(3S,3aR)-3-(furan-3-yl)-3a,7-dimethyl-3,4,5,6-tetrahydro-2-benzofuran-1-one

Details

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Internal ID 7a564161-b6f6-4632-b278-2101c4909d14
Taxonomy Organoheterocyclic compounds > Isobenzofurans
IUPAC Name (3S,3aR)-3-(furan-3-yl)-3a,7-dimethyl-3,4,5,6-tetrahydro-2-benzofuran-1-one
SMILES (Canonical) CC1=C2C(=O)OC(C2(CCC1)C)C3=COC=C3
SMILES (Isomeric) CC1=C2C(=O)O[C@@H]([C@@]2(CCC1)C)C3=COC=C3
InChI InChI=1S/C14H16O3/c1-9-4-3-6-14(2)11(9)13(15)17-12(14)10-5-7-16-8-10/h5,7-8,12H,3-4,6H2,1-2H3/t12-,14-/m1/s1
InChI Key XYYAFLHHHZVPRN-TZMCWYRMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16O3
Molecular Weight 232.27 g/mol
Exact Mass 232.109944368 g/mol
Topological Polar Surface Area (TPSA) 39.40 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.38
H-Bond Acceptor 3
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 (3S,3aR)-3-(furan-3-yl)-3a,7-dimethyl-3,4,5,6-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 + 0.8656 86.56%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6361 63.61%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.7207 72.07%
OATP1B3 inhibitior + 0.9391 93.91%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.8510 85.10%
P-glycoprotein inhibitior - 0.9560 95.60%
P-glycoprotein substrate - 0.9238 92.38%
CYP3A4 substrate + 0.5512 55.12%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8734 87.34%
CYP3A4 inhibition - 0.6174 61.74%
CYP2C9 inhibition - 0.8126 81.26%
CYP2C19 inhibition - 0.7527 75.27%
CYP2D6 inhibition - 0.9115 91.15%
CYP1A2 inhibition + 0.7521 75.21%
CYP2C8 inhibition - 0.7553 75.53%
CYP inhibitory promiscuity - 0.5861 58.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.4420 44.20%
Eye corrosion - 0.9762 97.62%
Eye irritation - 0.9617 96.17%
Skin irritation - 0.5379 53.79%
Skin corrosion - 0.8682 86.82%
Ames mutagenesis - 0.6407 64.07%
Human Ether-a-go-go-Related Gene inhibition + 0.6419 64.19%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.5983 59.83%
skin sensitisation - 0.6483 64.83%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.5966 59.66%
Acute Oral Toxicity (c) II 0.7151 71.51%
Estrogen receptor binding - 0.5938 59.38%
Androgen receptor binding - 0.5869 58.69%
Thyroid receptor binding - 0.5561 55.61%
Glucocorticoid receptor binding - 0.8140 81.40%
Aromatase binding - 0.5376 53.76%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.9458 94.58%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9945 99.45%

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 93.79% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.64% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.24% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.16% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.98% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.37% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.17% 97.09%
CHEMBL3038469 P24941 CDK2/Cyclin A 83.66% 91.38%
CHEMBL3401 O75469 Pregnane X receptor 83.08% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.99% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.31% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.09% 95.89%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.23% 93.04%

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.
Aesculus hippocastanum
Chimonanthus praecox
Dictamnus dasycarpus
Fraxinus chinensis subsp. chinensis
Fraxinus ornus
Fraxinus stylosa
Melia azedarach

Cross-Links

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PubChem 776141
NPASS NPC265656