Pentadeca-2,8,10-trien-4,6-diynal

Details

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Internal ID c137df6b-5c87-4428-a475-3ac92c870f2d
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name pentadeca-2,8,10-trien-4,6-diynal
SMILES (Canonical) CCCCC=CC=CC#CC#CC=CC=O
SMILES (Isomeric) CCCCC=CC=CC#CC#CC=CC=O
InChI InChI=1S/C15H16O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h5-8,13-15H,2-4H2,1H3
InChI Key YPZFJPARESIZMU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O
Molecular Weight 212.29 g/mol
Exact Mass 212.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.05
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pentadeca-2,8,10-trien-4,6-diynal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.6603 66.03%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Plasma membrane 0.4497 44.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8339 83.39%
OATP1B3 inhibitior + 0.9284 92.84%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7966 79.66%
P-glycoprotein inhibitior - 0.9394 93.94%
P-glycoprotein substrate - 0.8338 83.38%
CYP3A4 substrate - 0.5501 55.01%
CYP2C9 substrate - 0.7984 79.84%
CYP2D6 substrate - 0.8408 84.08%
CYP3A4 inhibition - 0.9785 97.85%
CYP2C9 inhibition - 0.8882 88.82%
CYP2C19 inhibition - 0.8940 89.40%
CYP2D6 inhibition - 0.9628 96.28%
CYP1A2 inhibition + 0.6765 67.65%
CYP2C8 inhibition - 0.8991 89.91%
CYP inhibitory promiscuity - 0.6955 69.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.5825 58.25%
Eye corrosion + 0.9832 98.32%
Eye irritation + 0.6246 62.46%
Skin irritation + 0.8939 89.39%
Skin corrosion - 0.5000 50.00%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5914 59.14%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5213 52.13%
skin sensitisation + 0.9353 93.53%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.8180 81.80%
Acute Oral Toxicity (c) III 0.7307 73.07%
Estrogen receptor binding - 0.5217 52.17%
Androgen receptor binding - 0.5459 54.59%
Thyroid receptor binding + 0.5507 55.07%
Glucocorticoid receptor binding - 0.6043 60.43%
Aromatase binding + 0.5539 55.39%
PPAR gamma - 0.6930 69.30%
Honey bee toxicity - 0.9419 94.19%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8895 88.95%

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 91.82% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.33% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 86.56% 92.86%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.12% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.99% 92.08%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.80% 96.00%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 81.40% 85.94%

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.
Bupleurum americanum

Cross-Links

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PubChem 162989626
LOTUS LTS0045815
wikiData Q105352082