6,8,10,12-Pentadecatetraenal

Details

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Internal ID 047c9ec2-6cdf-4e2f-8fc4-b3a64bde13ae
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name (6E,8E,10E,12E)-pentadeca-6,8,10,12-tetraenal
SMILES (Canonical) CCC=CC=CC=CC=CCCCCC=O
SMILES (Isomeric) CC/C=C/C=C/C=C/C=C/CCCCC=O
InChI InChI=1S/C15H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h3-10,15H,2,11-14H2,1H3/b4-3+,6-5+,8-7+,10-9+
InChI Key ZSDGTOPNWLXOHV-BYFNFPHLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.38
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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LMFA06000087
(6E,8E,10E,12E)-pentadeca-6,8,10,12-tetraenal
SCHEMBL22498747
SCHEMBL22498748
CHEBI:165521

2D Structure

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2D Structure of 6,8,10,12-Pentadecatetraenal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.9334 93.34%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Plasma membrane 0.6096 60.96%
OATP2B1 inhibitior - 0.8622 86.22%
OATP1B1 inhibitior + 0.8612 86.12%
OATP1B3 inhibitior + 0.9394 93.94%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5185 51.85%
P-glycoprotein inhibitior - 0.9329 93.29%
P-glycoprotein substrate - 0.9013 90.13%
CYP3A4 substrate - 0.6320 63.20%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8090 80.90%
CYP3A4 inhibition - 0.9710 97.10%
CYP2C9 inhibition - 0.9112 91.12%
CYP2C19 inhibition - 0.9295 92.95%
CYP2D6 inhibition - 0.9676 96.76%
CYP1A2 inhibition + 0.6149 61.49%
CYP2C8 inhibition - 0.9624 96.24%
CYP inhibitory promiscuity - 0.7305 73.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.6012 60.12%
Eye corrosion + 0.9950 99.50%
Eye irritation + 0.9158 91.58%
Skin irritation + 0.8197 81.97%
Skin corrosion - 0.9407 94.07%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3847 38.47%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation + 0.8980 89.80%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5702 57.02%
Acute Oral Toxicity (c) III 0.9159 91.59%
Estrogen receptor binding + 0.7127 71.27%
Androgen receptor binding - 0.7174 71.74%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.6463 64.63%
Aromatase binding + 0.6437 64.37%
PPAR gamma - 0.5239 52.39%
Honey bee toxicity - 0.9398 93.98%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity - 0.4440 44.40%

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 87.99% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.43% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.65% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.90% 99.17%
CHEMBL2664 P23526 Adenosylhomocysteinase 82.42% 86.67%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.61% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 80.14% 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
Centaurea solstitialis

Cross-Links

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PubChem 5283373
LOTUS LTS0043190
wikiData Q76294041