(3,4,5-Trihydroxy-6-methyloxan-2-yl) 2,4-dimethylfuran-3-carboxylate

Details

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Internal ID d1b599b9-28d5-4605-9093-c8b181fec6ee
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Hexoses
IUPAC Name (3,4,5-trihydroxy-6-methyloxan-2-yl) 2,4-dimethylfuran-3-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H18O7/c1-5-4-18-6(2)8(5)12(17)20-13-11(16)10(15)9(14)7(3)19-13/h4,7,9-11,13-16H,1-3H3
InChI Key YCEOZBKOASFXBF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18O7
Molecular Weight 286.28 g/mol
Exact Mass 286.10525291 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.12
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3,4,5-Trihydroxy-6-methyloxan-2-yl) 2,4-dimethylfuran-3-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4657 46.57%
Caco-2 - 0.5224 52.24%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7684 76.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9092 90.92%
OATP1B3 inhibitior + 0.9066 90.66%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9187 91.87%
P-glycoprotein inhibitior - 0.8535 85.35%
P-glycoprotein substrate - 0.9413 94.13%
CYP3A4 substrate + 0.5099 50.99%
CYP2C9 substrate - 0.8080 80.80%
CYP2D6 substrate - 0.8683 86.83%
CYP3A4 inhibition - 0.8085 80.85%
CYP2C9 inhibition - 0.9459 94.59%
CYP2C19 inhibition - 0.8163 81.63%
CYP2D6 inhibition - 0.9159 91.59%
CYP1A2 inhibition - 0.7465 74.65%
CYP2C8 inhibition - 0.7431 74.31%
CYP inhibitory promiscuity - 0.6988 69.88%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9111 91.11%
Carcinogenicity (trinary) Non-required 0.5862 58.62%
Eye corrosion - 0.9641 96.41%
Eye irritation - 0.8736 87.36%
Skin irritation - 0.7509 75.09%
Skin corrosion - 0.9553 95.53%
Ames mutagenesis - 0.6654 66.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7341 73.41%
Micronuclear + 0.6800 68.00%
Hepatotoxicity - 0.5734 57.34%
skin sensitisation - 0.8233 82.33%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.8596 85.96%
Acute Oral Toxicity (c) III 0.5240 52.40%
Estrogen receptor binding - 0.5673 56.73%
Androgen receptor binding - 0.6565 65.65%
Thyroid receptor binding + 0.5414 54.14%
Glucocorticoid receptor binding - 0.6619 66.19%
Aromatase binding - 0.4915 49.15%
PPAR gamma - 0.6212 62.12%
Honey bee toxicity - 0.9230 92.30%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.7444 74.44%

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
CHEMBL3401 O75469 Pregnane X receptor 91.35% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.58% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.06% 89.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 87.86% 97.36%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.46% 86.33%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 86.08% 93.65%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.19% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.54% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.08% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.71% 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.
Baccharis coridifolia

Cross-Links

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PubChem 85159317
LOTUS LTS0110622
wikiData Q105023000