(2R)-2,6-dihydroxy-2,4-dimethyl-1-benzofuran-3-one

Details

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Internal ID 22c9bf20-a65e-4953-8df6-cc7477b5b40b
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name (2R)-2,6-dihydroxy-2,4-dimethyl-1-benzofuran-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H10O4/c1-5-3-6(11)4-7-8(5)9(12)10(2,13)14-7/h3-4,11,13H,1-2H3/t10-/m1/s1
InChI Key ZNVGYHOBTCWGTO-SNVBAGLBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O4
Molecular Weight 194.18 g/mol
Exact Mass 194.05790880 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.98
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R)-2,6-dihydroxy-2,4-dimethyl-1-benzofuran-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9668 96.68%
Caco-2 + 0.5404 54.04%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7516 75.16%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9014 90.14%
OATP1B3 inhibitior + 0.8903 89.03%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9550 95.50%
P-glycoprotein inhibitior - 0.9613 96.13%
P-glycoprotein substrate - 0.9685 96.85%
CYP3A4 substrate - 0.5150 51.50%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8380 83.80%
CYP3A4 inhibition - 0.8276 82.76%
CYP2C9 inhibition - 0.8229 82.29%
CYP2C19 inhibition - 0.8104 81.04%
CYP2D6 inhibition - 0.9485 94.85%
CYP1A2 inhibition + 0.5532 55.32%
CYP2C8 inhibition - 0.7200 72.00%
CYP inhibitory promiscuity - 0.7605 76.05%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5379 53.79%
Eye corrosion - 0.9201 92.01%
Eye irritation + 0.9181 91.81%
Skin irritation + 0.5861 58.61%
Skin corrosion - 0.9014 90.14%
Ames mutagenesis - 0.7770 77.70%
Human Ether-a-go-go-Related Gene inhibition - 0.7349 73.49%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.5177 51.77%
skin sensitisation - 0.6686 66.86%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.7870 78.70%
Acute Oral Toxicity (c) III 0.4508 45.08%
Estrogen receptor binding - 0.5613 56.13%
Androgen receptor binding - 0.5687 56.87%
Thyroid receptor binding - 0.5633 56.33%
Glucocorticoid receptor binding - 0.7104 71.04%
Aromatase binding - 0.6769 67.69%
PPAR gamma - 0.7743 77.43%
Honey bee toxicity - 0.9425 94.25%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9263 92.63%

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 97.67% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.01% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.91% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.27% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 87.26% 94.73%
CHEMBL4208 P20618 Proteasome component C5 86.64% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.91% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.33% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.89% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.32% 99.23%
CHEMBL4040 P28482 MAP kinase ERK2 81.03% 83.82%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.02% 94.80%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.06% 94.00%

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.
Sideritis soluta

Cross-Links

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PubChem 163015876
LOTUS LTS0151898
wikiData Q105380244