| Weight | 924.091 g/mol |
|---|---|
| Formula | C47H73NO17 |
| Hydrogen Acceptors | 17 |
| Hydrogen Donors | 12 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Fungizone (1397-89-3)
Score:
#94 in Microbiology
,
#300 in Biochemistry
,
#1109 in Biology
,
#1249 in Chemistry
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- Prophylactic efficacy of aerosolized liposomal (AmBisome) and non-lipsomal (Fungizone) amphotericin B in murine pulmonary aspergillosis (Journal of Antimicrobial Chemotherapy, 1994)
- Biodegradable Nanoparticles Improve Oral Bioavailability of Amphotericin B and Show Reduced Nephrotoxicity Compared to Intravenous Fungizone (Pharmaceutical Research, 2009)
- Effects of streptomycin, cycloheximide, fungizone, captan, carbofuran, cygon, and PCNB on soil microorganisms (Microbial Ecology, 1984)
- Liposomal amphotericin B (AmBisome) reduces dissemination of infection as compared with amphotericin B deoxycholate (Fungizone) in a rate model of pulmonary aspergillosis. (Journal of Antimicrobial Chemotherapy, 1996)
- Comparison of Fungizone, Amphotec, AmBisome, and Abelcet for Treatment of Systemic Murine Cryptococcosis (Antimicrobial Agents and Chemotherapy, 1998)
- Biodistribution of liposomal amphotericin B (AmBisome) and amphotericin B-desoxycholate (Fungizone) in uninfected immunocompetent mice and leucopenic mice infected with Candida albicans (Journal of Antimicrobial Chemotherapy, 1995)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1C=CC=CC=CC=CC=CC=CC=CC(CC2C(C(CC(O2)(CC(CC(C(CCC(CC(CC(=O)OC(C(C1O)C)C)O)O)O)O)O)O)O)C(=O)O)OC3C(C(C(C(O3)C)O)N)O
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InChIKeyAPKFDSVGJQXUKY-UHFFFAOYSA-N
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