Tetradec-2-enal

Details

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Internal ID 6440b9f1-d06f-4d8c-8dce-326f0c792150
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name tetradec-2-enal
SMILES (Canonical) CCCCCCCCCCCC=CC=O
SMILES (Isomeric) CCCCCCCCCCCC=CC=O
InChI InChI=1S/C14H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h12-14H,2-11H2,1H3
InChI Key WHOZNOZYMBRCBL-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C14H26O
Molecular Weight 210.36 g/mol
Exact Mass 210.198365449 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.90
Atomic LogP (AlogP) 4.66
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 11

Synonyms

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2-Tetradecenal, (2Z)-
2-tetradecen-1-al
DTXSID40199503
CHEBI:192238

2D Structure

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2D Structure of Tetradec-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 + 0.9955 99.55%
Caco-2 + 0.9192 91.92%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Plasma membrane 0.5260 52.60%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.8298 82.98%
OATP1B3 inhibitior + 0.9016 90.16%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5451 54.51%
P-glycoprotein inhibitior - 0.9406 94.06%
P-glycoprotein substrate - 0.9369 93.69%
CYP3A4 substrate - 0.6482 64.82%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8597 85.97%
CYP3A4 inhibition - 0.9911 99.11%
CYP2C9 inhibition - 0.9285 92.85%
CYP2C19 inhibition - 0.9519 95.19%
CYP2D6 inhibition - 0.9653 96.53%
CYP1A2 inhibition + 0.7244 72.44%
CYP2C8 inhibition - 0.9364 93.64%
CYP inhibitory promiscuity - 0.7617 76.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6467 64.67%
Eye corrosion + 0.9927 99.27%
Eye irritation + 0.9850 98.50%
Skin irritation + 0.9187 91.87%
Skin corrosion - 0.8516 85.16%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3638 36.38%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5059 50.59%
skin sensitisation + 0.9648 96.48%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.9954 99.54%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5841 58.41%
Acute Oral Toxicity (c) III 0.8135 81.35%
Estrogen receptor binding - 0.6359 63.59%
Androgen receptor binding - 0.6043 60.43%
Thyroid receptor binding + 0.7831 78.31%
Glucocorticoid receptor binding - 0.5693 56.93%
Aromatase binding - 0.6444 64.44%
PPAR gamma + 0.7475 74.75%
Honey bee toxicity - 0.9842 98.42%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity + 0.9253 92.53%
Fish aquatic toxicity + 0.9804 98.04%

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 94.99% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 94.61% 89.63%
CHEMBL2581 P07339 Cathepsin D 92.24% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.72% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.73% 92.86%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.46% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.41% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.30% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.79% 91.81%
CHEMBL1781 P11387 DNA topoisomerase I 83.46% 97.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.42% 89.34%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.04% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 81.00% 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.
Citrus maxima
Leonurus japonicus

Cross-Links

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PubChem 116625
NPASS NPC244369
LOTUS LTS0177671
wikiData Q81997276