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

Details

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Internal ID 389348d2-17d0-43c8-a85f-5ad500f7bf8a
Taxonomy Organoheterocyclic compounds > Isobenzofurans
IUPAC Name (3R,3aR)-3-(furan-3-yl)-3a,7-dimethyl-3,4,5,7a-tetrahydro-2-benzofuran-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H16O3/c1-9-4-3-6-14(2)11(9)13(15)17-12(14)10-5-7-16-8-10/h4-5,7-8,11-12H,3,6H2,1-2H3/t11?,12-,14+/m0/s1
InChI Key CKJJQJLXFWVISP-VBVNFKHJSA-N
Popularity 3 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 2.20
Atomic LogP (AlogP) 3.24
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 (3R,3aR)-3-(furan-3-yl)-3a,7-dimethyl-3,4,5,7a-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 + 0.7957 79.57%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6057 60.57%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8182 81.82%
OATP1B3 inhibitior + 0.9241 92.41%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9390 93.90%
P-glycoprotein inhibitior - 0.9444 94.44%
P-glycoprotein substrate - 0.8587 85.87%
CYP3A4 substrate + 0.5633 56.33%
CYP2C9 substrate - 0.7919 79.19%
CYP2D6 substrate - 0.8265 82.65%
CYP3A4 inhibition - 0.5923 59.23%
CYP2C9 inhibition - 0.8219 82.19%
CYP2C19 inhibition - 0.7679 76.79%
CYP2D6 inhibition - 0.9109 91.09%
CYP1A2 inhibition + 0.7656 76.56%
CYP2C8 inhibition - 0.7224 72.24%
CYP inhibitory promiscuity - 0.5171 51.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4163 41.63%
Eye corrosion - 0.9752 97.52%
Eye irritation - 0.9561 95.61%
Skin irritation + 0.4909 49.09%
Skin corrosion - 0.7906 79.06%
Ames mutagenesis - 0.7370 73.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4153 41.53%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.5158 51.58%
skin sensitisation - 0.5885 58.85%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5449 54.49%
Acute Oral Toxicity (c) II 0.5510 55.10%
Estrogen receptor binding - 0.6136 61.36%
Androgen receptor binding - 0.5376 53.76%
Thyroid receptor binding - 0.6358 63.58%
Glucocorticoid receptor binding - 0.7877 78.77%
Aromatase binding - 0.6322 63.22%
PPAR gamma - 0.5467 54.67%
Honey bee toxicity - 0.9016 90.16%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9880 98.80%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 90.91% 97.09%
CHEMBL1951 P21397 Monoamine oxidase A 90.71% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.32% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.94% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.29% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.01% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.05% 89.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.69% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.36% 86.33%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.19% 100.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.71% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 81.80% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.76% 99.23%

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.
Dictamnus dasycarpus
Fagaropsis glabra

Cross-Links

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PubChem 101922291
LOTUS LTS0270323
wikiData Q104396452