Furan-3-ylmethyl 1H-pyrrole-2-carboxylate

Details

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Internal ID 20828267-79ef-4058-b6d1-06c05d0738da
Taxonomy Organoheterocyclic compounds > Pyrroles > Pyrrole carboxylic acids and derivatives
IUPAC Name furan-3-ylmethyl 1H-pyrrole-2-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H9NO3/c12-10(9-2-1-4-11-9)14-7-8-3-5-13-6-8/h1-6,11H,7H2
InChI Key CSYQMTPUTVJNPT-UHFFFAOYSA-N
Popularity 2 references 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) 55.20 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.96
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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3-Furfuryl 2-pyrrolecarboxylate
Furan-3-ylmethyl 1H-pyrrole-2-carboxylate
3-Furfuryl pyrrole-2-carboxylate
3-?Furfuryl 2-?pyrrolecarboxylate
3-furylmethyl 1H-pyrrole-2-carboxylate
3-urfuryl 2-yrrolecarboxylate
3-Furfuryl2-pyrrolecarboxylate
orb1708092
SCHEMBL30560992
DTXSID60152579
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Furan-3-ylmethyl 1H-pyrrole-2-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9897 98.97%
Caco-2 + 0.7153 71.53%
Blood Brain Barrier + 0.8778 87.78%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6595 65.95%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8504 85.04%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7294 72.94%
P-glycoprotein inhibitior - 0.9854 98.54%
P-glycoprotein substrate - 0.9278 92.78%
CYP3A4 substrate - 0.5474 54.74%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8422 84.22%
CYP3A4 inhibition - 0.9203 92.03%
CYP2C9 inhibition - 0.6472 64.72%
CYP2C19 inhibition - 0.6312 63.12%
CYP2D6 inhibition - 0.8249 82.49%
CYP1A2 inhibition + 0.6313 63.13%
CYP2C8 inhibition - 0.5943 59.43%
CYP inhibitory promiscuity + 0.5274 52.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5932 59.32%
Eye corrosion - 0.9284 92.84%
Eye irritation + 0.8077 80.77%
Skin irritation - 0.5916 59.16%
Skin corrosion - 0.8264 82.64%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4788 47.88%
Micronuclear + 0.6400 64.00%
Hepatotoxicity - 0.5914 59.14%
skin sensitisation - 0.8899 88.99%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.7781 77.81%
Acute Oral Toxicity (c) III 0.6279 62.79%
Estrogen receptor binding - 0.6971 69.71%
Androgen receptor binding - 0.7950 79.50%
Thyroid receptor binding - 0.8323 83.23%
Glucocorticoid receptor binding - 0.8750 87.50%
Aromatase binding + 0.7334 73.34%
PPAR gamma - 0.7458 74.58%
Honey bee toxicity - 0.8812 88.12%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6505 65.05%
Fish aquatic toxicity - 0.5410 54.10%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.73% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.88% 94.45%
CHEMBL2581 P07339 Cathepsin D 92.33% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.83% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 89.75% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.47% 99.17%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 83.75% 89.67%
CHEMBL3401 O75469 Pregnane X receptor 83.20% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.99% 94.00%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.50% 97.28%
CHEMBL3891 P07384 Calpain 1 80.01% 93.04%

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.
Pseudostellaria heterophylla

Cross-Links

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PubChem 189695
NPASS NPC202873
LOTUS LTS0007907
wikiData Q72505054