4,4,8-Trimethylcycloundeca-2,8-dien-1-one

Details

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Internal ID 30a05c85-a774-484c-a156-0831ce694d9b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 4,4,8-trimethylcycloundeca-2,8-dien-1-one
SMILES (Canonical) CC1=CCCC(=O)C=CC(CCC1)(C)C
SMILES (Isomeric) CC1=CCCC(=O)C=CC(CCC1)(C)C
InChI InChI=1S/C14H22O/c1-12-6-4-8-13(15)9-11-14(2,3)10-5-7-12/h6,9,11H,4-5,7-8,10H2,1-3H3
InChI Key DSPDFJOUMGPCOG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22O
Molecular Weight 206.32 g/mol
Exact Mass 206.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.05
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,4,8-Trimethylcycloundeca-2,8-dien-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 + 0.9959 99.59%
Caco-2 + 0.9809 98.09%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.4807 48.07%
OATP2B1 inhibitior - 0.8461 84.61%
OATP1B1 inhibitior + 0.9372 93.72%
OATP1B3 inhibitior + 0.9577 95.77%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.9477 94.77%
P-glycoprotein substrate - 0.9682 96.82%
CYP3A4 substrate - 0.5258 52.58%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8610 86.10%
CYP3A4 inhibition - 0.8995 89.95%
CYP2C9 inhibition - 0.8138 81.38%
CYP2C19 inhibition - 0.7752 77.52%
CYP2D6 inhibition - 0.9487 94.87%
CYP1A2 inhibition - 0.7169 71.69%
CYP2C8 inhibition - 0.9503 95.03%
CYP inhibitory promiscuity - 0.9042 90.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.4989 49.89%
Eye corrosion - 0.8236 82.36%
Eye irritation + 0.8924 89.24%
Skin irritation + 0.7282 72.82%
Skin corrosion - 0.9725 97.25%
Ames mutagenesis - 0.8034 80.34%
Human Ether-a-go-go-Related Gene inhibition - 0.6458 64.58%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5140 51.40%
skin sensitisation + 0.9167 91.67%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5858 58.58%
Acute Oral Toxicity (c) III 0.6930 69.30%
Estrogen receptor binding - 0.9448 94.48%
Androgen receptor binding - 0.8815 88.15%
Thyroid receptor binding - 0.8044 80.44%
Glucocorticoid receptor binding - 0.7950 79.50%
Aromatase binding - 0.7842 78.42%
PPAR gamma - 0.7734 77.34%
Honey bee toxicity - 0.9479 94.79%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9366 93.66%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.64% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.09% 91.11%
CHEMBL2581 P07339 Cathepsin D 87.21% 98.95%
CHEMBL4208 P20618 Proteasome component C5 85.36% 90.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.21% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.45% 97.25%

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.
Blainvillea acmella
Mikania alvimii
Rudbeckia laciniata

Cross-Links

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PubChem 85975255
LOTUS LTS0020487
wikiData Q104987941