(Z)-Ferulic acid 4-O-beta-D-glucoside

Details

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Internal ID 6a2b1183-d56d-4f53-9aa7-53e76f8a6397
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name (Z)-3-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid
SMILES (Canonical) COC1=C(C=CC(=C1)C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)/C=C\C(=O)O)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O
InChI InChI=1S/C16H20O9/c1-23-10-6-8(3-5-12(18)19)2-4-9(10)24-16-15(22)14(21)13(20)11(7-17)25-16/h2-6,11,13-17,20-22H,7H2,1H3,(H,18,19)/b5-3-/t11-,13-,14+,15-,16-/m1/s1
InChI Key IEMIRSXOYFWPFD-QEQKPWIDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O9
Molecular Weight 356.32 g/mol
Exact Mass 356.11073221 g/mol
Topological Polar Surface Area (TPSA) 146.00 Ų
XlogP -1.10
Atomic LogP (AlogP) -1.03
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

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CIS-FERULIC ACID 4-O-BETA-D-GLUCOPYRANOSIDE
4-(beta-D-Glucopyranosyloxy)-3-methoxy-cis-cinnamic acid
94942-20-8

2D Structure

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2D Structure of (Z)-Ferulic acid 4-O-beta-D-glucoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5999 59.99%
Caco-2 - 0.8423 84.23%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6113 61.13%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.8946 89.46%
OATP1B3 inhibitior + 0.9745 97.45%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6087 60.87%
P-glycoprotein inhibitior - 0.8945 89.45%
P-glycoprotein substrate - 0.9024 90.24%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8004 80.04%
CYP2D6 substrate - 0.8631 86.31%
CYP3A4 inhibition - 0.8029 80.29%
CYP2C9 inhibition - 0.8622 86.22%
CYP2C19 inhibition - 0.8645 86.45%
CYP2D6 inhibition - 0.9104 91.04%
CYP1A2 inhibition - 0.8780 87.80%
CYP2C8 inhibition + 0.5987 59.87%
CYP inhibitory promiscuity - 0.5991 59.91%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7362 73.62%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.9425 94.25%
Skin irritation - 0.8038 80.38%
Skin corrosion - 0.9548 95.48%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6058 60.58%
Micronuclear + 0.5233 52.33%
Hepatotoxicity - 0.8500 85.00%
skin sensitisation - 0.8220 82.20%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.8680 86.80%
Acute Oral Toxicity (c) III 0.7589 75.89%
Estrogen receptor binding - 0.6488 64.88%
Androgen receptor binding - 0.5343 53.43%
Thyroid receptor binding + 0.5156 51.56%
Glucocorticoid receptor binding - 0.5234 52.34%
Aromatase binding - 0.6232 62.32%
PPAR gamma + 0.5844 58.44%
Honey bee toxicity - 0.8733 87.33%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6755 67.55%
Fish aquatic toxicity + 0.6926 69.26%

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
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 97.74% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.75% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.22% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.23% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.07% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.51% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.09% 95.56%
CHEMBL3194 P02766 Transthyretin 84.37% 90.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.35% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 83.30% 94.73%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.44% 89.62%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.25% 86.92%
CHEMBL4208 P20618 Proteasome component C5 80.47% 90.00%

Cross-Links

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PubChem 9820054
NPASS NPC74404
LOTUS LTS0155361
wikiData Q105111855