4-(Hydroxymethyl)-2-(3-methylbutyl)furan-3-carboxylic acid

Details

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Internal ID 56fc71b3-9fba-4885-a625-ba43139b3429
Taxonomy Organoheterocyclic compounds > Furans > Furoic acid and derivatives > Furoic acids
IUPAC Name 4-(hydroxymethyl)-2-(3-methylbutyl)furan-3-carboxylic acid
SMILES (Canonical) CC(C)CCC1=C(C(=CO1)CO)C(=O)O
SMILES (Isomeric) CC(C)CCC1=C(C(=CO1)CO)C(=O)O
InChI InChI=1S/C11H16O4/c1-7(2)3-4-9-10(11(13)14)8(5-12)6-15-9/h6-7,12H,3-5H2,1-2H3,(H,13,14)
InChI Key WCDZGGPOMQMYJJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16O4
Molecular Weight 212.24 g/mol
Exact Mass 212.10485899 g/mol
Topological Polar Surface Area (TPSA) 70.70 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(Hydroxymethyl)-2-(3-methylbutyl)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 + 0.9331 93.31%
Caco-2 + 0.6519 65.19%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.8307 83.07%
OATP2B1 inhibitior - 0.8502 85.02%
OATP1B1 inhibitior + 0.9272 92.72%
OATP1B3 inhibitior + 0.9499 94.99%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9240 92.40%
P-glycoprotein inhibitior - 0.9415 94.15%
P-glycoprotein substrate - 0.9268 92.68%
CYP3A4 substrate - 0.6308 63.08%
CYP2C9 substrate + 0.5906 59.06%
CYP2D6 substrate - 0.9001 90.01%
CYP3A4 inhibition - 0.8430 84.30%
CYP2C9 inhibition - 0.7843 78.43%
CYP2C19 inhibition - 0.8078 80.78%
CYP2D6 inhibition - 0.9248 92.48%
CYP1A2 inhibition - 0.6804 68.04%
CYP2C8 inhibition - 0.9669 96.69%
CYP inhibitory promiscuity - 0.8476 84.76%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.6956 69.56%
Eye corrosion - 0.9652 96.52%
Eye irritation + 0.7548 75.48%
Skin irritation - 0.7720 77.20%
Skin corrosion - 0.9391 93.91%
Ames mutagenesis - 0.5323 53.23%
Human Ether-a-go-go-Related Gene inhibition - 0.7805 78.05%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.7739 77.39%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.5006 50.06%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.5810 58.10%
Acute Oral Toxicity (c) III 0.5474 54.74%
Estrogen receptor binding - 0.9250 92.50%
Androgen receptor binding - 0.5499 54.99%
Thyroid receptor binding - 0.6140 61.40%
Glucocorticoid receptor binding - 0.6385 63.85%
Aromatase binding - 0.7552 75.52%
PPAR gamma + 0.6495 64.95%
Honey bee toxicity - 0.9713 97.13%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity + 0.9006 90.06%

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 94.25% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.24% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 91.80% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.89% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.75% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.39% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.95% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.19% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.25% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.10% 96.00%

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.
Fissistigma oldhamii
Incarvillea delavayi
Piper nigrum

Cross-Links

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PubChem 101483166
LOTUS LTS0012981
wikiData Q105251370