(2E,4E)-2-tridecylheptadeca-2,4-dienal

Details

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Internal ID ae6a3087-9013-47ab-91fd-39911cc45f83
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name (2E,4E)-2-tridecylheptadeca-2,4-dienal
SMILES (Canonical) CCCCCCCCCCCCCC(=CC=CCCCCCCCCCCCC)C=O
SMILES (Isomeric) CCCCCCCCCCCCC/C(=C\C=C\CCCCCCCCCCCC)/C=O
InChI InChI=1S/C30H56O/c1-3-5-7-9-11-13-15-16-18-20-22-24-26-28-30(29-31)27-25-23-21-19-17-14-12-10-8-6-4-2/h24,26,28-29H,3-23,25,27H2,1-2H3/b26-24+,30-28+
InChI Key UBNBPKYIOQKKCQ-GASNPIGISA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H56O
Molecular Weight 432.80 g/mol
Exact Mass 432.433116406 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 13.80
Atomic LogP (AlogP) 10.68
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 25

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,4E)-2-tridecylheptadeca-2,4-dienal

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 - 0.5785 57.85%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Lysosomes 0.3038 30.38%
OATP2B1 inhibitior - 0.8549 85.49%
OATP1B1 inhibitior + 0.7551 75.51%
OATP1B3 inhibitior + 0.9267 92.67%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.7926 79.26%
P-glycoprotein inhibitior - 0.4835 48.35%
P-glycoprotein substrate - 0.8859 88.59%
CYP3A4 substrate - 0.5533 55.33%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.8302 83.02%
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 - 0.8836 88.36%
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 + 0.8084 80.84%
Skin irritation + 0.8111 81.11%
Skin corrosion - 0.8916 89.16%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6527 65.27%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5045 50.45%
skin sensitisation + 0.9652 96.52%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity - 0.5735 57.35%
Acute Oral Toxicity (c) III 0.8186 81.86%
Estrogen receptor binding + 0.6011 60.11%
Androgen receptor binding - 0.6367 63.67%
Thyroid receptor binding + 0.6293 62.93%
Glucocorticoid receptor binding - 0.7155 71.55%
Aromatase binding - 0.5561 55.61%
PPAR gamma + 0.5954 59.54%
Honey bee toxicity - 0.9836 98.36%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.8806 88.06%
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
CHEMBL3060 Q9Y345 Glycine transporter 2 96.50% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 95.76% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.06% 92.08%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 93.52% 85.94%
CHEMBL2581 P07339 Cathepsin D 93.23% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.75% 97.29%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 87.72% 92.86%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.24% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.84% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 82.64% 94.73%
CHEMBL1781 P11387 DNA topoisomerase I 82.53% 97.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.83% 95.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.62% 100.00%
CHEMBL299 P17252 Protein kinase C alpha 80.89% 98.03%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.37% 91.81%

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.
Equisetum hyemale

Cross-Links

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PubChem 21773677
NPASS NPC176426
LOTUS LTS0218838
wikiData Q105269501