5-Hydroxy-methylfuran-2-carboxylic

Details

Top
Internal ID daa51b64-280a-4223-8adb-29b70e88987b
Taxonomy Organoheterocyclic compounds > Furans > Furoic acid and derivatives > Furoic acids
IUPAC Name 5-hydroxy-3-methylfuran-2-carboxylic acid
SMILES (Canonical) CC1=C(OC(=C1)O)C(=O)O
SMILES (Isomeric) CC1=C(OC(=C1)O)C(=O)O
InChI InChI=1S/C6H6O4/c1-3-2-4(7)10-5(3)6(8)9/h2,7H,1H3,(H,8,9)
InChI Key YLDRQCRVPFKVGN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H6O4
Molecular Weight 142.11 g/mol
Exact Mass 142.02660867 g/mol
Topological Polar Surface Area (TPSA) 70.70 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.99
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
5-hydroxy-methylfuran-2-carboxylic

2D Structure

Top
2D Structure of 5-Hydroxy-methylfuran-2-carboxylic

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9669 96.69%
Caco-2 + 0.6464 64.64%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8319 83.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9495 94.95%
OATP1B3 inhibitior + 0.9331 93.31%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9569 95.69%
P-glycoprotein inhibitior - 0.9680 96.80%
P-glycoprotein substrate - 0.9881 98.81%
CYP3A4 substrate - 0.7631 76.31%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.9144 91.44%
CYP3A4 inhibition - 0.9349 93.49%
CYP2C9 inhibition - 0.8097 80.97%
CYP2C19 inhibition - 0.7842 78.42%
CYP2D6 inhibition - 0.9646 96.46%
CYP1A2 inhibition + 0.5327 53.27%
CYP2C8 inhibition - 0.9403 94.03%
CYP inhibitory promiscuity - 0.7364 73.64%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8818 88.18%
Carcinogenicity (trinary) Non-required 0.5002 50.02%
Eye corrosion - 0.6476 64.76%
Eye irritation + 0.9826 98.26%
Skin irritation + 0.6076 60.76%
Skin corrosion - 0.6243 62.43%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7490 74.90%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.6880 68.80%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.6094 60.94%
Acute Oral Toxicity (c) III 0.5275 52.75%
Estrogen receptor binding - 0.9043 90.43%
Androgen receptor binding - 0.8409 84.09%
Thyroid receptor binding - 0.8393 83.93%
Glucocorticoid receptor binding - 0.8700 87.00%
Aromatase binding - 0.8345 83.45%
PPAR gamma - 0.6570 65.70%
Honey bee toxicity - 0.9870 98.70%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6476 64.76%
Fish aquatic toxicity + 0.8318 83.18%

Targets

Top

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 90.39% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 89.98% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.46% 95.56%
CHEMBL1811 P34995 Prostanoid EP1 receptor 84.86% 95.71%
CHEMBL2581 P07339 Cathepsin D 82.97% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.95% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.86% 89.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.46% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.46% 99.17%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.11% 81.11%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.57% 94.42%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 21475716
LOTUS LTS0143935
wikiData Q105350088