6-O-Acetylglucose

Details

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Internal ID 335775c8-9ce6-4da7-9d8c-bb928a943f9b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides
IUPAC Name (3,4,5,6-tetrahydroxyoxan-2-yl)methyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H14O7/c1-3(9)14-2-4-5(10)6(11)7(12)8(13)15-4/h4-8,10-13H,2H2,1H3
InChI Key ILLOJQCWUBEHBA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14O7
Molecular Weight 222.19 g/mol
Exact Mass 222.07395278 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP -2.60
Atomic LogP (AlogP) -2.65
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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RefChem:935947
GlyTouCan:G99613WT
G99613WT
(3,4,5,6-tetrahydroxyoxan-2-yl)methyl acetate
SCHEMBL12427214
CHEBI:189030
(3,4,5,6-tetrahydroxytetrahydropyran-2-yl)methyl acetate

2D Structure

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2D Structure of 6-O-Acetylglucose

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 - 0.9268 92.68%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8360 83.60%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.8579 85.79%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8834 88.34%
P-glycoprotein inhibitior - 0.9662 96.62%
P-glycoprotein substrate - 0.9895 98.95%
CYP3A4 substrate - 0.5662 56.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8819 88.19%
CYP3A4 inhibition - 0.9663 96.63%
CYP2C9 inhibition - 0.9595 95.95%
CYP2C19 inhibition - 0.9643 96.43%
CYP2D6 inhibition - 0.9499 94.99%
CYP1A2 inhibition - 0.9456 94.56%
CYP2C8 inhibition - 0.9667 96.67%
CYP inhibitory promiscuity - 0.9470 94.70%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7524 75.24%
Eye corrosion - 0.9816 98.16%
Eye irritation - 0.9655 96.55%
Skin irritation - 0.7950 79.50%
Skin corrosion - 0.9473 94.73%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7289 72.89%
Micronuclear - 0.6867 68.67%
Hepatotoxicity - 0.7569 75.69%
skin sensitisation - 0.9258 92.58%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.5290 52.90%
Acute Oral Toxicity (c) III 0.5324 53.24%
Estrogen receptor binding - 0.8307 83.07%
Androgen receptor binding - 0.8522 85.22%
Thyroid receptor binding - 0.6108 61.08%
Glucocorticoid receptor binding - 0.7649 76.49%
Aromatase binding - 0.8106 81.06%
PPAR gamma - 0.7806 78.06%
Honey bee toxicity - 0.8502 85.02%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7655 76.55%
Fish aquatic toxicity - 0.6351 63.51%

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 96.35% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 94.74% 83.82%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.81% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 86.98% 94.73%
CHEMBL226 P30542 Adenosine A1 receptor 85.60% 95.93%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.54% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.92% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.45% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.55% 99.17%
CHEMBL2581 P07339 Cathepsin D 82.00% 98.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.76% 94.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.59% 85.14%

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.
Ligularia atroviolacea

Cross-Links

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PubChem 536270
LOTUS LTS0150141
wikiData Q77492447