Adrenic Acid

Modify Date: 2024-01-03 20:16:42

Adrenic Acid Structure
Adrenic Acid structure
Common Name Adrenic Acid
CAS Number 28874-58-0 Molecular Weight 332.520
Density 0.9±0.1 g/cm3 Boiling Point 439.5±24.0 °C at 760 mmHg
Molecular Formula C22H36O2 Melting Point N/A
MSDS USA Flash Point 336.2±18.0 °C

 Use of Adrenic Acid


Adrenic Acid is an inflammation enhancer in non-alcoholic fatty liver disease.

 Names

Name all-cis-docosa-7,10,13,16-tetraenoic acid
Synonym More Synonyms

 Adrenic Acid Biological Activity

Description Adrenic Acid is an inflammation enhancer in non-alcoholic fatty liver disease.
Related Catalog
Target

Human Endogenous Metabolite

In Vitro Adrenic acid is produced via the elongation of arachidonic acid by ELOVL2 and 5. Interestingly, the hepatic level of free Adrenic Acid (22:4n6) is markedly higher in the CDAHFD-fed db/db mice than in the SD-fed db/db mice. In plasma, the difference in the adrenic acid level reaches statistical significance (p<0.001). It is also found that the concentrations of phospholipid species containing Adrenic Acid, such as PC or PE (40:4) (containing side chain 18:0/22:4), and LPC 22:4 (sn-1/sn-2), are also significantly increased. (sn-1/sn-2). The hepatic and plasma levels of Adrenic Acid, which is an omega 6 polyunsaturated fatty acid (PUFA), exhibit greater differences between the CDAHFD-fed db/db mice and the SD-fed db/db mice (8.6-fold higher vs. 1.6-fold higher in liver tissue, 5.3-fold higher vs. 2.2-fold higher in plasma) than those of well-known proinflammatory PUFA, such as Arachidonic Acid[1].
References

[1]. SautHoras H Nababan, et al. Adrenic acid as an inflammation enhancer in non-alcoholic fatty liver disease. Arch Biochem Biophys. 2017 Jun 1;623-624:64-75.

 Chemical & Physical Properties

Density 0.9±0.1 g/cm3
Boiling Point 439.5±24.0 °C at 760 mmHg
Molecular Formula C22H36O2
Molecular Weight 332.520
Flash Point 336.2±18.0 °C
Exact Mass 332.271515
PSA 37.30000
LogP 7.95
Vapour Pressure 0.0±2.3 mmHg at 25°C
Index of Refraction 1.498
Storage condition −20°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves
RIDADR NONH for all modes of transport
WGK Germany 3

 Articles25

More Articles
Niacin sensitivity and the arachidonic acid pathway in schizophrenia.

Schizophr. Res. 122(1-3) , 248-56, (2010)

Schizophrenia is associated with a blunted flush response to niacin. Since niacin-induced skin flushing is mediated by vasodilators derived from arachidonic acid (AA), we tested whether the blunted fl...

Adrenic acid metabolites as endogenous endothelium-derived and zona glomerulosa-derived hyperpolarizing factors.

Hypertension 55(2) , 547-54, (2010)

Adrenic acid (docosatetraenoic acid), an abundant fatty acid in the adrenal gland, is identical to arachidonic acid except for 2 additional carbons on the carboxyl end. Adrenic acid is metabolized by ...

Reevaluation of the pathway for the metabolism of 7,10,13, 16-docosatetraenoic acid to 4,7,10,13,16-docosapentaenoic acid in rat liver.

Arch. Biochem. Biophys. 317(1) , 179-84, (1995)

When rat liver microsomes were incubated with [1-14C]22:4(n-6) under standard conditions for measuring acyl-CoA desaturases, it was not possible to detect the synthesis of any 22:5(n-6). When malonyl-...

 Synonyms

adrenic acid
all-cis-7,10,13,16-Docosatetraenoic acid
7Z,10Z,13Z,16Z-docosatetraenoic acid
Docosatetraenoic acid
CIS-7,10,13,16,19-DOCOSA-TETRAENOIC ACID
all-cis-docosa-7,10,13,16-tetraenoic acid
(7Z,10Z,13Z,16Z)-7,10,13,16-Docosatetraenoic acid
cis-7,10,13,16-DocosatetraenoicAcid
DOCOSA-7Z,10Z,13Z,16Z-PENTAENOIC ACID
7,10,13,16-Docosatetraenoic acid, (7Z,10Z,13Z,16Z)-
(All-Z)-7,10,13,16-docosatetraenoic acid
CIS-7,10,13,16-DOCOSA-TETRAENOIC ACID
DOCOSA-7Z,10Z,13Z,16Z-TETRAENOIC ACID