3-(6-Methoxy-1-benzofuran-5-yl)propanoic acid

Details

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Internal ID 7c962db7-749e-4e37-b50f-19f28963289d
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 3-(6-methoxy-1-benzofuran-5-yl)propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H12O4/c1-15-10-7-11-9(4-5-16-11)6-8(10)2-3-12(13)14/h4-7H,2-3H2,1H3,(H,13,14)
InChI Key YPJWDYIFUBTPCH-UHFFFAOYSA-N
Popularity 2 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) 2.46
H-Bond Acceptor 3
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 3-(6-Methoxy-1-benzofuran-5-yl)propanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.7774 77.74%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7601 76.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9183 91.83%
OATP1B3 inhibitior + 0.9410 94.10%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7229 72.29%
P-glycoprotein inhibitior - 0.9836 98.36%
P-glycoprotein substrate - 0.8449 84.49%
CYP3A4 substrate - 0.5803 58.03%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.7540 75.40%
CYP3A4 inhibition - 0.8582 85.82%
CYP2C9 inhibition - 0.8541 85.41%
CYP2C19 inhibition - 0.6923 69.23%
CYP2D6 inhibition - 0.9500 95.00%
CYP1A2 inhibition + 0.5746 57.46%
CYP2C8 inhibition - 0.5705 57.05%
CYP inhibitory promiscuity - 0.7826 78.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4923 49.23%
Eye corrosion - 0.9778 97.78%
Eye irritation + 0.6270 62.70%
Skin irritation - 0.7005 70.05%
Skin corrosion - 0.9393 93.93%
Ames mutagenesis - 0.7754 77.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5618 56.18%
Micronuclear - 0.5241 52.41%
Hepatotoxicity + 0.5181 51.81%
skin sensitisation - 0.8491 84.91%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7579 75.79%
Acute Oral Toxicity (c) III 0.4103 41.03%
Estrogen receptor binding + 0.5950 59.50%
Androgen receptor binding - 0.6822 68.22%
Thyroid receptor binding - 0.7708 77.08%
Glucocorticoid receptor binding + 0.6441 64.41%
Aromatase binding + 0.5795 57.95%
PPAR gamma + 0.8420 84.20%
Honey bee toxicity - 0.9417 94.17%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7155 71.55%
Fish aquatic toxicity + 0.7826 78.26%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 95.73% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.58% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.00% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.68% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 93.89% 90.20%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.86% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.55% 96.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.45% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.05% 95.56%

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.
Brosimum gaudichaudii

Cross-Links

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PubChem 163192342
LOTUS LTS0036652
wikiData Q105351715