8-Acetyloxy-5-hydroxydodeca-2,6-dienoic acid

Details

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Internal ID 44300b00-f975-444d-8528-2ee0cd438cd9
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name 8-acetyloxy-5-hydroxydodeca-2,6-dienoic acid
SMILES (Canonical) CCCCC(C=CC(CC=CC(=O)O)O)OC(=O)C
SMILES (Isomeric) CCCCC(C=CC(CC=CC(=O)O)O)OC(=O)C
InChI InChI=1S/C14H22O5/c1-3-4-7-13(19-11(2)15)10-9-12(16)6-5-8-14(17)18/h5,8-10,12-13,16H,3-4,6-7H2,1-2H3,(H,17,18)
InChI Key OLAUQXWOXCGMJB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22O5
Molecular Weight 270.32 g/mol
Exact Mass 270.14672380 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-Acetyloxy-5-hydroxydodeca-2,6-dienoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9274 92.74%
Caco-2 - 0.5734 57.34%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.7688 76.88%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.9052 90.52%
OATP1B3 inhibitior + 0.9403 94.03%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7426 74.26%
P-glycoprotein inhibitior - 0.9523 95.23%
P-glycoprotein substrate - 0.8158 81.58%
CYP3A4 substrate + 0.5150 51.50%
CYP2C9 substrate - 0.8047 80.47%
CYP2D6 substrate - 0.9012 90.12%
CYP3A4 inhibition - 0.8382 83.82%
CYP2C9 inhibition - 0.9135 91.35%
CYP2C19 inhibition - 0.9141 91.41%
CYP2D6 inhibition - 0.9277 92.77%
CYP1A2 inhibition - 0.7313 73.13%
CYP2C8 inhibition - 0.7538 75.38%
CYP inhibitory promiscuity - 0.8910 89.10%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7215 72.15%
Carcinogenicity (trinary) Non-required 0.7686 76.86%
Eye corrosion - 0.7198 71.98%
Eye irritation - 0.8640 86.40%
Skin irritation - 0.6976 69.76%
Skin corrosion - 0.6994 69.94%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6690 66.90%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5763 57.63%
skin sensitisation - 0.6484 64.84%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.8970 89.70%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.5956 59.56%
Acute Oral Toxicity (c) III 0.8705 87.05%
Estrogen receptor binding - 0.5604 56.04%
Androgen receptor binding - 0.7390 73.90%
Thyroid receptor binding - 0.5398 53.98%
Glucocorticoid receptor binding + 0.7227 72.27%
Aromatase binding - 0.6981 69.81%
PPAR gamma - 0.6671 66.71%
Honey bee toxicity - 0.9185 91.85%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.8837 88.37%

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 95.98% 99.17%
CHEMBL2581 P07339 Cathepsin D 93.70% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 92.64% 93.56%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.71% 97.29%
CHEMBL221 P23219 Cyclooxygenase-1 90.35% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.42% 96.09%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 88.98% 97.34%
CHEMBL1907 P15144 Aminopeptidase N 88.34% 93.31%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.80% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.61% 86.33%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.68% 97.21%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.90% 100.00%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 84.30% 96.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.68% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.90% 96.00%
CHEMBL236 P41143 Delta opioid receptor 80.76% 99.35%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.73% 92.29%
CHEMBL340 P08684 Cytochrome P450 3A4 80.70% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 80.52% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.06% 91.11%

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.
Aeollanthus buchnerianus

Cross-Links

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PubChem 73996517
LOTUS LTS0007345
wikiData Q105193876