2-Butyl-4-(hydroxymethyl)furan-3-carboxylic acid

Details

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Internal ID 91b27a60-d937-467b-861c-3c6d2a9c4e47
Taxonomy Organoheterocyclic compounds > Furans > Furoic acid and derivatives > Furoic acids
IUPAC Name 2-butyl-4-(hydroxymethyl)furan-3-carboxylic acid
SMILES (Canonical) CCCCC1=C(C(=CO1)CO)C(=O)O
SMILES (Isomeric) CCCCC1=C(C(=CO1)CO)C(=O)O
InChI InChI=1S/C10H14O4/c1-2-3-4-8-9(10(12)13)7(5-11)6-14-8/h6,11H,2-5H2,1H3,(H,12,13)
InChI Key ZSSUULHTXZZTGE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O4
Molecular Weight 198.22 g/mol
Exact Mass 198.08920892 g/mol
Topological Polar Surface Area (TPSA) 70.70 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.81
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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CHEBI:220501
2-butyl-4-(hydroxymethyl)uran-3-carboxylic acid
2-butyl-4-(hydroxymethyl)-3-furancarboxylic acid

2D Structure

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2D Structure of 2-Butyl-4-(hydroxymethyl)furan-3-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 + 0.9532 95.32%
Caco-2 + 0.7545 75.45%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7590 75.90%
OATP2B1 inhibitior - 0.8485 84.85%
OATP1B1 inhibitior + 0.8905 89.05%
OATP1B3 inhibitior + 0.9535 95.35%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8713 87.13%
P-glycoprotein inhibitior - 0.9564 95.64%
P-glycoprotein substrate - 0.9143 91.43%
CYP3A4 substrate - 0.6456 64.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9005 90.05%
CYP3A4 inhibition - 0.8393 83.93%
CYP2C9 inhibition - 0.7851 78.51%
CYP2C19 inhibition - 0.7378 73.78%
CYP2D6 inhibition - 0.9379 93.79%
CYP1A2 inhibition - 0.6390 63.90%
CYP2C8 inhibition - 0.7999 79.99%
CYP inhibitory promiscuity - 0.7974 79.74%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.6606 66.06%
Eye corrosion - 0.9697 96.97%
Eye irritation + 0.8630 86.30%
Skin irritation - 0.6631 66.31%
Skin corrosion - 0.9140 91.40%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8032 80.32%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.5199 51.99%
skin sensitisation - 0.8559 85.59%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.5836 58.36%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.4841 48.41%
Acute Oral Toxicity (c) III 0.6556 65.56%
Estrogen receptor binding - 0.8929 89.29%
Androgen receptor binding - 0.5141 51.41%
Thyroid receptor binding - 0.7734 77.34%
Glucocorticoid receptor binding - 0.5323 53.23%
Aromatase binding - 0.8196 81.96%
PPAR gamma + 0.5652 56.52%
Honey bee toxicity - 0.9912 99.12%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.8988 89.88%

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
CHEMBL2581 P07339 Cathepsin D 95.20% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.47% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 89.76% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.03% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.90% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.65% 97.25%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.27% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.17% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.02% 86.33%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 81.20% 87.67%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 101483167
LOTUS LTS0019707
wikiData Q105382690