1-(3,5-Dimethyl-1-benzofuran-6-yl)pentane-1,4-dione

Details

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Internal ID edccb3b5-34eb-47cd-974a-b0c37cb8143d
Taxonomy Benzenoids > Benzene and substituted derivatives > Butyrophenones
IUPAC Name 1-(3,5-dimethyl-1-benzofuran-6-yl)pentane-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O3/c1-9-6-13-10(2)8-18-15(13)7-12(9)14(17)5-4-11(3)16/h6-8H,4-5H2,1-3H3
InChI Key BIQIXQNJOKXALH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O3
Molecular Weight 244.28 g/mol
Exact Mass 244.109944368 g/mol
Topological Polar Surface Area (TPSA) 47.30 Ų
XlogP 2.30
Atomic LogP (AlogP) 3.60
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(3,5-Dimethyl-1-benzofuran-6-yl)pentane-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.8952 89.52%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6280 62.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9240 92.40%
OATP1B3 inhibitior + 0.9626 96.26%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5663 56.63%
P-glycoprotein inhibitior - 0.8896 88.96%
P-glycoprotein substrate - 0.8852 88.52%
CYP3A4 substrate - 0.5933 59.33%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.7985 79.85%
CYP3A4 inhibition - 0.9108 91.08%
CYP2C9 inhibition - 0.7877 78.77%
CYP2C19 inhibition - 0.7557 75.57%
CYP2D6 inhibition - 0.9481 94.81%
CYP1A2 inhibition + 0.7588 75.88%
CYP2C8 inhibition - 0.6899 68.99%
CYP inhibitory promiscuity - 0.7081 70.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.5865 58.65%
Eye corrosion - 0.9721 97.21%
Eye irritation - 0.8594 85.94%
Skin irritation - 0.6179 61.79%
Skin corrosion - 0.8864 88.64%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5177 51.77%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.6681 66.81%
skin sensitisation + 0.5437 54.37%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.7339 73.39%
Acute Oral Toxicity (c) III 0.6408 64.08%
Estrogen receptor binding - 0.5173 51.73%
Androgen receptor binding - 0.7311 73.11%
Thyroid receptor binding - 0.7686 76.86%
Glucocorticoid receptor binding + 0.5502 55.02%
Aromatase binding - 0.5812 58.12%
PPAR gamma - 0.5734 57.34%
Honey bee toxicity - 0.9401 94.01%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9550 95.50%

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 93.99% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 89.48% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.48% 89.00%
CHEMBL2581 P07339 Cathepsin D 85.73% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.68% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.45% 99.17%
CHEMBL4208 P20618 Proteasome component C5 81.57% 90.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.47% 93.65%

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.
Euryops jacksonii

Cross-Links

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PubChem 14890358
LOTUS LTS0267045
wikiData Q104936708