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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1989-5-10
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pubmed:abstractText |
L-671,329 is a novel, echinocandin-like natural product that possesses potent anti-Candida activity, including activity against Candida parapsilosis. The in vitro MICs of L-671,329 were comparable to aculeacin against 18 yeasts and three filamentous fungi in an agar dilution assay. L-671,329 lysed mouse red blood cells (RBCs) at a concentration of 400 micrograms/ml, but not at 50 or 12.5 micrograms/ml. Aculeacin lysed RBCs at 400 and 50 micrograms/ml. L-671,329 significantly prolonged survival of mice infected with Candida albicans (ED50 3.38 mg/kg) following twice-daily intraperitoneal dosing for five consecutive days. The prolongation observed was greater than that seen with aculeacin therapy (ED50 6.44 mg/kg). No acute or chronic toxicities of L-671,329 or aculeacin (as measured by mortality) were detected at a concentration of 100 mg/kg following intraperitoneal administration (TD50 greater than 100 mg/kg). Both L-671,329 and aculeacin eradicated cells of C. albicans from the kidneys of infected mice. L-671,329 eradicated the yeast at therapeutic concentrations of 12.5 to 100 mg/kg. Aculeacin eradicated yeast cells at therapy concentrations of 25 to 100 mg/kg. L-671,329 has potential as an anti-Candida compound.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Bacterial Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Antifungal Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Echinocandins,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides, Cyclic,
http://linkedlifedata.com/resource/pubmed/chemical/aculeacin A,
http://linkedlifedata.com/resource/pubmed/chemical/pneumocandin A(0)
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0021-8820
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
174-8
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:2647704-Animals,
pubmed-meshheading:2647704-Anti-Bacterial Agents,
pubmed-meshheading:2647704-Antifungal Agents,
pubmed-meshheading:2647704-Candida albicans,
pubmed-meshheading:2647704-Candidiasis,
pubmed-meshheading:2647704-Dose-Response Relationship, Drug,
pubmed-meshheading:2647704-Drug Evaluation, Preclinical,
pubmed-meshheading:2647704-Echinocandins,
pubmed-meshheading:2647704-Erythrocytes,
pubmed-meshheading:2647704-Female,
pubmed-meshheading:2647704-Hemolysis,
pubmed-meshheading:2647704-Kidney,
pubmed-meshheading:2647704-Liver,
pubmed-meshheading:2647704-Mice,
pubmed-meshheading:2647704-Microbial Sensitivity Tests,
pubmed-meshheading:2647704-Peptides,
pubmed-meshheading:2647704-Peptides, Cyclic
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pubmed:year |
1989
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pubmed:articleTitle |
L-671,329, a new antifungal agent. III. In vitro activity, toxicity and efficacy in comparison to aculeacin.
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pubmed:affiliation |
Department of Basic Microbiology, Merck Sharp & Dohme Research Laboratories, Rahway, N.J. 07065-0900.
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pubmed:publicationType |
Journal Article,
Comparative Study
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