Palmitoil-KoA
| Palmitoil-KoA | |
|---|---|
| |
| Identifikacija | |
| CAS registarski broj | 1763-10-6 
|
| PubChem[1][2] | 986 |
| MeSH | |
| Svojstva | |
| Molekulska formula | C37H66N7O17P3S |
| Molarna masa | 1004,94 g/mol |
|
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala | |
| Infobox references | |
Palmitoil KoA je acil-KoA tioestar koji se koristi u biosintezi sfingozina[3][4]:
Palmitoil KoA je deo sistema karnitskog premeštanja, kojim se transportuju masni acil-KoA molekuli u mitohondrije radi β-oksidacije.
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Sinteza -
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- ↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519.
- ↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
- ↑ Brady, R.N., DiMari, S.J. and Snell, E.E. (1969). „Biosynthesis of sphingolipid bases. 3. Isolation and characterization of ketonic intermediates in the synthesis of sphingosine and dihydrosphingosine by cell-free extracts of Hansenula ciferri”. J. Biol. Chem. 244: 491-496. PMID 4388074.
- ↑ Stoffel, W., Le Kim, D. and Sticht, G. (1968). „Biosynthesis of dihydrosphingosine in vitro”. Hoppe-Seyler's Z. Physiol. Chem. 349: 664-670. PMID 4386961.
