(7Z,10Z)-2,7,9,9-tetramethylcycloundeca-7,10-diene-1,6-dione

Details

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Internal ID eb2db09e-5377-4f09-bd5e-d130b19b082b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name (7Z,10Z)-2,7,9,9-tetramethylcycloundeca-7,10-diene-1,6-dione
SMILES (Canonical) CC1CCCC(=O)C(=CC(C=CC1=O)(C)C)C
SMILES (Isomeric) CC1CCCC(=O)/C(=C\C(/C=C\C1=O)(C)C)/C
InChI InChI=1S/C15H22O2/c1-11-6-5-7-13(16)12(2)10-15(3,4)9-8-14(11)17/h8-11H,5-7H2,1-4H3/b9-8-,12-10-
InChI Key NFDDZSDTJCSOCJ-DMGFJBLZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.47
H-Bond Acceptor 2
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 (7Z,10Z)-2,7,9,9-tetramethylcycloundeca-7,10-diene-1,6-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.8838 88.38%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5836 58.36%
OATP2B1 inhibitior - 0.8534 85.34%
OATP1B1 inhibitior + 0.8998 89.98%
OATP1B3 inhibitior + 0.9266 92.66%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7047 70.47%
P-glycoprotein inhibitior - 0.9605 96.05%
P-glycoprotein substrate - 0.8743 87.43%
CYP3A4 substrate + 0.5483 54.83%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8706 87.06%
CYP3A4 inhibition - 0.8287 82.87%
CYP2C9 inhibition - 0.8739 87.39%
CYP2C19 inhibition - 0.7858 78.58%
CYP2D6 inhibition - 0.8986 89.86%
CYP1A2 inhibition - 0.7044 70.44%
CYP2C8 inhibition - 0.9114 91.14%
CYP inhibitory promiscuity - 0.8775 87.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5123 51.23%
Eye corrosion - 0.9250 92.50%
Eye irritation + 0.5677 56.77%
Skin irritation + 0.6710 67.10%
Skin corrosion - 0.9277 92.77%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4091 40.91%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation + 0.9081 90.81%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.5523 55.23%
Acute Oral Toxicity (c) III 0.7501 75.01%
Estrogen receptor binding - 0.9366 93.66%
Androgen receptor binding - 0.8037 80.37%
Thyroid receptor binding - 0.6915 69.15%
Glucocorticoid receptor binding - 0.8406 84.06%
Aromatase binding - 0.7979 79.79%
PPAR gamma - 0.7474 74.74%
Honey bee toxicity - 0.9363 93.63%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.8542 85.42%

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 92.07% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 89.05% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.65% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.90% 97.25%
CHEMBL2581 P07339 Cathepsin D 87.32% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.58% 93.04%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.12% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.07% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.40% 97.09%
CHEMBL3012 Q13946 Phosphodiesterase 7A 83.60% 99.29%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.51% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.85% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.43% 93.99%

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 100951544
LOTUS LTS0246733
wikiData Q105178382