Methyl 3-(6-hydroxy-1-benzofuran-5-yl)propanoate

Details

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Internal ID 9c27cdbb-1665-43f0-b0bb-d1918458a06c
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name methyl 3-(6-hydroxy-1-benzofuran-5-yl)propanoate
SMILES (Canonical) COC(=O)CCC1=C(C=C2C(=C1)C=CO2)O
SMILES (Isomeric) COC(=O)CCC1=C(C=C2C(=C1)C=CO2)O
InChI InChI=1S/C12H12O4/c1-15-12(14)3-2-8-6-9-4-5-16-11(9)7-10(8)13/h4-7,13H,2-3H2,1H3
InChI Key NLTUVCNZNQAURV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H12O4
Molecular Weight 220.22 g/mol
Exact Mass 220.07355886 g/mol
Topological Polar Surface Area (TPSA) 59.70 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.24
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 3-(6-hydroxy-1-benzofuran-5-yl)propanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9851 98.51%
Caco-2 + 0.7374 73.74%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7624 76.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9274 92.74%
OATP1B3 inhibitior + 0.9394 93.94%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8077 80.77%
P-glycoprotein inhibitior - 0.9771 97.71%
P-glycoprotein substrate - 0.8907 89.07%
CYP3A4 substrate - 0.5748 57.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7571 75.71%
CYP3A4 inhibition - 0.8293 82.93%
CYP2C9 inhibition - 0.6282 62.82%
CYP2C19 inhibition + 0.5085 50.85%
CYP2D6 inhibition - 0.9343 93.43%
CYP1A2 inhibition + 0.6767 67.67%
CYP2C8 inhibition - 0.6159 61.59%
CYP inhibitory promiscuity - 0.6465 64.65%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5194 51.94%
Eye corrosion - 0.9820 98.20%
Eye irritation + 0.7559 75.59%
Skin irritation - 0.6667 66.67%
Skin corrosion - 0.9107 91.07%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5135 51.35%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.5590 55.90%
skin sensitisation - 0.8804 88.04%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.6842 68.42%
Acute Oral Toxicity (c) I 0.4092 40.92%
Estrogen receptor binding + 0.7924 79.24%
Androgen receptor binding - 0.4919 49.19%
Thyroid receptor binding - 0.6352 63.52%
Glucocorticoid receptor binding + 0.7828 78.28%
Aromatase binding + 0.5620 56.20%
PPAR gamma + 0.7436 74.36%
Honey bee toxicity - 0.9503 95.03%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9225 92.25%

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 99.24% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.19% 99.17%
CHEMBL2581 P07339 Cathepsin D 93.06% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.72% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.88% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.50% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 88.11% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.17% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.10% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.63% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.30% 99.15%
CHEMBL2216739 Q92523 Carnitine O-palmitoyltransferase 1, muscle isoform 81.79% 88.33%

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.
Dorstenia psilurus

Cross-Links

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PubChem 15391031
LOTUS LTS0247065
wikiData Q105181558