1-O-(2,4-Dimethoxyphenyl)-beta-D-glucopyranose

Details

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Internal ID 17320610-45d1-4e7a-a7cc-2aa747224d84
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name (2S,3R,4S,5S,6R)-2-(2,4-dimethoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) COC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC
SMILES (Isomeric) COC1=CC(=C(C=C1)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)OC
InChI InChI=1S/C14H20O8/c1-19-7-3-4-8(9(5-7)20-2)21-14-13(18)12(17)11(16)10(6-15)22-14/h3-5,10-18H,6H2,1-2H3/t10-,11-,12+,13-,14-/m1/s1
InChI Key GVUJMEFPDAUWMK-RKQHYHRCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H20O8
Molecular Weight 316.30 g/mol
Exact Mass 316.11581759 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP -1.10
Atomic LogP (AlogP) -1.12
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-O-(2,4-Dimethoxyphenyl)-beta-D-glucopyranose

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7991 79.91%
Caco-2 - 0.7901 79.01%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6266 62.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9165 91.65%
OATP1B3 inhibitior + 0.9616 96.16%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7087 70.87%
P-glycoprotein inhibitior - 0.9224 92.24%
P-glycoprotein substrate - 0.9181 91.81%
CYP3A4 substrate - 0.5337 53.37%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7928 79.28%
CYP3A4 inhibition - 0.8453 84.53%
CYP2C9 inhibition - 0.8717 87.17%
CYP2C19 inhibition - 0.8517 85.17%
CYP2D6 inhibition - 0.9008 90.08%
CYP1A2 inhibition - 0.8683 86.83%
CYP2C8 inhibition - 0.6563 65.63%
CYP inhibitory promiscuity - 0.6831 68.31%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7283 72.83%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.9442 94.42%
Skin irritation - 0.8438 84.38%
Skin corrosion - 0.9589 95.89%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4167 41.67%
Micronuclear - 0.5541 55.41%
Hepatotoxicity - 0.8250 82.50%
skin sensitisation - 0.8629 86.29%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.7638 76.38%
Acute Oral Toxicity (c) III 0.7858 78.58%
Estrogen receptor binding - 0.7570 75.70%
Androgen receptor binding - 0.7694 76.94%
Thyroid receptor binding + 0.5439 54.39%
Glucocorticoid receptor binding - 0.5751 57.51%
Aromatase binding - 0.6313 63.13%
PPAR gamma - 0.5341 53.41%
Honey bee toxicity - 0.9172 91.72%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6649 66.49%
Fish aquatic toxicity - 0.5629 56.29%

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 97.49% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.53% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.88% 94.00%
CHEMBL4208 P20618 Proteasome component C5 90.15% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.07% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.39% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.10% 86.33%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.82% 86.92%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.41% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.03% 95.89%
CHEMBL3714130 P46095 G-protein coupled receptor 6 84.71% 97.36%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.72% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.31% 92.62%
CHEMBL3401 O75469 Pregnane X receptor 82.70% 94.73%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.80% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.07% 97.09%

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.
Asparagus officinalis
Astragalus dissectus
Ocotea minarum

Cross-Links

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PubChem 102392053
NPASS NPC112156