Tridec-2-enal

Details

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Internal ID 8fbc22de-3626-46f3-8ffb-04c47a865c3c
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name tridec-2-enal
SMILES (Canonical) CCCCCCCCCCC=CC=O
SMILES (Isomeric) CCCCCCCCCCC=CC=O
InChI InChI=1S/C13H24O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14/h11-13H,2-10H2,1H3
InChI Key VMUNAKQXJLHODT-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H24O
Molecular Weight 196.33 g/mol
Exact Mass 196.182715385 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.27
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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SCHEMBL631314
DTXSID0052883
AKOS025243566
NCI60_005309
FT-0696518

2D Structure

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2D Structure of Tridec-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 + 0.9202 92.02%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Plasma membrane 0.5260 52.60%
OATP2B1 inhibitior - 0.8552 85.52%
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 - 0.6094 60.94%
P-glycoprotein inhibitior - 0.9450 94.50%
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 + 0.9901 99.01%
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 + 0.6453 64.53%
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 - 0.7797 77.97%
Androgen receptor binding - 0.6043 60.43%
Thyroid receptor binding + 0.6726 67.26%
Glucocorticoid receptor binding - 0.6528 65.28%
Aromatase binding - 0.7198 71.98%
PPAR gamma + 0.7110 71.10%
Honey bee toxicity - 0.9842 98.42%
Biodegradation + 0.6500 65.00%
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.
Coriandrum sativum

Cross-Links

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PubChem 62653
LOTUS LTS0149552
wikiData Q105289306