Tridec-12-en-2-one

Details

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Internal ID 7bed7161-9f33-4ef5-b085-161d79f49014
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name tridec-12-en-2-one
SMILES (Canonical) CC(=O)CCCCCCCCCC=C
SMILES (Isomeric) CC(=O)CCCCCCCCCC=C
InChI InChI=1S/C13H24O/c1-3-4-5-6-7-8-9-10-11-12-13(2)14/h3H,1,4-12H2,2H3
InChI Key UYCZPLKICNDOCL-UHFFFAOYSA-N
Popularity 5 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 4.70
Atomic LogP (AlogP) 4.27
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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12-TRIDECEN-2-ONE
60437-21-0
SCHEMBL15753807
DTXSID30447222
CHEBI:186917
LMFA12000167
MFCD11553533
AKOS006324535
Q27453260

2D Structure

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2D Structure of Tridec-12-en-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.8059 80.59%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Plasma membrane 0.4642 46.42%
OATP2B1 inhibitior - 0.8508 85.08%
OATP1B1 inhibitior + 0.9487 94.87%
OATP1B3 inhibitior + 0.9114 91.14%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5451 54.51%
P-glycoprotein inhibitior - 0.9624 96.24%
P-glycoprotein substrate - 0.9641 96.41%
CYP3A4 substrate - 0.6530 65.30%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7774 77.74%
CYP3A4 inhibition - 0.9739 97.39%
CYP2C9 inhibition - 0.9389 93.89%
CYP2C19 inhibition - 0.9291 92.91%
CYP2D6 inhibition - 0.9683 96.83%
CYP1A2 inhibition + 0.6990 69.90%
CYP2C8 inhibition - 0.9697 96.97%
CYP inhibitory promiscuity - 0.8547 85.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.7045 70.45%
Eye corrosion + 0.9699 96.99%
Eye irritation + 0.9757 97.57%
Skin irritation + 0.8577 85.77%
Skin corrosion - 0.8860 88.60%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4673 46.73%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.9152 91.52%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.5639 56.39%
Acute Oral Toxicity (c) III 0.7409 74.09%
Estrogen receptor binding - 0.9013 90.13%
Androgen receptor binding - 0.9490 94.90%
Thyroid receptor binding - 0.7151 71.51%
Glucocorticoid receptor binding - 0.6366 63.66%
Aromatase binding - 0.8370 83.70%
PPAR gamma - 0.5581 55.81%
Honey bee toxicity - 0.9369 93.69%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity + 0.5124 51.24%
Fish aquatic toxicity + 0.9345 93.45%

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 93.32% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.25% 96.09%
CHEMBL1829 O15379 Histone deacetylase 3 92.97% 95.00%
CHEMBL2581 P07339 Cathepsin D 89.16% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.77% 91.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.61% 89.34%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.47% 94.33%

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.
Litsea elliptica

Cross-Links

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PubChem 10888854
LOTUS LTS0158377
wikiData Q27453260