(E)-2-ethylnonacos-2-enal

Details

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Internal ID eb5b2bd5-d4b1-4b17-b40a-7cd0ff79fe83
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name (E)-2-ethylnonacos-2-enal
SMILES (Canonical) CCCCCCCCCCCCCCCCCCCCCCCCCCC=C(CC)C=O
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCCCCCCCCC/C=C(\CC)/C=O
InChI InChI=1S/C31H60O/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-31(4-2)30-32/h29-30H,3-28H2,1-2H3/b31-29+
InChI Key OGSVWBDEBNOQIG-OWWNRXNESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H60O
Molecular Weight 448.80 g/mol
Exact Mass 448.464416533 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 14.80
Atomic LogP (AlogP) 11.29
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 27

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E)-2-ethylnonacos-2-enal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 - 0.5141 51.41%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.3038 30.38%
OATP2B1 inhibitior - 0.8519 85.19%
OATP1B1 inhibitior + 0.8805 88.05%
OATP1B3 inhibitior + 0.9267 92.67%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.4925 49.25%
P-glycoprotein inhibitior - 0.6462 64.62%
P-glycoprotein substrate - 0.9357 93.57%
CYP3A4 substrate - 0.6465 64.65%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.8311 83.11%
CYP3A4 inhibition - 0.9778 97.78%
CYP2C9 inhibition - 0.9349 93.49%
CYP2C19 inhibition - 0.9464 94.64%
CYP2D6 inhibition - 0.9487 94.87%
CYP1A2 inhibition + 0.5225 52.25%
CYP2C8 inhibition - 0.8641 86.41%
CYP inhibitory promiscuity - 0.6469 64.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.5861 58.61%
Eye corrosion + 0.8917 89.17%
Eye irritation + 0.8298 82.98%
Skin irritation + 0.8111 81.11%
Skin corrosion - 0.8916 89.16%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4658 46.58%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5515 55.15%
skin sensitisation + 0.9652 96.52%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5383 53.83%
Acute Oral Toxicity (c) III 0.8186 81.86%
Estrogen receptor binding + 0.5568 55.68%
Androgen receptor binding - 0.7624 76.24%
Thyroid receptor binding + 0.6454 64.54%
Glucocorticoid receptor binding - 0.5978 59.78%
Aromatase binding - 0.5899 58.99%
PPAR gamma + 0.6136 61.36%
Honey bee toxicity - 0.9913 99.13%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.8173 81.73%
Fish aquatic toxicity + 0.9876 98.76%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.29% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.06% 92.86%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.92% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.59% 97.29%
CHEMBL2581 P07339 Cathepsin D 86.18% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.18% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 84.12% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 82.95% 89.63%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 81.40% 85.94%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.91% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.82% 95.56%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.63% 91.81%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.33% 100.00%

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.
Cnidium monnieri

Cross-Links

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PubChem 5317016
NPASS NPC104839