(6E,8E,14E)-hexadeca-6,8,14-trien-10,12-diynal

Details

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Internal ID d564ffa5-edd8-4f23-b04f-f77627e1513c
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name (6E,8E,14E)-hexadeca-6,8,14-trien-10,12-diynal
SMILES (Canonical) CC=CC#CC#CC=CC=CCCCCC=O
SMILES (Isomeric) C/C=C/C#CC#C/C=C/C=C/CCCCC=O
InChI InChI=1S/C16H18O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h2-3,8-11,16H,12-15H2,1H3/b3-2+,9-8+,11-10+
InChI Key NDAPUMLRLFELHL-MMOYHAHMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H18O
Molecular Weight 226.31 g/mol
Exact Mass 226.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.44
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6E,8E,14E)-hexadeca-6,8,14-trien-10,12-diynal

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 + 0.7446 74.46%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Plasma membrane 0.4744 47.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8212 82.12%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8106 81.06%
P-glycoprotein inhibitior - 0.9293 92.93%
P-glycoprotein substrate - 0.8314 83.14%
CYP3A4 substrate - 0.5275 52.75%
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 - 0.9298 92.98%
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 - 0.4886 48.86%
Skin irritation + 0.8207 82.07%
Skin corrosion - 0.6265 62.65%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5912 59.12%
skin sensitisation + 0.8578 85.78%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.7658 76.58%
Acute Oral Toxicity (c) III 0.8427 84.27%
Estrogen receptor binding + 0.5875 58.75%
Androgen receptor binding - 0.5728 57.28%
Thyroid receptor binding - 0.5167 51.67%
Glucocorticoid receptor binding - 0.5752 57.52%
Aromatase binding + 0.6009 60.09%
PPAR gamma + 0.6430 64.30%
Honey bee toxicity - 0.8667 86.67%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5500 55.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.74% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.27% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.42% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.13% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.68% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 80.90% 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 pullata
Pleiotaxis rugosa
Volutaria muricata

Cross-Links

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PubChem 14412233
LOTUS LTS0102384
wikiData Q105177465