3-(furan-2-ylmethyl)-1H-pyrrole-2-carboxylic acid

Details

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Internal ID cb8e223d-2798-4f9a-b04a-8a2dd23cac19
Taxonomy Organoheterocyclic compounds > Pyrroles > Pyrrole carboxylic acids and derivatives > Pyrrole carboxylic acids > Pyrrole 2-carboxylic acids
IUPAC Name 3-(furan-2-ylmethyl)-1H-pyrrole-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H9NO3/c12-10(13)9-7(3-4-11-9)6-8-2-1-5-14-8/h1-5,11H,6H2,(H,12,13)
InChI Key MRTZXPRKQXMJMT-UHFFFAOYSA-N
Popularity 3 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) 66.20 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.90
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(furan-2-ylmethyl)-1H-pyrrole-2-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9421 94.21%
Caco-2 + 0.4925 49.25%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.7316 73.16%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9277 92.77%
OATP1B3 inhibitior + 0.9457 94.57%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9089 90.89%
P-glycoprotein inhibitior - 0.9793 97.93%
P-glycoprotein substrate - 0.9397 93.97%
CYP3A4 substrate - 0.6548 65.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8837 88.37%
CYP3A4 inhibition - 0.9684 96.84%
CYP2C9 inhibition - 0.8881 88.81%
CYP2C19 inhibition - 0.8607 86.07%
CYP2D6 inhibition - 0.9431 94.31%
CYP1A2 inhibition - 0.8529 85.29%
CYP2C8 inhibition - 0.8131 81.31%
CYP inhibitory promiscuity - 0.9072 90.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6550 65.50%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.7241 72.41%
Skin irritation - 0.7395 73.95%
Skin corrosion - 0.9013 90.13%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6094 60.94%
Micronuclear + 0.7000 70.00%
Hepatotoxicity - 0.6069 60.69%
skin sensitisation - 0.8681 86.81%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.5670 56.70%
Acute Oral Toxicity (c) III 0.5822 58.22%
Estrogen receptor binding - 0.7209 72.09%
Androgen receptor binding - 0.8145 81.45%
Thyroid receptor binding - 0.7797 77.97%
Glucocorticoid receptor binding - 0.4880 48.80%
Aromatase binding + 0.5680 56.80%
PPAR gamma + 0.7574 75.74%
Honey bee toxicity - 0.9468 94.68%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity - 0.6593 65.93%

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 96.66% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.34% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.56% 95.56%
CHEMBL2581 P07339 Cathepsin D 85.63% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.13% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 80.08% 94.73%

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 90865811
LOTUS LTS0023636
wikiData Q105170931