Docosa-4,7,10,13,16,19-hexaenoic acid

Details

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Internal ID e312d109-3d95-4304-83b9-cd35b1b690a1
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Very long-chain fatty acids
IUPAC Name docosa-4,7,10,13,16,19-hexaenoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h3-4,6-7,9-10,12-13,15-16,18-19H,2,5,8,11,14,17,20-21H2,1H3,(H,23,24)
InChI Key MBMBGCFOFBJSGT-UHFFFAOYSA-N
Popularity 4,116 references in papers

Physical and Chemical Properties

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Molecular Formula C22H32O2
Molecular Weight 328.50 g/mol
Exact Mass 328.240230259 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 6.20
Atomic LogP (AlogP) 6.55
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 14

Synonyms

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4,7,10,13,16,19-Docosahexaenoic acid, (4Z,7Z,10Z,13Z,16Z,19Z)-
DHA;Cervonic Acid
4,7,10,13,16,19-Docosahexaenoic acid
MFCD00065722
CBiol_001946
KBioGR_000018
KBioSS_000018
KBio2_000018
KBio2_002586
KBio2_005154
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Docosa-4,7,10,13,16,19-hexaenoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 - 0.7582 75.82%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Plasma membrane 0.6160 61.60%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior - 0.3607 36.07%
OATP1B3 inhibitior - 0.2579 25.79%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8783 87.83%
P-glycoprotein inhibitior - 0.6248 62.48%
P-glycoprotein substrate - 0.9781 97.81%
CYP3A4 substrate - 0.7269 72.69%
CYP2C9 substrate + 0.6276 62.76%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.9440 94.40%
CYP2C9 inhibition - 0.9094 90.94%
CYP2C19 inhibition - 0.9717 97.17%
CYP2D6 inhibition - 0.9640 96.40%
CYP1A2 inhibition + 0.6216 62.16%
CYP2C8 inhibition - 0.9687 96.87%
CYP inhibitory promiscuity - 0.9588 95.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6435 64.35%
Carcinogenicity (trinary) Non-required 0.6635 66.35%
Eye corrosion + 0.9532 95.32%
Eye irritation - 0.6852 68.52%
Skin irritation + 0.7514 75.14%
Skin corrosion - 0.7017 70.17%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4512 45.12%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.8625 86.25%
skin sensitisation + 0.8140 81.40%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.7219 72.19%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.8449 84.49%
Acute Oral Toxicity (c) IV 0.6395 63.95%
Estrogen receptor binding + 0.7041 70.41%
Androgen receptor binding - 0.9209 92.09%
Thyroid receptor binding - 0.5946 59.46%
Glucocorticoid receptor binding + 0.6682 66.82%
Aromatase binding + 0.6192 61.92%
PPAR gamma + 0.7960 79.60%
Honey bee toxicity - 0.9901 99.01%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.7885 78.85%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.11% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.98% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.37% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 87.98% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.80% 86.33%
CHEMBL1781 P11387 DNA topoisomerase I 80.07% 97.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 3144
LOTUS LTS0212289
wikiData Q105160840