Methyl furan-3-carboxylate

Details

Top
Internal ID cc88bd79-e869-45c7-b17a-436734ed0e58
Taxonomy Organoheterocyclic compounds > Furans > Furoic acid and derivatives > Furoic acid esters
IUPAC Name methyl furan-3-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H6O3/c1-8-6(7)5-2-3-9-4-5/h2-4H,1H3
InChI Key ZKHQSQYLKSSYIP-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H6O3
Molecular Weight 126.11 g/mol
Exact Mass 126.031694049 g/mol
Topological Polar Surface Area (TPSA) 39.40 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.07
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
Methyl 3-furoate
Methyl 3-furancarboxylate
3-(Methoxycarbonyl)furan
NSC-305748
UNII-V05P3H54N5
V05P3H54N5
NSC 305748
RefChem:157871
672-679-7
ZKHQSQYLKSSYIP-UHFFFAOYSA-N
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Methyl furan-3-carboxylate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.7950 79.50%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.6612 66.12%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8439 84.39%
OATP1B3 inhibitior + 0.9741 97.41%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9496 94.96%
P-glycoprotein inhibitior - 0.9829 98.29%
P-glycoprotein substrate - 0.9796 97.96%
CYP3A4 substrate - 0.6345 63.45%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8580 85.80%
CYP3A4 inhibition - 0.9822 98.22%
CYP2C9 inhibition - 0.9017 90.17%
CYP2C19 inhibition - 0.7215 72.15%
CYP2D6 inhibition - 0.9463 94.63%
CYP1A2 inhibition + 0.6743 67.43%
CYP2C8 inhibition - 0.8134 81.34%
CYP inhibitory promiscuity - 0.7578 75.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.4576 45.76%
Eye corrosion + 0.9468 94.68%
Eye irritation + 0.9946 99.46%
Skin irritation + 0.5826 58.26%
Skin corrosion - 0.6797 67.97%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7315 73.15%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.5527 55.27%
skin sensitisation - 0.6217 62.17%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.4676 46.76%
Acute Oral Toxicity (c) III 0.4976 49.76%
Estrogen receptor binding - 0.9593 95.93%
Androgen receptor binding - 0.9406 94.06%
Thyroid receptor binding - 0.8999 89.99%
Glucocorticoid receptor binding - 0.9487 94.87%
Aromatase binding - 0.8391 83.91%
PPAR gamma - 0.9357 93.57%
Honey bee toxicity - 0.9760 97.60%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity - 0.3818 38.18%

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
CHEMBL1293294 P51151 Ras-related protein Rab-9A 86.49% 87.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.22% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 85.27% 94.73%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 84.45% 81.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.61% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.37% 91.11%
CHEMBL4208 P20618 Proteasome component C5 82.34% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.84% 86.33%

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.
Ephedra sinica

Cross-Links

Top
PubChem 14918
NPASS NPC137742