denning
Antimicrobial Agents and Chemotherapy
1998
Corpus ID: 28157603
ABSTRACT LY303366 is a novel antifungal echinocandin with excellent in vitro activity against Aspergillus spp. We compared four…
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Highly Cited
1997
Highly Cited
1997
In vitro susceptibilities of clinical yeast isolates to a new echinocandin derivative, LY303366, and other antifungal agents.
M. Pfaller
,
S. Messer
,
S. Coffman
Antimicrobial agents and chemotherapy
1997
Corpus ID: 9012168
LY303366 is a new semisynthetic echinocandin derivative with potent, broad-spectrum fungicidal activity. We investigated the in…
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Review
1994
Review
1994
Antibiotics that inhibit fungal cell wall development.
M. Debono
,
R. Gordee
Annual review of microbiology
1994
Corpus ID: 35981913
The discovery of antifungal agents that possess selective toxicity against the eukaryotic fungal cell remains an important…
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Highly Cited
1994
Highly Cited
1994
Morphological effects of lipopeptides against Aspergillus fumigatus correlate with activities against (1,3)-beta-D-glucan synthase.
M. Kurtz
,
I. Heath
,
J. Marrinan
,
S. Dreikorn
,
J. Onishi
,
C. Douglas
Antimicrobial Agents and Chemotherapy
1994
Corpus ID: 40845372
The lipopeptide antifungal agents, echinocandins, papulacandins, and pneumocandins, kill Candida albicans by inhibiting glucan…
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