Ethanone, 1-(4,5,6-trimethoxy-2-benzofuranyl)-

Details

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Internal ID 5e9c97c0-7e42-4c2b-a7ac-7dde8d248796
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 1-(4,5,6-trimethoxy-1-benzofuran-2-yl)ethanone
SMILES (Canonical) CC(=O)C1=CC2=C(C(=C(C=C2O1)OC)OC)OC
SMILES (Isomeric) CC(=O)C1=CC2=C(C(=C(C=C2O1)OC)OC)OC
InChI InChI=1S/C13H14O5/c1-7(14)9-5-8-10(18-9)6-11(15-2)13(17-4)12(8)16-3/h5-6H,1-4H3
InChI Key PBWDPQJNMGTMBI-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C13H14O5
Molecular Weight 250.25 g/mol
Exact Mass 250.08412354 g/mol
Topological Polar Surface Area (TPSA) 57.90 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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97094-18-3
Caleprunin A
DTXSID90242699

2D Structure

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2D Structure of Ethanone, 1-(4,5,6-trimethoxy-2-benzofuranyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.7599 75.99%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6225 62.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9685 96.85%
OATP1B3 inhibitior + 0.9837 98.37%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7479 74.79%
P-glycoprotein inhibitior - 0.7710 77.10%
P-glycoprotein substrate - 0.7543 75.43%
CYP3A4 substrate - 0.5564 55.64%
CYP2C9 substrate - 0.7828 78.28%
CYP2D6 substrate - 0.7575 75.75%
CYP3A4 inhibition - 0.6908 69.08%
CYP2C9 inhibition - 0.9175 91.75%
CYP2C19 inhibition + 0.6658 66.58%
CYP2D6 inhibition - 0.9220 92.20%
CYP1A2 inhibition + 0.9645 96.45%
CYP2C8 inhibition - 0.6047 60.47%
CYP inhibitory promiscuity + 0.6865 68.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4676 46.76%
Eye corrosion - 0.9255 92.55%
Eye irritation + 0.9163 91.63%
Skin irritation - 0.7571 75.71%
Skin corrosion - 0.9836 98.36%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3649 36.49%
Micronuclear + 0.7159 71.59%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.8039 80.39%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.9166 91.66%
Acute Oral Toxicity (c) II 0.6301 63.01%
Estrogen receptor binding + 0.5871 58.71%
Androgen receptor binding - 0.4844 48.44%
Thyroid receptor binding - 0.7085 70.85%
Glucocorticoid receptor binding - 0.5671 56.71%
Aromatase binding + 0.6558 65.58%
PPAR gamma - 0.5520 55.20%
Honey bee toxicity - 0.8966 89.66%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6449 64.49%
Fish aquatic toxicity + 0.9200 92.00%

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 93.19% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.63% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.28% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.59% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.91% 94.45%
CHEMBL1255126 O15151 Protein Mdm4 87.60% 90.20%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.04% 96.95%
CHEMBL2535 P11166 Glucose transporter 84.53% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.51% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.57% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.96% 89.00%

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.
Calea jamaicensis
Calea mediterranea
Calea prunifolia

Cross-Links

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PubChem 178930
LOTUS LTS0032550
wikiData Q83126507