3-(Furan-3-yl)-6-hydroxy-3a,7-dimethyl-3,4,5,6-tetrahydro-2-benzofuran-1-one

Details

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Internal ID 39980b84-0ffd-49c3-8104-e3607f089d6b
Taxonomy Organoheterocyclic compounds > Isobenzofurans
IUPAC Name 3-(furan-3-yl)-6-hydroxy-3a,7-dimethyl-3,4,5,6-tetrahydro-2-benzofuran-1-one
SMILES (Canonical) CC1=C2C(=O)OC(C2(CCC1O)C)C3=COC=C3
SMILES (Isomeric) CC1=C2C(=O)OC(C2(CCC1O)C)C3=COC=C3
InChI InChI=1S/C14H16O4/c1-8-10(15)3-5-14(2)11(8)13(16)18-12(14)9-4-6-17-7-9/h4,6-7,10,12,15H,3,5H2,1-2H3
InChI Key ZCEUBPHEBYXFLM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16O4
Molecular Weight 248.27 g/mol
Exact Mass 248.10485899 g/mol
Topological Polar Surface Area (TPSA) 59.70 Ų
XlogP 1.20
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(Furan-3-yl)-6-hydroxy-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 + 0.9968 99.68%
Caco-2 + 0.6704 67.04%
Blood Brain Barrier + 0.6355 63.55%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7387 73.87%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.6865 68.65%
OATP1B3 inhibitior + 0.9140 91.40%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9339 93.39%
P-glycoprotein inhibitior - 0.9471 94.71%
P-glycoprotein substrate - 0.8864 88.64%
CYP3A4 substrate + 0.5618 56.18%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8567 85.67%
CYP3A4 inhibition - 0.6129 61.29%
CYP2C9 inhibition - 0.8418 84.18%
CYP2C19 inhibition - 0.9003 90.03%
CYP2D6 inhibition - 0.9296 92.96%
CYP1A2 inhibition - 0.6236 62.36%
CYP2C8 inhibition - 0.7384 73.84%
CYP inhibitory promiscuity - 0.8859 88.59%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.3974 39.74%
Eye corrosion - 0.9878 98.78%
Eye irritation - 0.9344 93.44%
Skin irritation - 0.5195 51.95%
Skin corrosion - 0.8087 80.87%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4133 41.33%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.7180 71.80%
skin sensitisation - 0.7541 75.41%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.6955 69.55%
Acute Oral Toxicity (c) II 0.3956 39.56%
Estrogen receptor binding - 0.6260 62.60%
Androgen receptor binding - 0.5940 59.40%
Thyroid receptor binding - 0.5660 56.60%
Glucocorticoid receptor binding - 0.7150 71.50%
Aromatase binding - 0.6167 61.67%
PPAR gamma + 0.5292 52.92%
Honey bee toxicity - 0.9569 95.69%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9670 96.70%

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 93.35% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.23% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.43% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.36% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.65% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.60% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.40% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.27% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.85% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.33% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.01% 100.00%
CHEMBL3038469 P24941 CDK2/Cyclin A 81.94% 91.38%
CHEMBL221 P23219 Cyclooxygenase-1 81.85% 90.17%

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
Melia azedarach

Cross-Links

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PubChem 14543429
LOTUS LTS0156663
wikiData Q105371059