This article needs more reliable medical references for verification or relies too heavily on primary sources. (June 2016) |
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Pronunciation | /ˌkæspoʊˈfʌndʒɪn/ KAS-poh-FUN-jin |
Trade names | Cancidas |
Other names | (4R,5S)-5-[(2-Aminoethyl)amino]-N2-(10,12-dimethyltetradecanoyl)- 4-hydroxy-L-ornithyl-L-threonyl-trans-4-hydroxy-L-prolyl-(S)-4-hydroxy-4-(p-hydroxyphenyl)-L-threonyl-threo-3-hydroxy-L-ornithyl-trans-3-hydroxy-L-proline cyclic (6→1)-peptide [1]: 185 1-[(4R,5S)-5-[(2-Aminoethyl)amino]-N2-(10,12-dimethyl-1-oxotetradecyl)-4-hydroxy-L-ornithine]-5-[(3R)-3-hydroxy-L-ornithine] pneumocandin B0[2] |
AHFS/Drugs.com | Monograph |
MedlinePlus | a615001 |
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Routes of administration | Intravenous |
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Bioavailability | 100% (intravenous use only) |
Protein binding | ~97% |
Metabolism | Liver |
Elimination half-life | 9–11 hours |
Excretion | Kidney (41%), feces (35%) |
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Formula | C52H88N10O15 |
Molar mass | 1093.331 g·mol−1 |
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(what is this?) |
Caspofungin (INN;[1][4] brand name Cancidas) is a lipopeptide antifungal drug from Merck & Co., Inc..[5] It is a member of a class of antifungals termed the echinocandins.[medical citation needed] It works by inhibiting the enzyme (1→3)-β-D-glucan synthase and thereby disturbing the integrity of the fungal cell wall.[medical citation needed]
Caspofungin was the first inhibitor of fungal (1→3)-β-D-glucan synthesis to be approved by the United States Food and Drug Administration.[6] Caspofungin is administered intravenously.[2] It is on the World Health Organization's List of Essential Medicines.[7]