Methyl 5-formyl-1-benzofuran-6-carboxylate

Details

Top
Internal ID 900e9e99-e9d1-42aa-8353-9d8bd96071c4
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name methyl 5-formyl-1-benzofuran-6-carboxylate
SMILES (Canonical) COC(=O)C1=C(C=C2C=COC2=C1)C=O
SMILES (Isomeric) COC(=O)C1=C(C=C2C=COC2=C1)C=O
InChI InChI=1S/C11H8O4/c1-14-11(13)9-5-10-7(2-3-15-10)4-8(9)6-12/h2-6H,1H3
InChI Key NYZYGLCVCLCBFA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C11H8O4
Molecular Weight 204.18 g/mol
Exact Mass 204.04225873 g/mol
Topological Polar Surface Area (TPSA) 56.50 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.03
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Methyl 5-formyl-1-benzofuran-6-carboxylate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9900 99.00%
Caco-2 + 0.7998 79.98%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6659 66.59%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8461 84.61%
OATP1B3 inhibitior + 0.9839 98.39%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9245 92.45%
P-glycoprotein inhibitior - 0.9263 92.63%
P-glycoprotein substrate - 0.9205 92.05%
CYP3A4 substrate - 0.5852 58.52%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8590 85.90%
CYP3A4 inhibition - 0.9267 92.67%
CYP2C9 inhibition - 0.6753 67.53%
CYP2C19 inhibition - 0.6610 66.10%
CYP2D6 inhibition - 0.9654 96.54%
CYP1A2 inhibition + 0.8950 89.50%
CYP2C8 inhibition - 0.6503 65.03%
CYP inhibitory promiscuity - 0.5899 58.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8053 80.53%
Carcinogenicity (trinary) Non-required 0.5167 51.67%
Eye corrosion - 0.9140 91.40%
Eye irritation + 0.7509 75.09%
Skin irritation - 0.7403 74.03%
Skin corrosion - 0.9746 97.46%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4811 48.11%
Micronuclear + 0.5459 54.59%
Hepatotoxicity + 0.5099 50.99%
skin sensitisation - 0.7349 73.49%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.6377 63.77%
Acute Oral Toxicity (c) III 0.5450 54.50%
Estrogen receptor binding - 0.5280 52.80%
Androgen receptor binding + 0.5894 58.94%
Thyroid receptor binding - 0.6909 69.09%
Glucocorticoid receptor binding - 0.6216 62.16%
Aromatase binding + 0.6971 69.71%
PPAR gamma - 0.7935 79.35%
Honey bee toxicity - 0.9451 94.51%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9639 96.39%

Targets

Top

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 93.62% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.61% 86.33%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 88.93% 87.67%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.45% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 87.15% 94.73%
CHEMBL2581 P07339 Cathepsin D 86.84% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.02% 94.45%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 85.92% 98.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.77% 96.09%
CHEMBL4208 P20618 Proteasome component C5 85.11% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.87% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.49% 96.00%

Plants that contains it

Top
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.
Pulicaria wightiana

Cross-Links

Top
PubChem 102026829
LOTUS LTS0011864
wikiData Q105187797