Cerulenin
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| Names | |
|---|---|
| IUPAC name
(2R,3S)-3-[(4E,7E)-nona-4,7-dienoyl]oxirane-2-carboxamide | |
| Identifiers | |
17397-89-6  | |
| ChEBI | CHEBI:171741  |
| ChEMBL | ChEMBL45627 |
| ChemSpider | 4445281 |
| DrugBank | DB01034 |
| Jmol interactive 3D | Image |
| KEGG | C12058 |
| PubChem | 5282054 |
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| Properties | |
| C12H17NO3 | |
| Molar mass | 223.2695 |
| Density | 1.135 g/mL |
| Boiling point | 456.14 °C (853.05 °F; 729.29 K) |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| Infobox references | |
Cerulenin is an antifungal antibiotic that inhibits fatty acid and steroid biosynthesis. In fatty acid synthesis, it has been reported to bind in equimolar ratio to b-keto-acyl-ACP synthase, one of the seven moieties of fatty acid synthase, blocking the interaction of malonyl-CoA. It also has the related activity of stimulating fatty acid oxidation through the activation of CPT1, another enzyme normally inhibited by malonyl-CoA. Inhibition involves covalent thioacylation that permanently inactivates the enzymes.[1] These two behaviors may increase the availability of energy in the form of ATP, perhaps sensed by AMPK, in the hypothalamus.[2]
In sterol synthesis, cerulenin inhibits HMG-CoA synthetase activity.[3] It was also reported that cerulenin specifically inhibited fatty acid biosynthesis in Saccharomyces cerevisiae without having an effect on sterol formation.[3] But in general conclusion, cerulenin has inhibitory effects on sterol synthesis.
Cerulenin causes a dose-dependent decrease in HER2/neu protein levels in breast cancer cells, from 14% at 1.25 to 78% at 10 milligrams per liter, and targeting of fatty acid synthase by related drugs has been suggested as a possible treatment.[4] Antiproliferative and pro-apoptotic effects have been shown in colon cells as well.[5] At an intraperitoneal dose of 30 milligrams per kilogram, it has been shown to inhibit feeding and induce dramatic weight loss in mice by a mechanism similar to, but independent or downstream of, leptin signaling.[6] It is found naturally in the industrial strain Cephalosporium caerulens (Sarocladium oryzae, the sheath rot pathogen of rice).
External links
References
- ↑ Straub SG, Yajima H, Komatsu M, Aizawa T, Sharp GW (February 2002). "The effects of cerulenin, an inhibitor of protein acylation, on the two phases of glucose-stimulated insulin secretion". Diabetes. 51 Suppl 1 (90001): S91–5. doi:10.2337/diabetes.51.2007.S91. PMID 11815464.
- ↑ Reviewed in Ronnett GV, Kleman AM, Kim EK, Landree LE, Tu Y (August 2006). "Fatty acid metabolism, the central nervous system, and feeding". Obesity (Silver Spring). 14 Suppl 5: 201S–207S. doi:10.1038/oby.2006.309. PMID 17021367.
- 1 2 Ohno T, Awaya J, Kesado T, Nomura S, Omura S (October 1974). "Mechanism of Action of CM-55, a Synthetic Analogue of the Antilipogenic Antibiotic Cerulenin". Antimicrob. Agents Chemother. 6 (4): 387–92. doi:10.1128/aac.6.4.387. PMC 444657. PMID 4157441.
- ↑ Menendez JA, Vellon L, Mehmi I; et al. (July 2004). "Inhibition of fatty acid synthase (FAS) suppresses HER2/neu (erbB-2) oncogene overexpression in cancer cells". Proc. Natl. Acad. Sci. U.S.A. 101 (29): 10715–20. doi:10.1073/pnas.0403390101. PMC 490000. PMID 15235125.
- ↑ Huang P, Zhu S, Lu S, Dai Z, Jin Y (April 2000). "[An experimental study on cerulenin induced apoptosis of human colonic cancer cells]". Zhonghua Bing Li Xue Za Zhi (in Chinese) 29 (2): 115–8. PMID 11866903.
- ↑ Ghosh MK, Amudha R, Jayachandran S, Sakthivel N (2002). "Detection and quantification of phytotoxic metabolites of Sarocladium oryzae in sheath rot-infected grains of rice". Lett. Appl. Microbiol. 34 (6): 398–401. doi:10.1046/j.1472-765X.2002.01111.x. PMID 12028418.