6-Acetyloxytrideca-1,3,11-trien-7,9-diyn-5-yl acetate

Details

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Internal ID d9ba1121-9b2d-47b3-9964-c5e26237a812
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 6-acetyloxytrideca-1,3,11-trien-7,9-diyn-5-yl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H18O4/c1-5-7-9-10-11-13-17(21-15(4)19)16(12-8-6-2)20-14(3)18/h5-8,12,16-17H,2H2,1,3-4H3
InChI Key QHOZIKGCMAXNBQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O4
Molecular Weight 286.32 g/mol
Exact Mass 286.12050905 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.17
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Acetyloxytrideca-1,3,11-trien-7,9-diyn-5-yl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9501 95.01%
Caco-2 - 0.6473 64.73%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.7700 77.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8717 87.17%
OATP1B3 inhibitior + 0.9570 95.70%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.4598 45.98%
P-glycoprotein inhibitior - 0.7208 72.08%
P-glycoprotein substrate - 0.8665 86.65%
CYP3A4 substrate + 0.5599 55.99%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.8808 88.08%
CYP3A4 inhibition - 0.5276 52.76%
CYP2C9 inhibition - 0.8843 88.43%
CYP2C19 inhibition - 0.8645 86.45%
CYP2D6 inhibition - 0.9528 95.28%
CYP1A2 inhibition - 0.8854 88.54%
CYP2C8 inhibition - 0.8033 80.33%
CYP inhibitory promiscuity - 0.8610 86.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5607 56.07%
Carcinogenicity (trinary) Non-required 0.6650 66.50%
Eye corrosion + 0.8373 83.73%
Eye irritation - 0.8560 85.60%
Skin irritation - 0.6023 60.23%
Skin corrosion - 0.6971 69.71%
Ames mutagenesis + 0.5363 53.63%
Human Ether-a-go-go-Related Gene inhibition - 0.4056 40.56%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.5211 52.11%
skin sensitisation + 0.9255 92.55%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.7498 74.98%
Acute Oral Toxicity (c) III 0.5603 56.03%
Estrogen receptor binding + 0.5770 57.70%
Androgen receptor binding - 0.7082 70.82%
Thyroid receptor binding + 0.5831 58.31%
Glucocorticoid receptor binding - 0.5314 53.14%
Aromatase binding - 0.6691 66.91%
PPAR gamma - 0.4894 48.94%
Honey bee toxicity + 0.6027 60.27%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5755 57.55%
Fish aquatic toxicity + 0.9392 93.92%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.32% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.27% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 85.38% 91.49%
CHEMBL2581 P07339 Cathepsin D 85.17% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.16% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.51% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 81.10% 91.19%

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.
Atractylodes lancea

Cross-Links

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PubChem 163037292
LOTUS LTS0179514
wikiData Q105221061