2,4,6-Trimethoxyphenol glucoside

Details

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Internal ID 09702f43-afc7-4744-b36e-f7bab2d40212
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 2-(hydroxymethyl)-6-(2,4,6-trimethoxyphenoxy)oxane-3,4,5-triol
SMILES (Canonical) COC1=CC(=C(C(=C1)OC)OC2C(C(C(C(O2)CO)O)O)O)OC
SMILES (Isomeric) COC1=CC(=C(C(=C1)OC)OC2C(C(C(C(O2)CO)O)O)O)OC
InChI InChI=1S/C15H22O9/c1-20-7-4-8(21-2)14(9(5-7)22-3)24-15-13(19)12(18)11(17)10(6-16)23-15/h4-5,10-13,15-19H,6H2,1-3H3
InChI Key YBNSHGZGFVJIGM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O9
Molecular Weight 346.33 g/mol
Exact Mass 346.12638228 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP -1.10
Atomic LogP (AlogP) -1.11
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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AKOS032948504

2D Structure

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2D Structure of 2,4,6-Trimethoxyphenol glucoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7906 79.06%
Caco-2 - 0.7831 78.31%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6152 61.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9195 91.95%
OATP1B3 inhibitior + 0.9471 94.71%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5763 57.63%
P-glycoprotein inhibitior - 0.8792 87.92%
P-glycoprotein substrate - 0.9514 95.14%
CYP3A4 substrate - 0.5520 55.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7928 79.28%
CYP3A4 inhibition - 0.8677 86.77%
CYP2C9 inhibition - 0.8715 87.15%
CYP2C19 inhibition - 0.8578 85.78%
CYP2D6 inhibition - 0.8960 89.60%
CYP1A2 inhibition - 0.8606 86.06%
CYP2C8 inhibition - 0.7452 74.52%
CYP inhibitory promiscuity - 0.7069 70.69%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7083 70.83%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.9401 94.01%
Skin irritation - 0.8570 85.70%
Skin corrosion - 0.9631 96.31%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4557 45.57%
Micronuclear - 0.5741 57.41%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation - 0.8813 88.13%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.7209 72.09%
Acute Oral Toxicity (c) III 0.7680 76.80%
Estrogen receptor binding - 0.7255 72.55%
Androgen receptor binding - 0.6847 68.47%
Thyroid receptor binding + 0.6635 66.35%
Glucocorticoid receptor binding - 0.4683 46.83%
Aromatase binding - 0.6207 62.07%
PPAR gamma + 0.6315 63.15%
Honey bee toxicity - 0.8973 89.73%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6849 68.49%
Fish aquatic toxicity - 0.5488 54.88%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.40% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.19% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.60% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.07% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.38% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.12% 96.00%
CHEMBL4208 P20618 Proteasome component C5 85.21% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.49% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 82.85% 94.73%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.49% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.31% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.77% 92.62%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.54% 86.92%

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.
Celastrus orbiculatus
Salacia chinensis
Strychnos spinosa
Syzygium levinei

Cross-Links

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PubChem 74037387
LOTUS LTS0152564
wikiData Q105345932