Fumagillin
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Systematic (IUPAC) name | |
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(2E,4E,6E,8E)-10-{[(3R,4S,5S,6R)-5-methoxy- 4-[(2R)-2-methyl-3-(3-methylbut-2-enyl)oxiran-2-yl]-1- oxaspiro[2.5]octan-6-yl]oxy}-10 -oxodeca-2,4,6,8-tetraenoic acid
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Clinical data | |
AHFS/Drugs.com | International Drug Names |
Identifiers | |
CAS Number | 23110-15-8 ![]() |
ATC code | P01AX10 (WHO) QP51AX23 (WHO) |
PubChem | CID: 6917655 |
DrugBank | DB02640 ![]() |
ChemSpider | 5292885 ![]() |
UNII | 7OW73204U1 ![]() |
ChEBI | CHEBI:48635 ![]() |
ChEMBL | CHEMBL32838 ![]() |
Chemical data | |
Formula | C26H34O7 |
Molecular mass | 458.54 g/mol |
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Fumagillin is a complex biomolecule and used as an antimicrobial agent. It was isolated in 1949 from the microbial organism Aspergillus fumigatus.[1]
Uses
In animals
It was originally used against microsporidial parasites Nosema apis infections in honey bees.
Some studies found it to be effective against some myxozoan parasites, including Myxobolus cerebralis, an important parasite of fish; however, in the more rigorous tests required for U.S. Food and Drug Administration approval, it was ineffective.
There are reports that fumagillin controls Nosema ceranae,[2] which has recently been hypothesized as a possible cause of colony collapse disorder.[3][4] The latest report, however, has shown it to be ineffective against N. ceranae.[5] Fumagillin is also investigated as an inhibitor of malaria parasite growth.[6][7]
In humans
Fumagillin has been used in the treatment of microsporidiosis.[8][9] It is also an amebicide.[10]
Fumagillin can block blood vessel formation by binding to an enzyme methionine aminopeptidase 2[11] and for this reason, the compound, together with semisynthetic derivatives, are investigated as an angiogenesis inhibitor [12] in the treatment of cancer.
Preliminary clinical trials are being conducted by Zafgen into using the fumagillin analog beloranib for weight loss.[13]
According to Zbidah and coworkers from Germany fumagillin is toxic to erythrocytes in vitro.[14]
Total synthesis
Fumagillin and the related fumagillol (the hydrolysis product) have been a target in total synthesis, with several reported successful strategies, racemic, asymmetric and formal.[15][16][17][18][19][20][21][22][23]
References
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- ↑ F. R. Hanson, T. E. Elbe, J. Bacteriol. 1949, 58, 527
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- ↑ Xiaochun Chen et al. "Fumagillin and Fumarranol Interact with P. falciparum Methionine Aminopeptidase 2 and Inhibit Malaria Parasite Growth In Vitro and In Vivo". Chemistry & Biology, Vol. 16 Nr. 2 (2009) blz. 193-202. Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Christopher Arico-Muendel et al. "Antiparasitic activities of novel, orally available fumagillin analogs". Bioorganic & Medicinal Chemistry Letters Vol. 19 Nr. 17 (2009), blz. 5128-5131 Lua error in package.lua at line 80: module 'strict' not found.
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- ↑ A Concise Synthesis of Fumagillol David A. Vosburg, Sven Weiler, Erik J. Sorensen Angewandte Chemie International Edition Volume 38, Issue 7, Date: April 1, 1999, Pages: 971-974 DOI
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- Epoxides
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- Wikipedia articles needing factual verification from December 2009