3-(2,10-Dimethyl-11-oxododeca-1,3,5,7,9-pentaenyl)-2-methylcyclopent-2-en-1-one

Details

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Internal ID bc3b5d98-d868-4b68-a044-4bf10be0e646
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Alpha-branched alpha,beta-unsaturated ketones
IUPAC Name 3-(2,10-dimethyl-11-oxododeca-1,3,5,7,9-pentaenyl)-2-methylcyclopent-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H24O2/c1-15(14-19-12-13-20(22)17(19)3)10-8-6-5-7-9-11-16(2)18(4)21/h5-11,14H,12-13H2,1-4H3
InChI Key ZEVUZQQQWZRCFG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24O2
Molecular Weight 296.40 g/mol
Exact Mass 296.177630004 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.82
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(2,10-Dimethyl-11-oxododeca-1,3,5,7,9-pentaenyl)-2-methylcyclopent-2-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.7902 79.02%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6165 61.65%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9279 92.79%
OATP1B3 inhibitior + 0.9513 95.13%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8409 84.09%
P-glycoprotein inhibitior - 0.4883 48.83%
P-glycoprotein substrate - 0.9020 90.20%
CYP3A4 substrate - 0.5063 50.63%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8620 86.20%
CYP3A4 inhibition - 0.9311 93.11%
CYP2C9 inhibition - 0.9187 91.87%
CYP2C19 inhibition - 0.8418 84.18%
CYP2D6 inhibition - 0.8883 88.83%
CYP1A2 inhibition - 0.7563 75.63%
CYP2C8 inhibition - 0.9545 95.45%
CYP inhibitory promiscuity - 0.8762 87.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5700 57.00%
Eye corrosion - 0.8142 81.42%
Eye irritation - 0.9402 94.02%
Skin irritation + 0.7421 74.21%
Skin corrosion - 0.9021 90.21%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8775 87.75%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.6427 64.27%
skin sensitisation + 0.8004 80.04%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.5694 56.94%
Acute Oral Toxicity (c) III 0.7849 78.49%
Estrogen receptor binding + 0.8635 86.35%
Androgen receptor binding - 0.5484 54.84%
Thyroid receptor binding + 0.5711 57.11%
Glucocorticoid receptor binding - 0.6217 62.17%
Aromatase binding + 0.8008 80.08%
PPAR gamma + 0.5555 55.55%
Honey bee toxicity - 0.9198 91.98%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.6655 66.55%

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 91.11% 91.11%
CHEMBL2581 P07339 Cathepsin D 87.85% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.27% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.31% 89.34%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.26% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.11% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.88% 99.23%
CHEMBL1871 P10275 Androgen Receptor 80.35% 96.43%

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 85265516
LOTUS LTS0210233
wikiData Q105373734