3-Acetyloxytetradeca-6,12-dien-8,10-diynyl acetate

Details

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Internal ID d8b6846b-35ee-4e01-b30e-362b6fb774e4
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 3-acetyloxytetradeca-6,12-dien-8,10-diynyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H22O4/c1-4-5-6-7-8-9-10-11-12-13-18(22-17(3)20)14-15-21-16(2)19/h4-5,10-11,18H,12-15H2,1-3H3
InChI Key QQRFFZAYQSFFQP-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H22O4
Molecular Weight 302.40 g/mol
Exact Mass 302.15180918 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.79
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Acetyloxytetradeca-6,12-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 + 0.9693 96.93%
Caco-2 + 0.5379 53.79%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.8530 85.30%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.8586 85.86%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5363 53.63%
P-glycoprotein inhibitior - 0.7549 75.49%
P-glycoprotein substrate - 0.8148 81.48%
CYP3A4 substrate + 0.5687 56.87%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8720 87.20%
CYP3A4 inhibition - 0.6247 62.47%
CYP2C9 inhibition - 0.7747 77.47%
CYP2C19 inhibition - 0.8519 85.19%
CYP2D6 inhibition - 0.9219 92.19%
CYP1A2 inhibition - 0.7683 76.83%
CYP2C8 inhibition - 0.8477 84.77%
CYP inhibitory promiscuity - 0.7443 74.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6123 61.23%
Carcinogenicity (trinary) Non-required 0.7174 71.74%
Eye corrosion - 0.6205 62.05%
Eye irritation - 0.9582 95.82%
Skin irritation - 0.6164 61.64%
Skin corrosion - 0.9794 97.94%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8188 81.88%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.6218 62.18%
skin sensitisation - 0.8215 82.15%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.7570 75.70%
Acute Oral Toxicity (c) III 0.6983 69.83%
Estrogen receptor binding + 0.6514 65.14%
Androgen receptor binding - 0.6264 62.64%
Thyroid receptor binding + 0.5434 54.34%
Glucocorticoid receptor binding + 0.6218 62.18%
Aromatase binding - 0.5325 53.25%
PPAR gamma + 0.5834 58.34%
Honey bee toxicity - 0.7432 74.32%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9618 96.18%

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 93.14% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.01% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.69% 96.00%
CHEMBL2581 P07339 Cathepsin D 83.25% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 82.66% 94.73%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 82.61% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.68% 94.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.50% 89.34%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.45% 95.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.31% 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.
Coreopsis capillacea

Cross-Links

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PubChem 54242007
LOTUS LTS0106766
wikiData Q105226007