(E)-3-(3-hydroxy-4-O-a-fucofuranosylphenyl)-2-methylacrylic acid

Details

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Internal ID 64e352e5-c330-4164-bb98-9626a590bd1b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name (E)-3-[4-[(2S,3S,4S,5R)-3,4-dihydroxy-5-[(1S)-1-hydroxyethyl]oxolan-2-yl]oxy-3-hydroxyphenyl]-2-methylprop-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H20O8/c1-7(15(21)22)5-9-3-4-11(10(18)6-9)23-16-13(20)12(19)14(24-16)8(2)17/h3-6,8,12-14,16-20H,1-2H3,(H,21,22)/b7-5+/t8-,12-,13-,14+,16+/m0/s1
InChI Key KODWUJKPORHWMA-HDGKHBOVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O8
Molecular Weight 340.32 g/mol
Exact Mass 340.11581759 g/mol
Topological Polar Surface Area (TPSA) 137.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.09
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E)-3-(3-hydroxy-4-O-a-fucofuranosylphenyl)-2-methylacrylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9270 92.70%
Caco-2 - 0.7918 79.18%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7203 72.03%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.9413 94.13%
OATP1B3 inhibitior + 0.9518 95.18%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8174 81.74%
P-glycoprotein inhibitior - 0.9240 92.40%
P-glycoprotein substrate - 0.8557 85.57%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8838 88.38%
CYP3A4 inhibition - 0.6853 68.53%
CYP2C9 inhibition - 0.5802 58.02%
CYP2C19 inhibition + 0.6602 66.02%
CYP2D6 inhibition - 0.9065 90.65%
CYP1A2 inhibition + 0.6743 67.43%
CYP2C8 inhibition - 0.7208 72.08%
CYP inhibitory promiscuity + 0.8374 83.74%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8951 89.51%
Carcinogenicity (trinary) Non-required 0.5109 51.09%
Eye corrosion - 0.9520 95.20%
Eye irritation - 0.7895 78.95%
Skin irritation - 0.6410 64.10%
Skin corrosion - 0.9299 92.99%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6810 68.10%
Micronuclear + 0.8300 83.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.5420 54.20%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.7870 78.70%
Acute Oral Toxicity (c) III 0.4688 46.88%
Estrogen receptor binding - 0.4804 48.04%
Androgen receptor binding - 0.6789 67.89%
Thyroid receptor binding + 0.6479 64.79%
Glucocorticoid receptor binding - 0.5753 57.53%
Aromatase binding - 0.5446 54.46%
PPAR gamma - 0.5171 51.71%
Honey bee toxicity - 0.8932 89.32%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9783 97.83%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.16% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.59% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.71% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.74% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.31% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 91.92% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.25% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.35% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.20% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.72% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.49% 99.15%
CHEMBL3194 P02766 Transthyretin 86.29% 90.71%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 84.58% 83.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.51% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.43% 90.71%
CHEMBL4208 P20618 Proteasome component C5 83.15% 90.00%

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 139584872
LOTUS LTS0265663
wikiData Q77377263