Drug

D1427 | caspofungin

Molecular Formula C52H88N10O15
Molecular Weight 1093.3
Structure
State solid
Clearance * 12 mL/min [After single IV administration]
Route of elimination After single intravenous administration of [3H] caspofungin acetate, excretion of caspofungin and its metabolites in humans was 35% of dose in feces and 41% of dose in urine.
Protein binding 0.97
Half life 9-11 hours
Absorption 92% tissue distribution within 36-48 hours after intravenous infusion
Description antifungal

J

J02AX04 Caspofungin


[J02AX] Other antimycotics for systemic use


[J02A] ANTIMYCOTICS FOR SYSTEMIC USE


[J02] ANTIMYCOTICS FOR SYSTEMIC USE


[J] Antiinfectives for systemic use


Toxicity Dose Time Species Model Method Action Positive criterion Reference
LIPID PEROXIDATION Aspergillus fumigatus lipid peroxidation using the thiobarbituric acid assay: the formation of malondialdehydes (MDAs) by antifungal drug-derived ROS in A. fumigatus was determined using the thiobarbituric acid (TBA) assay. Negative 304
LIPID PEROXIDATION Aspergillus fumigatus mitochondrion-specific lipid peroxidation probe MitoPerOx Negative 304
ROS PRODUCTION 0.5mg/ml Aspergillus fumigatus oxidant-sensing fluorescent probe 2′,7′-dichlorofluorescin diacetate t Negative 304


  • DrugBank DB00520
    PubChem Compound 2826718