8-Methyl-13-phenyltrideca-4,6,8,10,12-pentaen-3-one

Details

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Internal ID 73dbea3a-884c-446a-9199-777cdcaa0b65
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name 8-methyl-13-phenyltrideca-4,6,8,10,12-pentaen-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H22O/c1-3-20(21)17-11-10-13-18(2)12-6-4-7-14-19-15-8-5-9-16-19/h4-17H,3H2,1-2H3
InChI Key KMNUJIARVHVQCF-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C20H22O
Molecular Weight 278.40 g/mol
Exact Mass 278.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.29
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-Methyl-13-phenyltrideca-4,6,8,10,12-pentaen-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 + 1.0000 100.00%
Caco-2 + 0.7892 78.92%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5952 59.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8727 87.27%
OATP1B3 inhibitior + 0.9615 96.15%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8654 86.54%
P-glycoprotein inhibitior - 0.7798 77.98%
P-glycoprotein substrate - 0.8814 88.14%
CYP3A4 substrate - 0.5768 57.68%
CYP2C9 substrate - 0.7907 79.07%
CYP2D6 substrate - 0.8409 84.09%
CYP3A4 inhibition - 0.8033 80.33%
CYP2C9 inhibition - 0.8240 82.40%
CYP2C19 inhibition - 0.5731 57.31%
CYP2D6 inhibition - 0.8774 87.74%
CYP1A2 inhibition + 0.5709 57.09%
CYP2C8 inhibition - 0.5667 56.67%
CYP inhibitory promiscuity + 0.7164 71.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5181 51.81%
Carcinogenicity (trinary) Non-required 0.6308 63.08%
Eye corrosion + 0.5868 58.68%
Eye irritation + 0.6916 69.16%
Skin irritation + 0.8299 82.99%
Skin corrosion - 0.9114 91.14%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7697 76.97%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.5427 54.27%
skin sensitisation + 0.9852 98.52%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.6551 65.51%
Acute Oral Toxicity (c) III 0.8229 82.29%
Estrogen receptor binding + 0.7807 78.07%
Androgen receptor binding - 0.6785 67.85%
Thyroid receptor binding - 0.5102 51.02%
Glucocorticoid receptor binding - 0.5947 59.47%
Aromatase binding + 0.6978 69.78%
PPAR gamma + 0.5466 54.66%
Honey bee toxicity - 0.9627 96.27%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8438 84.38%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.94% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.28% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.18% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.93% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 91.63% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.57% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.51% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.21% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 86.87% 94.73%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.31% 91.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.79% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 563816
LOTUS LTS0107220
wikiData Q105143061