ethyl beta-D-glucopyranoside

Details

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Internal ID 90de8362-de58-45e8-ad3d-77b193a2bf6e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (2R,3R,4S,5S,6R)-2-ethoxy-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) CCOC1C(C(C(C(O1)CO)O)O)O
SMILES (Isomeric) CCO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
InChI InChI=1S/C8H16O6/c1-2-13-8-7(12)6(11)5(10)4(3-9)14-8/h4-12H,2-3H2,1H3/t4-,5-,6+,7-,8-/m1/s1
InChI Key WYUFTYLVLQZQNH-JAJWTYFOSA-N
Popularity 29 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16O6
Molecular Weight 208.21 g/mol
Exact Mass 208.09468823 g/mol
Topological Polar Surface Area (TPSA) 99.40 Ų
XlogP -1.80
Atomic LogP (AlogP) -2.18
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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Ethyl glucoside
3198-49-0
Ethyl D-glucoside
(2R,3R,4S,5S,6R)-2-ethoxy-6-(hydroxymethyl)oxane-3,4,5-triol
beta-D-Glucopyranoside, ethyl
AQ51A12T8K
EINECS 250-112-0
(2R,3R,4S,5S,6R)-2-ethoxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
C8H16O6
UNII-AQ51A12T8K
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of ethyl beta-D-glucopyranoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9164 91.64%
Caco-2 - 0.8962 89.62%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7289 72.89%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9297 92.97%
OATP1B3 inhibitior + 0.9633 96.33%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9638 96.38%
P-glycoprotein inhibitior - 0.9617 96.17%
P-glycoprotein substrate - 0.9867 98.67%
CYP3A4 substrate - 0.5928 59.28%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8487 84.87%
CYP3A4 inhibition - 0.9705 97.05%
CYP2C9 inhibition - 0.9274 92.74%
CYP2C19 inhibition - 0.8976 89.76%
CYP2D6 inhibition - 0.9551 95.51%
CYP1A2 inhibition - 0.9380 93.80%
CYP2C8 inhibition - 0.9563 95.63%
CYP inhibitory promiscuity - 0.9048 90.48%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6699 66.99%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.9793 97.93%
Skin irritation - 0.8765 87.65%
Skin corrosion - 0.9660 96.60%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6575 65.75%
Micronuclear - 0.8441 84.41%
Hepatotoxicity - 0.8324 83.24%
skin sensitisation - 0.9435 94.35%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.6769 67.69%
Acute Oral Toxicity (c) IV 0.5282 52.82%
Estrogen receptor binding - 0.9284 92.84%
Androgen receptor binding - 0.7521 75.21%
Thyroid receptor binding - 0.5340 53.40%
Glucocorticoid receptor binding - 0.7171 71.71%
Aromatase binding - 0.8289 82.89%
PPAR gamma - 0.7767 77.67%
Honey bee toxicity - 0.8494 84.94%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity - 0.8914 89.14%

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 93.82% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.45% 96.61%
CHEMBL3401 O75469 Pregnane X receptor 83.35% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.22% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.86% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 82.51% 95.93%
CHEMBL3589 P55263 Adenosine kinase 82.26% 98.05%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.22% 97.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.31% 99.17%

Cross-Links

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PubChem 121667
NPASS NPC244315