Hexadeca-6,8,12,14-tetraen-10-ynal

Details

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Internal ID 57de27a2-8af8-4786-a57e-8b0ea1416bc0
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name hexadeca-6,8,12,14-tetraen-10-ynal
SMILES (Canonical) CC=CC=CC#CC=CC=CCCCCC=O
SMILES (Isomeric) CC=CC=CC#CC=CC=CCCCCC=O
InChI InChI=1S/C16H20O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h2-5,8-11,16H,12-15H2,1H3
InChI Key JSONUWKRCNXRBR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O
Molecular Weight 228.33 g/mol
Exact Mass 228.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.99
H-Bond Acceptor 1
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 Hexadeca-6,8,12,14-tetraen-10-ynal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9880 98.80%
Caco-2 + 0.7860 78.60%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Plasma membrane 0.4744 47.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8264 82.64%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6116 61.16%
P-glycoprotein inhibitior - 0.9132 91.32%
P-glycoprotein substrate - 0.8658 86.58%
CYP3A4 substrate - 0.5397 53.97%
CYP2C9 substrate - 0.7914 79.14%
CYP2D6 substrate - 0.8191 81.91%
CYP3A4 inhibition - 0.9293 92.93%
CYP2C9 inhibition - 0.8608 86.08%
CYP2C19 inhibition - 0.9101 91.01%
CYP2D6 inhibition - 0.9713 97.13%
CYP1A2 inhibition + 0.5885 58.85%
CYP2C8 inhibition - 0.9328 93.28%
CYP inhibitory promiscuity - 0.6972 69.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.5195 51.95%
Eye corrosion + 0.9916 99.16%
Eye irritation + 0.6307 63.07%
Skin irritation + 0.8207 82.07%
Skin corrosion - 0.6265 62.65%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4752 47.52%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5912 59.12%
skin sensitisation + 0.8578 85.78%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6760 67.60%
Acute Oral Toxicity (c) III 0.8427 84.27%
Estrogen receptor binding + 0.7786 77.86%
Androgen receptor binding - 0.6188 61.88%
Thyroid receptor binding + 0.6320 63.20%
Glucocorticoid receptor binding - 0.5141 51.41%
Aromatase binding + 0.6596 65.96%
PPAR gamma + 0.6296 62.96%
Honey bee toxicity - 0.8671 86.71%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity - 0.4626 46.26%

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 89.75% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.42% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.04% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.65% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.13% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.83% 89.34%
CHEMBL230 P35354 Cyclooxygenase-2 81.53% 89.63%
CHEMBL3401 O75469 Pregnane X receptor 81.14% 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 85626717
LOTUS LTS0210986
wikiData Q105134482