6,9,12-Hexadecatrienoic acid

Details

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Internal ID f4f89b5f-99db-429c-9f5b-2fbedd09d37e
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (6E,9E,12E)-hexadeca-6,9,12-trienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H26O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h4-5,7-8,10-11H,2-3,6,9,12-15H2,1H3,(H,17,18)/b5-4+,8-7+,11-10+
InChI Key SBEXLJDCZSJDLW-JSIPCRQOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H26O2
Molecular Weight 250.38 g/mol
Exact Mass 250.193280068 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.88
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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C16:3n-4,7,10
LMFA01030136
(6E,9E,12E)-hexadeca-6,9,12-trienoic acid
SCHEMBL3314681
CHEBI:165478

2D Structure

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2D Structure of 6,9,12-Hexadecatrienoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.7334 73.34%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Plasma membrane 0.6593 65.93%
OATP2B1 inhibitior - 0.8530 85.30%
OATP1B1 inhibitior - 0.5572 55.72%
OATP1B3 inhibitior - 0.3398 33.98%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7005 70.05%
P-glycoprotein inhibitior - 0.8873 88.73%
P-glycoprotein substrate - 0.9580 95.80%
CYP3A4 substrate - 0.6821 68.21%
CYP2C9 substrate + 0.6276 62.76%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.9420 94.20%
CYP2C9 inhibition - 0.8602 86.02%
CYP2C19 inhibition - 0.9434 94.34%
CYP2D6 inhibition - 0.9564 95.64%
CYP1A2 inhibition + 0.7917 79.17%
CYP2C8 inhibition - 0.9298 92.98%
CYP inhibitory promiscuity - 0.9438 94.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6535 65.35%
Carcinogenicity (trinary) Non-required 0.6276 62.76%
Eye corrosion + 0.9420 94.20%
Eye irritation + 0.8507 85.07%
Skin irritation + 0.8022 80.22%
Skin corrosion + 0.5538 55.38%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6975 69.75%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.8343 83.43%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.7582 75.82%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7953 79.53%
Acute Oral Toxicity (c) IV 0.5506 55.06%
Estrogen receptor binding - 0.5514 55.14%
Androgen receptor binding - 0.9340 93.40%
Thyroid receptor binding - 0.5439 54.39%
Glucocorticoid receptor binding - 0.6161 61.61%
Aromatase binding + 0.5936 59.36%
PPAR gamma + 0.8274 82.74%
Honey bee toxicity - 0.9934 99.34%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9045 90.45%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 96.42% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.12% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.83% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 90.74% 97.00%
CHEMBL221 P23219 Cyclooxygenase-1 88.95% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.60% 96.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 5282811
LOTUS LTS0230126
wikiData Q76286186