12-Hydroxytetradeca-4,6-dien-8,10-diynyl acetate

Details

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Internal ID 3813c3c7-3a41-45fa-b3e2-a7c119148a1e
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 12-hydroxytetradeca-4,6-dien-8,10-diynyl acetate
SMILES (Canonical) CCC(C#CC#CC=CC=CCCCOC(=O)C)O
SMILES (Isomeric) CCC(C#CC#CC=CC=CCCCOC(=O)C)O
InChI InChI=1S/C16H20O3/c1-3-16(18)13-11-9-7-5-4-6-8-10-12-14-19-15(2)17/h4-6,8,16,18H,3,10,12,14H2,1-2H3
InChI Key ZITZYVCVZFAADU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O3
Molecular Weight 260.33 g/mol
Exact Mass 260.14124450 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.22
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 12-Hydroxytetradeca-4,6-dien-8,10-diynyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 + 0.7307 73.07%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7749 77.49%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.8705 87.05%
OATP1B3 inhibitior + 0.9411 94.11%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5707 57.07%
P-glycoprotein inhibitior - 0.9137 91.37%
P-glycoprotein substrate - 0.8152 81.52%
CYP3A4 substrate + 0.5735 57.35%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8654 86.54%
CYP3A4 inhibition - 0.8102 81.02%
CYP2C9 inhibition - 0.9461 94.61%
CYP2C19 inhibition - 0.9239 92.39%
CYP2D6 inhibition - 0.9269 92.69%
CYP1A2 inhibition - 0.6982 69.82%
CYP2C8 inhibition - 0.8232 82.32%
CYP inhibitory promiscuity - 0.8240 82.40%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.7608 76.08%
Eye corrosion + 0.5440 54.40%
Eye irritation - 0.8943 89.43%
Skin irritation + 0.6409 64.09%
Skin corrosion - 0.5963 59.63%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7535 75.35%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation + 0.6371 63.71%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.7798 77.98%
Acute Oral Toxicity (c) III 0.4872 48.72%
Estrogen receptor binding + 0.5368 53.68%
Androgen receptor binding + 0.5978 59.78%
Thyroid receptor binding - 0.5614 56.14%
Glucocorticoid receptor binding + 0.6448 64.48%
Aromatase binding + 0.5840 58.40%
PPAR gamma - 0.5104 51.04%
Honey bee toxicity - 0.8329 83.29%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.4115 41.15%

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 96.19% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.90% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 92.25% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 91.84% 97.21%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.71% 94.45%
CHEMBL2581 P07339 Cathepsin D 88.91% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.94% 96.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.74% 97.29%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 82.22% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 80.08% 94.73%

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.
Cotula coronopifolia

Cross-Links

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PubChem 163069444
LOTUS LTS0114155
wikiData Q105377488