8-Hydroxyheptadeca-1-ene-4,6-diyn-3-yl acetate

Details

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Internal ID 97b74526-7c7f-4a6e-b725-cb25082c709a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 8-hydroxyheptadec-1-en-4,6-diyn-3-yl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H28O3/c1-4-6-7-8-9-10-11-14-18(21)15-12-13-16-19(5-2)22-17(3)20/h5,18-19,21H,2,4,6-11,14H2,1,3H3
InChI Key PRWWUYQDFKJMBM-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C19H28O3
Molecular Weight 304.40 g/mol
Exact Mass 304.20384475 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 5.30
Atomic LogP (AlogP) 3.61
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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SCHEMBL5278657
8-hydroxyheptadeca-1-ene-4,6-diyn-3-yl acetate

2D Structure

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2D Structure of 8-Hydroxyheptadeca-1-ene-4,6-diyn-3-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 + 0.9885 98.85%
Caco-2 - 0.6171 61.71%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.6470 64.70%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9335 93.35%
OATP1B3 inhibitior + 0.8720 87.20%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6875 68.75%
P-glycoprotein inhibitior - 0.8075 80.75%
P-glycoprotein substrate - 0.7854 78.54%
CYP3A4 substrate + 0.5211 52.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8506 85.06%
CYP3A4 inhibition - 0.6162 61.62%
CYP2C9 inhibition - 0.8059 80.59%
CYP2C19 inhibition - 0.8318 83.18%
CYP2D6 inhibition - 0.9251 92.51%
CYP1A2 inhibition + 0.5745 57.45%
CYP2C8 inhibition - 0.8146 81.46%
CYP inhibitory promiscuity - 0.7746 77.46%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7215 72.15%
Carcinogenicity (trinary) Non-required 0.7232 72.32%
Eye corrosion + 0.4514 45.14%
Eye irritation - 0.8043 80.43%
Skin irritation - 0.6028 60.28%
Skin corrosion - 0.8961 89.61%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4356 43.56%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5535 55.35%
skin sensitisation + 0.8454 84.54%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.8745 87.45%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.6549 65.49%
Acute Oral Toxicity (c) III 0.5139 51.39%
Estrogen receptor binding - 0.5792 57.92%
Androgen receptor binding - 0.5636 56.36%
Thyroid receptor binding + 0.7545 75.45%
Glucocorticoid receptor binding - 0.4717 47.17%
Aromatase binding - 0.6588 65.88%
PPAR gamma - 0.4945 49.45%
Honey bee toxicity - 0.8589 85.89%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.6621 66.21%
Fish aquatic toxicity + 0.9890 98.90%

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
CHEMBL2581 P07339 Cathepsin D 95.92% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.15% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.59% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 94.51% 97.29%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.65% 92.86%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.49% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.94% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.12% 91.11%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 87.01% 100.00%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 86.82% 85.94%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.74% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.59% 97.21%
CHEMBL340 P08684 Cytochrome P450 3A4 86.17% 91.19%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.77% 91.81%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.95% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 82.28% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 80.97% 89.63%
CHEMBL256 P0DMS8 Adenosine A3 receptor 80.81% 95.93%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.80% 100.00%
CHEMBL1907 P15144 Aminopeptidase N 80.61% 93.31%
CHEMBL3837 P07711 Cathepsin L 80.22% 96.61%
CHEMBL2885 P07451 Carbonic anhydrase III 80.14% 87.45%

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.
Cussonia zimmermannii

Cross-Links

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PubChem 11702226
LOTUS LTS0222807
wikiData Q105213964