Палмитоил-КоА
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| Identifikacija | |
|---|---|
| ECHA InfoCard | 100.015.616 |
| MeSH | Palmitoyl+Coenzyme+A |
| Svojstva | |
| C37H66N7O17P3S | |
| Molarna masa | 1004,94 g/mol |
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa). | |
 verifikuj (šta je   ?)
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| Reference infokutije | |
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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Reference[уреди | уреди извор]
- ^ 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. PMID 20970519. doi:10.1016/j.drudis.2010.10.003.
- ^ 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.
