Methyl 2-(7-hydroxy-2-methyl-3-oxo-1-benzofuran-2-yl)acetate

Details

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Internal ID f6af313d-8e53-4356-869c-fdbe4c53d964
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name methyl 2-(7-hydroxy-2-methyl-3-oxo-1-benzofuran-2-yl)acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H12O5/c1-12(6-9(14)16-2)11(15)7-4-3-5-8(13)10(7)17-12/h3-5,13H,6H2,1-2H3
InChI Key YTPUQMXLGHNLPS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H12O5
Molecular Weight 236.22 g/mol
Exact Mass 236.06847348 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.29
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 2-(7-hydroxy-2-methyl-3-oxo-1-benzofuran-2-yl)acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9847 98.47%
Caco-2 + 0.7560 75.60%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.6826 68.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8806 88.06%
OATP1B3 inhibitior + 0.9018 90.18%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8647 86.47%
P-glycoprotein inhibitior - 0.9671 96.71%
P-glycoprotein substrate - 0.7590 75.90%
CYP3A4 substrate + 0.5611 56.11%
CYP2C9 substrate - 0.5799 57.99%
CYP2D6 substrate - 0.7993 79.93%
CYP3A4 inhibition - 0.8220 82.20%
CYP2C9 inhibition - 0.8740 87.40%
CYP2C19 inhibition - 0.9298 92.98%
CYP2D6 inhibition - 0.9280 92.80%
CYP1A2 inhibition - 0.7720 77.20%
CYP2C8 inhibition - 0.6684 66.84%
CYP inhibitory promiscuity - 0.9119 91.19%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5337 53.37%
Eye corrosion - 0.9716 97.16%
Eye irritation + 0.5513 55.13%
Skin irritation - 0.7171 71.71%
Skin corrosion - 0.9089 90.89%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7419 74.19%
Micronuclear - 0.5941 59.41%
Hepatotoxicity - 0.6064 60.64%
skin sensitisation - 0.7372 73.72%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.8054 80.54%
Acute Oral Toxicity (c) III 0.4762 47.62%
Estrogen receptor binding - 0.7206 72.06%
Androgen receptor binding - 0.5159 51.59%
Thyroid receptor binding - 0.7110 71.10%
Glucocorticoid receptor binding - 0.6214 62.14%
Aromatase binding - 0.6232 62.32%
PPAR gamma - 0.7878 78.78%
Honey bee toxicity - 0.9181 91.81%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9480 94.80%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.45% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.09% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.19% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 92.63% 83.82%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.50% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 88.53% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.52% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.97% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.76% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.14% 94.00%
CHEMBL1951 P21397 Monoamine oxidase A 81.90% 91.49%
CHEMBL2535 P11166 Glucose transporter 81.81% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.94% 99.17%
CHEMBL4208 P20618 Proteasome component C5 80.18% 90.00%

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.
Dionaea muscipula

Cross-Links

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PubChem 163020396
LOTUS LTS0271847
wikiData Q105350352