(8E,10E,14E,16E)-octadeca-8,10,14,16-tetraen-12-ynal

Details

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Internal ID 49c9d1b0-c02e-4a7c-9f0e-7bb4ce163f8e
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name (8E,10E,14E,16E)-octadeca-8,10,14,16-tetraen-12-ynal
SMILES (Canonical) CC=CC=CC#CC=CC=CCCCCCCC=O
SMILES (Isomeric) C/C=C/C=C/C#C/C=C/C=C/CCCCCCC=O
InChI InChI=1S/C18H24O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h2-5,8-11,18H,12-17H2,1H3/b3-2+,5-4+,9-8+,11-10+
InChI Key HKVHDZLLVOEUHB-BDPLZKCDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H24O
Molecular Weight 256.40 g/mol
Exact Mass 256.182715385 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.77
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8E,10E,14E,16E)-octadeca-8,10,14,16-tetraen-12-ynal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 + 0.7265 72.65%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Plasma membrane 0.5460 54.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8462 84.62%
OATP1B3 inhibitior + 0.9411 94.11%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6701 67.01%
P-glycoprotein inhibitior - 0.7843 78.43%
P-glycoprotein substrate - 0.8555 85.55%
CYP3A4 substrate - 0.5250 52.50%
CYP2C9 substrate - 0.7914 79.14%
CYP2D6 substrate - 0.8191 81.91%
CYP3A4 inhibition - 0.9477 94.77%
CYP2C9 inhibition - 0.8419 84.19%
CYP2C19 inhibition - 0.9206 92.06%
CYP2D6 inhibition - 0.9733 97.33%
CYP1A2 inhibition + 0.5740 57.40%
CYP2C8 inhibition - 0.9203 92.03%
CYP inhibitory promiscuity - 0.7305 73.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5000 50.00%
Carcinogenicity (trinary) Non-required 0.5921 59.21%
Eye corrosion + 0.9893 98.93%
Eye irritation + 0.5805 58.05%
Skin irritation + 0.7424 74.24%
Skin corrosion - 0.8209 82.09%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7600 76.00%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5754 57.54%
skin sensitisation + 0.8862 88.62%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.9288 92.88%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.6768 67.68%
Acute Oral Toxicity (c) III 0.8288 82.88%
Estrogen receptor binding + 0.6113 61.13%
Androgen receptor binding - 0.5802 58.02%
Thyroid receptor binding + 0.6725 67.25%
Glucocorticoid receptor binding - 0.6342 63.42%
Aromatase binding + 0.6223 62.23%
PPAR gamma + 0.6042 60.42%
Honey bee toxicity - 0.8720 87.20%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.7241 72.41%

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
CHEMBL4040 P28482 MAP kinase ERK2 93.96% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.07% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.33% 99.17%
CHEMBL2581 P07339 Cathepsin D 86.14% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 85.49% 89.63%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.33% 89.34%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.65% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 81.29% 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.
Centaurea cineraria subsp. cineraria

Cross-Links

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PubChem 15081395
LOTUS LTS0101456
wikiData Q105029989