Tridec-5-en-3-one

Details

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Internal ID ad54b606-ad0d-4c33-ac4d-a72cd1e8e5d2
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name (E)-tridec-5-en-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H24O/c1-3-5-6-7-8-9-10-11-12-13(14)4-2/h10-11H,3-9,12H2,1-2H3/b11-10+
InChI Key VZVCJGQVOYLQCT-ZHACJKMWSA-N
Popularity 4 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 4.50
Atomic LogP (AlogP) 4.27
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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MFCD23135584
AKOS016006261
DA-65403

2D Structure

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2D Structure of Tridec-5-en-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9477 94.77%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Plasma membrane 0.5009 50.09%
OATP2B1 inhibitior - 0.8542 85.42%
OATP1B1 inhibitior + 0.8360 83.60%
OATP1B3 inhibitior + 0.9266 92.66%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6604 66.04%
P-glycoprotein inhibitior - 0.9607 96.07%
P-glycoprotein substrate - 0.9357 93.57%
CYP3A4 substrate - 0.6220 62.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7944 79.44%
CYP3A4 inhibition - 0.9750 97.50%
CYP2C9 inhibition - 0.9462 94.62%
CYP2C19 inhibition - 0.9536 95.36%
CYP2D6 inhibition - 0.9533 95.33%
CYP1A2 inhibition + 0.7766 77.66%
CYP2C8 inhibition - 0.9057 90.57%
CYP inhibitory promiscuity - 0.7751 77.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.7313 73.13%
Eye corrosion + 0.9484 94.84%
Eye irritation + 0.9652 96.52%
Skin irritation + 0.7936 79.36%
Skin corrosion - 0.9580 95.80%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3834 38.34%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6140 61.40%
skin sensitisation + 0.9555 95.55%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5072 50.72%
Acute Oral Toxicity (c) III 0.7050 70.50%
Estrogen receptor binding - 0.8667 86.67%
Androgen receptor binding - 0.6877 68.77%
Thyroid receptor binding - 0.6832 68.32%
Glucocorticoid receptor binding - 0.5736 57.36%
Aromatase binding - 0.8859 88.59%
PPAR gamma + 0.5582 55.82%
Honey bee toxicity - 0.9901 99.01%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.8824 88.24%
Fish aquatic toxicity + 0.9185 91.85%

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 95.61% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 95.22% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.86% 92.08%
CHEMBL2581 P07339 Cathepsin D 91.80% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.48% 96.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.04% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.71% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 87.93% 85.94%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 85.85% 92.86%
CHEMBL1781 P11387 DNA topoisomerase I 85.61% 97.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.82% 89.34%
CHEMBL2885 P07451 Carbonic anhydrase III 84.14% 87.45%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.31% 91.81%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.24% 91.11%

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.
Lindera erythrocarpa
Lindera lucida

Cross-Links

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PubChem 21953547
LOTUS LTS0171767
wikiData Q104400234