5-Hydroxymethylfuran-3-carboxylic acid

Details

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Internal ID aad3ea97-aef9-4b57-9d81-9a61856a849e
Taxonomy Organoheterocyclic compounds > Furans > Furoic acid and derivatives > Furoic acids
IUPAC Name 5-(hydroxymethyl)furan-3-carboxylic acid
SMILES (Canonical) C1=C(OC=C1C(=O)O)CO
SMILES (Isomeric) C1=C(OC=C1C(=O)O)CO
InChI InChI=1S/C6H6O4/c7-2-5-1-4(3-10-5)6(8)9/h1,3,7H,2H2,(H,8,9)
InChI Key ZEACFIAQNKKVPN-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C6H6O4
Molecular Weight 142.11 g/mol
Exact Mass 142.02660867 g/mol
Topological Polar Surface Area (TPSA) 70.70 Ų
XlogP -0.30
Atomic LogP (AlogP) 0.47
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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246178-75-6
5-hydroxymethylfuran-3-carboxylic acid
DTXSID80572634
RefChem:102914
DTXCID00523406
5-(Hydroxymethyl)furan-3-carboxylate
833-303-9
3-Furancarboxylic acid, 5-(hydroxymethyl)-
SCHEMBL3124525
CHEBI:218793
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5-Hydroxymethylfuran-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 + 0.9098 90.98%
Caco-2 - 0.6615 66.15%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7478 74.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9061 90.61%
OATP1B3 inhibitior + 0.9367 93.67%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9669 96.69%
P-glycoprotein inhibitior - 0.9772 97.72%
P-glycoprotein substrate - 0.9858 98.58%
CYP3A4 substrate - 0.7792 77.92%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8888 88.88%
CYP3A4 inhibition - 0.9668 96.68%
CYP2C9 inhibition - 0.9318 93.18%
CYP2C19 inhibition - 0.9193 91.93%
CYP2D6 inhibition - 0.9643 96.43%
CYP1A2 inhibition - 0.6853 68.53%
CYP2C8 inhibition - 0.8814 88.14%
CYP inhibitory promiscuity - 0.8715 87.15%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5160 51.60%
Eye corrosion - 0.8003 80.03%
Eye irritation + 0.9917 99.17%
Skin irritation - 0.5519 55.19%
Skin corrosion - 0.7342 73.42%
Ames mutagenesis + 0.5777 57.77%
Human Ether-a-go-go-Related Gene inhibition - 0.8998 89.98%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.5056 50.56%
skin sensitisation - 0.8388 83.88%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.6708 67.08%
Acute Oral Toxicity (c) III 0.6342 63.42%
Estrogen receptor binding - 0.8814 88.14%
Androgen receptor binding - 0.7025 70.25%
Thyroid receptor binding - 0.8497 84.97%
Glucocorticoid receptor binding - 0.8043 80.43%
Aromatase binding - 0.7234 72.34%
PPAR gamma - 0.7054 70.54%
Honey bee toxicity - 0.9732 97.32%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity - 0.8102 81.02%

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
CHEMBL1293294 P51151 Ras-related protein Rab-9A 90.03% 87.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.20% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.47% 99.17%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 87.16% 81.11%
CHEMBL1811 P34995 Prostanoid EP1 receptor 85.03% 95.71%
CHEMBL3401 O75469 Pregnane X receptor 81.48% 94.73%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 80.87% 89.67%

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 15422126
LOTUS LTS0117276
wikiData Q77567036