6-Methoxybenzofuran-5-carboxamide

Details

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Internal ID 3f356b3c-2eea-4445-9e78-cd274f7b1efd
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 6-methoxy-1-benzofuran-5-carboxamide
SMILES (Canonical) COC1=C(C=C2C=COC2=C1)C(=O)N
SMILES (Isomeric) COC1=C(C=C2C=COC2=C1)C(=O)N
InChI InChI=1S/C10H9NO3/c1-13-9-5-8-6(2-3-14-8)4-7(9)10(11)12/h2-5H,1H3,(H2,11,12)
InChI Key VBQCMRHLMURRPU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H9NO3
Molecular Weight 191.18 g/mol
Exact Mass 191.058243149 g/mol
Topological Polar Surface Area (TPSA) 65.50 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.54
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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6-methoxybenzofuran-5-carboxamide

2D Structure

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2D Structure of 6-Methoxybenzofuran-5-carboxamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8047 80.47%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5091 50.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9716 97.16%
OATP1B3 inhibitior + 0.9793 97.93%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7283 72.83%
P-glycoprotein inhibitior - 0.9360 93.60%
P-glycoprotein substrate - 0.8442 84.42%
CYP3A4 substrate - 0.6498 64.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8366 83.66%
CYP3A4 inhibition - 0.9124 91.24%
CYP2C9 inhibition - 0.8940 89.40%
CYP2C19 inhibition - 0.8019 80.19%
CYP2D6 inhibition - 0.9170 91.70%
CYP1A2 inhibition + 0.8942 89.42%
CYP2C8 inhibition - 0.7294 72.94%
CYP inhibitory promiscuity - 0.7176 71.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8540 85.40%
Carcinogenicity (trinary) Non-required 0.4404 44.04%
Eye corrosion - 0.9783 97.83%
Eye irritation - 0.4835 48.35%
Skin irritation - 0.8407 84.07%
Skin corrosion - 0.9748 97.48%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5371 53.71%
Micronuclear + 0.7459 74.59%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.9158 91.58%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.5662 56.62%
Acute Oral Toxicity (c) III 0.5752 57.52%
Estrogen receptor binding - 0.4827 48.27%
Androgen receptor binding - 0.5882 58.82%
Thyroid receptor binding - 0.7976 79.76%
Glucocorticoid receptor binding + 0.5593 55.93%
Aromatase binding + 0.7021 70.21%
PPAR gamma - 0.5165 51.65%
Honey bee toxicity - 0.9605 96.05%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6749 67.49%
Fish aquatic toxicity - 0.4854 48.54%

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 94.97% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.79% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.30% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.53% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.12% 94.00%
CHEMBL1255126 O15151 Protein Mdm4 84.30% 90.20%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.74% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.31% 95.56%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.22% 94.42%

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.
Tephrosia purpurea

Cross-Links

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PubChem 122195903
LOTUS LTS0086762
wikiData Q105283423