Ascofuranone

From Wikipedia, the free encyclopedia

Ascofuranone
Chemical structure of Ascofuranone
IUPAC name 3-Chloro-5-[(2E,6E)-7-(5,5-dimethyl-4-

oxotetrahydro-2-furanyl)-3-methyl-2,6- octadien-1-yl]-4,6-dihydroxy-2-methylbenzaldehyde

Other names Ascofuranon
Identifiers
CAS number
SMILES Oc2c(C=O)c(C)c(Cl)c(O)c2C\C=C(/C)

CC\C=C(/C)[C@@H]1CC(=O)C(C)(C)O1

Properties
Molar mass 420.926 g mol-1
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox disclaimer and references

Ascofuranone is an antibiotic produced by the fungus Ascochyta visiae[1] that inhibits the Trypanosoma brucei alternative oxidase and is a lead compound in efforts to produce other drugs targeting this enzyme for the treatment of sleeping sickness.[2] The compound is effective both in vitro cell culture and in infections in mice.[1]

Ascofuranone has also been reported to have anti-tumor activity,[3] and modulate the immune system.[4]

[edit] References

  1. ^ a b Yabu Y, Yoshida A, Suzuki T, Nihei C, Kawai K, Minagawa N, Hosokawa T, Nagai K, Kita K, Ohta N (2003). "The efficacy of ascofuranone in a consecutive treatment on Trypanosoma brucei brucei in mice". Parasitol. Int. 52 (2): 155–64. doi:10.1016/S1383-5769(03)00012-6. PMID 12798927. 
  2. ^ Minagawa N, Yabu Y, Kita K, Nagai K, Ohta N, Meguro K, Sakajo S, Yoshimoto A (1997). "An antibiotic, ascofuranone, specifically inhibits respiration and in vitro growth of long slender bloodstream forms of Trypanosoma brucei brucei". Mol. Biochem. Parasitol. 84 (2): 271–80. doi:10.1016/S0166-6851(96)02797-1. PMID 9084049. 
  3. ^ Magae J, Hayasaki J, Matsuda Y, Hotta M, Hosokawa T, Suzuki S, Nagai K, Ando K, Tamura G (1988). "Antitumor and antimetastatic activity of an antibiotic, ascofuranone, and activation of phagocytes". J. Antibiot. 41 (7): 959–65. PMID 3417568. 
  4. ^ Magae J, Suzuki S, Nagai K, Yamasaki M, Ando K, Tamura G (1986). "In vitro effects of an antitumor antibiotic, ascofuranone, on the murine immune system". Cancer Res. 46 (3): 1073–8. PMID 3080231.