2-(6-Acetyl-5-hydroxy-1-benzofuran-2-yl)prop-2-enyl acetate

Details

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Internal ID a196431e-7c9a-4612-beaf-55ac1fe1d17b
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 2-(6-acetyl-5-hydroxy-1-benzofuran-2-yl)prop-2-enyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H14O5/c1-8(7-19-10(3)17)14-5-11-4-13(18)12(9(2)16)6-15(11)20-14/h4-6,18H,1,7H2,2-3H3
InChI Key WKTBMSBPLSKSKZ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H14O5
Molecular Weight 274.27 g/mol
Exact Mass 274.08412354 g/mol
Topological Polar Surface Area (TPSA) 76.70 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.92
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(6-Acetyl-5-hydroxy-1-benzofuran-2-yl)prop-2-enyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.5104 51.04%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7734 77.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9083 90.83%
OATP1B3 inhibitior + 0.9244 92.44%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7121 71.21%
P-glycoprotein inhibitior - 0.7491 74.91%
P-glycoprotein substrate - 0.6993 69.93%
CYP3A4 substrate - 0.5448 54.48%
CYP2C9 substrate + 0.6101 61.01%
CYP2D6 substrate - 0.8855 88.55%
CYP3A4 inhibition - 0.6455 64.55%
CYP2C9 inhibition + 0.7186 71.86%
CYP2C19 inhibition + 0.7522 75.22%
CYP2D6 inhibition - 0.9036 90.36%
CYP1A2 inhibition + 0.8761 87.61%
CYP2C8 inhibition - 0.6387 63.87%
CYP inhibitory promiscuity + 0.6508 65.08%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9240 92.40%
Carcinogenicity (trinary) Non-required 0.6816 68.16%
Eye corrosion - 0.9804 98.04%
Eye irritation - 0.5614 56.14%
Skin irritation - 0.7099 70.99%
Skin corrosion - 0.9464 94.64%
Ames mutagenesis - 0.6054 60.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6955 69.55%
Micronuclear + 0.5333 53.33%
Hepatotoxicity + 0.5060 50.60%
skin sensitisation - 0.5440 54.40%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.7033 70.33%
Acute Oral Toxicity (c) III 0.4180 41.80%
Estrogen receptor binding + 0.7440 74.40%
Androgen receptor binding - 0.5194 51.94%
Thyroid receptor binding - 0.7024 70.24%
Glucocorticoid receptor binding + 0.6522 65.22%
Aromatase binding + 0.7693 76.93%
PPAR gamma + 0.5927 59.27%
Honey bee toxicity - 0.8800 88.00%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6950 69.50%
Fish aquatic toxicity + 1.0000 100.00%

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 98.13% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 92.07% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.66% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.34% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.70% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.41% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.70% 86.33%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 88.70% 94.42%
CHEMBL4040 P28482 MAP kinase ERK2 85.80% 83.82%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.81% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.12% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.52% 85.14%
CHEMBL4581 P52732 Kinesin-like protein 1 80.03% 93.18%

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.
Eupatorium cannabinum

Cross-Links

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PubChem 85775718
NPASS NPC93803
LOTUS LTS0159066
wikiData Q105307669