[(2R)-2,3-dihydroxypropyl] (10E,12Z)-9-oxooctadeca-10,12-dienoate

Details

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Internal ID cc7ca342-8938-4337-a630-c25ea5d81d06
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name [(2R)-2,3-dihydroxypropyl] (10E,12Z)-9-oxooctadeca-10,12-dienoate
SMILES (Canonical) CCCCCC=CC=CC(=O)CCCCCCCC(=O)OCC(CO)O
SMILES (Isomeric) CCCCC/C=C\C=C\C(=O)CCCCCCCC(=O)OC[C@@H](CO)O
InChI InChI=1S/C21H36O5/c1-2-3-4-5-6-8-11-14-19(23)15-12-9-7-10-13-16-21(25)26-18-20(24)17-22/h6,8,11,14,20,22,24H,2-5,7,9-10,12-13,15-18H2,1H3/b8-6-,14-11+/t20-/m1/s1
InChI Key JQIUXUDRBWTUPQ-GDXXYQEHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H36O5
Molecular Weight 368.50 g/mol
Exact Mass 368.25627424 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 17

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2R)-2,3-dihydroxypropyl] (10E,12Z)-9-oxooctadeca-10,12-dienoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9002 90.02%
Caco-2 - 0.7375 73.75%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8192 81.92%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.8653 86.53%
OATP1B3 inhibitior + 0.9372 93.72%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.4659 46.59%
P-glycoprotein inhibitior - 0.6256 62.56%
P-glycoprotein substrate - 0.8200 82.00%
CYP3A4 substrate + 0.5468 54.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8925 89.25%
CYP3A4 inhibition - 0.6798 67.98%
CYP2C9 inhibition - 0.8870 88.70%
CYP2C19 inhibition - 0.8637 86.37%
CYP2D6 inhibition - 0.9056 90.56%
CYP1A2 inhibition - 0.6997 69.97%
CYP2C8 inhibition - 0.7523 75.23%
CYP inhibitory promiscuity - 0.9664 96.64%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.7146 71.46%
Eye corrosion - 0.9834 98.34%
Eye irritation - 0.7248 72.48%
Skin irritation - 0.8246 82.46%
Skin corrosion - 0.9653 96.53%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6745 67.45%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.9507 95.07%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.7897 78.97%
Acute Oral Toxicity (c) III 0.4646 46.46%
Estrogen receptor binding + 0.5296 52.96%
Androgen receptor binding - 0.8435 84.35%
Thyroid receptor binding - 0.6247 62.47%
Glucocorticoid receptor binding + 0.5404 54.04%
Aromatase binding - 0.8074 80.74%
PPAR gamma - 0.5375 53.75%
Honey bee toxicity - 0.9330 93.30%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.6265 62.65%
Fish aquatic toxicity + 0.9129 91.29%

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
CHEMBL230 P35354 Cyclooxygenase-2 99.63% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 98.69% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 97.52% 97.29%
CHEMBL2581 P07339 Cathepsin D 95.75% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.24% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.94% 92.86%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.42% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.10% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.60% 91.11%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 87.62% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.26% 96.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.34% 91.81%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 85.33% 85.94%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.10% 89.34%
CHEMBL340 P08684 Cytochrome P450 3A4 84.30% 91.19%
CHEMBL299 P17252 Protein kinase C alpha 84.09% 98.03%
CHEMBL5255 O00206 Toll-like receptor 4 82.77% 92.50%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 82.61% 92.88%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.44% 94.45%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.27% 100.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.29% 94.33%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 81.01% 96.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.68% 96.47%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 80.59% 82.50%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.14% 97.21%

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.
Glycine max

Cross-Links

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PubChem 162989790
LOTUS LTS0042227
wikiData Q105133504