https://pubchem.ncbi.nlm.nih.gov/compound/2-Hydroxytetracosanoic_acid#section=Top
C24H48O
Tämä rasvahappo vaatii oksidaatiossaan alfa-oksidaation, mistä voi tulla jollekin yksilöille ongelmaa alfa-oksidaation heikkouden takia. se vaatii peroksisomaalisen oksidaation.
https://www.ncbi.nlm.nih.gov/pubmed/11104019
Tällä rasvahappomuodolla näyttää oelvan useampiakin merkityksiä tautipuolella.
Tällä hapolla on paljon synonyymisiä nimiä:
- 2-Hydroxytetracosanoic acid
- Cerebronic acid
- 544-57-0
- Phrenosic acid
- Phrenosinic acid
- DL-Cerebronic acid
- 2-hydroxy-tetracosanoic acid
- Cerebronsaeure
- acide cerebronique
- a-hydroxylignoceric acid
- 2-hydroxylignoceric acid
- AC1L2SRS
- 2-Hydroxy-tetracosansaeure
- 2-hydroxytetraicosanoic acid
- AC1Q5ST6
- 2-hydroxytetraeicosanoic acid
- SCHEMBL338278
- CHEBI:61302
- CTK6D9796
- LMFA01050080Haen hakusanalla phrenosic acid lisätietoja.http://www.hmdb.ca/metabolites/HMDB0039540
DL-Cerebronic acid, also known as acide cerebronique or cerebronsaeure, belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms.
DL-Cerebronic acid is considered to be a practically insoluble (in water) and relatively neutral molecule. DL-Cerebronic acid has been primarily detected in urine. Within the cell, DL-cerebronic acid is primarily located in the membrane (predicted from logP), cytoplasm and adiposome. DL-Cerebronic acid participates in a number of enzymatic reactions. In particular, DL-cerebronic acid can be biosynthesized from tetracosanoic acid. DL-Cerebronic acid is also a parent compound for other transformation products, including but not limited to, N-2-hydroxylignoceroylsphingosine, 2-hydroxytetracosanoyl-CoA, and N-(2-hydroxylignoceroyl)-D-galactosylsphingosine. Outside of the human body, DL-cerebronic acid can be found in mushrooms. This makes DL-cerebronic acid a potential biomarker for the consumption of this food product.
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