(2Z,6Z)-4,4,7,11-tetramethylcycloundeca-2,6-dien-1-one

Details

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Internal ID e1822a87-8e85-4764-9040-89fdb9d104f5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2Z,6Z)-4,4,7,11-tetramethylcycloundeca-2,6-dien-1-one
SMILES (Canonical) CC1CCCC(=CCC(C=CC1=O)(C)C)C
SMILES (Isomeric) CC1CCC/C(=C\CC(/C=C\C1=O)(C)C)/C
InChI InChI=1S/C15H24O/c1-12-6-5-7-13(2)14(16)9-11-15(3,4)10-8-12/h8-9,11,13H,5-7,10H2,1-4H3/b11-9-,12-8-
InChI Key AVAUYZGSANWIET-WBWBCYDVSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.29
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 (2Z,6Z)-4,4,7,11-tetramethylcycloundeca-2,6-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 + 0.9961 99.61%
Caco-2 + 0.9350 93.50%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.4522 45.22%
OATP2B1 inhibitior - 0.8473 84.73%
OATP1B1 inhibitior + 0.9198 91.98%
OATP1B3 inhibitior + 0.8882 88.82%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.6842 68.42%
P-glycoprotein inhibitior - 0.9509 95.09%
P-glycoprotein substrate - 0.9011 90.11%
CYP3A4 substrate + 0.5638 56.38%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8706 87.06%
CYP3A4 inhibition - 0.9226 92.26%
CYP2C9 inhibition - 0.8155 81.55%
CYP2C19 inhibition - 0.7701 77.01%
CYP2D6 inhibition - 0.9448 94.48%
CYP1A2 inhibition - 0.6719 67.19%
CYP2C8 inhibition - 0.9124 91.24%
CYP inhibitory promiscuity - 0.8191 81.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5159 51.59%
Eye corrosion - 0.8938 89.38%
Eye irritation + 0.8407 84.07%
Skin irritation + 0.6905 69.05%
Skin corrosion - 0.9745 97.45%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4598 45.98%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.9082 90.82%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.6314 63.14%
Acute Oral Toxicity (c) III 0.6020 60.20%
Estrogen receptor binding - 0.9420 94.20%
Androgen receptor binding - 0.7940 79.40%
Thyroid receptor binding - 0.7068 70.68%
Glucocorticoid receptor binding - 0.8318 83.18%
Aromatase binding - 0.7353 73.53%
PPAR gamma - 0.7957 79.57%
Honey bee toxicity - 0.9392 93.92%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9848 98.48%

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 92.93% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.74% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 88.80% 86.00%
CHEMBL2581 P07339 Cathepsin D 87.91% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.96% 97.25%
CHEMBL1871 P10275 Androgen Receptor 86.38% 96.43%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.15% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.64% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.94% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.44% 92.94%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.27% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.47% 95.89%

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.
Buddleja globosa

Cross-Links

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PubChem 100951543
LOTUS LTS0009873
wikiData Q104919280