| Weight | 328.496 g/mol |
|---|---|
| Formula | C22H32O2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 14 |
Docosahexaenoic acid (6217-54-5)
Score:
#683 in Neuroscience
,
#1209 in Biochemistry
,
#3038 in Biology
,
#3796 in Chemistry
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- Sigma-Aldrich - Docosahexaenoic acid44.10 - 404.00 USD
- Fisher Scientific - Search for Docosahexaenoic acid
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- HEALTH BENEFITS OF DOCOSAHEXAENOIC ACID DHA (Pharmacological Research, 1999)
- Novel docosatrienes and 17S-resolvins generated from docosahexaenoic acid in murine brain, human blood, and glial cells. Autacoids in anti-inflammation. (Journal of Biological Chemistry, 2003)
- Mechanisms of action of docosahexaenoic acid in the nervous system (Lipids, 2001)
- Docosahexaenoic Acid, a Ligand for the Retinoid X Receptor in Mouse Brain (Science, 2000)
- A role for docosahexaenoic acidderived neuroprotectin D1 in neural cell survival and Alzheimer disease (Journal of Clinical Investigation, 2005)
- Docosahexaenoic Acid Protects from Dendritic Pathology in an Alzheimer's Disease Mouse Model (Neuron, 2004)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC=CCC=CCC=CCC=CCC=CCC=CCCC(=O)O
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InChIKeyMBMBGCFOFBJSGT-UHFFFAOYSA-N
- Pubchem - Docosahexaenoic acid
- Wikipedia - doconexent
Docosahexaenoic acid (DHA) is an omega-3 fatty acid that is a primary structural component of the human brain, cerebral cortex, skin, and retina. It can be synthesized from alpha-linolenic acid or obtained directly from maternal milk (breast milk), fish oil, or algae oil. DHA's structure is a carboxylic acid (-oic acid) with a 22-carbon chain (docosa- derives from the Ancient Greek for 22) and six (hexa-) cis double bonds (-en-); with the first double bond located at the third carbon from the omega end.
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Docosahexaenoic acid
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