7-Ethylidene-6-(1,3,3-trimethylcyclohexyl)-3,3a,4,7a-tetrahydro-2-benzofuran-1-one

Details

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Internal ID 9134b1bc-692e-41a7-9f29-3a5293099169
Taxonomy Organoheterocyclic compounds > Isobenzofurans
IUPAC Name 7-ethylidene-6-(1,3,3-trimethylcyclohexyl)-3,3a,4,7a-tetrahydro-2-benzofuran-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H28O2/c1-5-14-15(8-7-13-11-21-17(20)16(13)14)19(4)10-6-9-18(2,3)12-19/h5,8,13,16H,6-7,9-12H2,1-4H3
InChI Key JYGCZJWYAJTITQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H28O2
Molecular Weight 288.40 g/mol
Exact Mass 288.208930132 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.66
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Ethylidene-6-(1,3,3-trimethylcyclohexyl)-3,3a,4,7a-tetrahydro-2-benzofuran-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 + 1.0000 100.00%
Caco-2 + 0.7919 79.19%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6526 65.26%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.8921 89.21%
OATP1B3 inhibitior + 0.9142 91.42%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.7304 73.04%
P-glycoprotein inhibitior - 0.8192 81.92%
P-glycoprotein substrate - 0.7665 76.65%
CYP3A4 substrate + 0.5977 59.77%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8739 87.39%
CYP3A4 inhibition - 0.8483 84.83%
CYP2C9 inhibition - 0.8023 80.23%
CYP2C19 inhibition + 0.6339 63.39%
CYP2D6 inhibition - 0.9051 90.51%
CYP1A2 inhibition - 0.6403 64.03%
CYP2C8 inhibition - 0.7362 73.62%
CYP inhibitory promiscuity - 0.6437 64.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5324 53.24%
Eye corrosion - 0.9792 97.92%
Eye irritation - 0.9076 90.76%
Skin irritation - 0.6694 66.94%
Skin corrosion - 0.9611 96.11%
Ames mutagenesis - 0.5137 51.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7193 71.93%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.5178 51.78%
skin sensitisation - 0.6315 63.15%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.7429 74.29%
Acute Oral Toxicity (c) III 0.6246 62.46%
Estrogen receptor binding + 0.5450 54.50%
Androgen receptor binding + 0.8101 81.01%
Thyroid receptor binding + 0.5979 59.79%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.6992 69.92%
PPAR gamma - 0.5905 59.05%
Honey bee toxicity - 0.8079 80.79%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 1.0000 100.00%

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 95.55% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.16% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.97% 95.56%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 90.26% 83.57%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.76% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.69% 89.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.49% 96.61%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.14% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.14% 95.89%
CHEMBL2581 P07339 Cathepsin D 86.67% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.47% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.36% 82.69%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.68% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 81.23% 94.75%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.07% 96.77%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.01% 94.80%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.67% 86.33%

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 72738631
LOTUS LTS0005374
wikiData Q105136986