2-Phenylethyl 6-O-beta-D-glucopyranosyl-beta-D-glucopyranoside

Details

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Internal ID 66c0c603-fe75-4e00-915f-8c99e8ea0b53
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-(2-phenylethoxy)oxan-2-yl]methoxy]oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H30O11/c21-8-11-13(22)15(24)18(27)20(30-11)29-9-12-14(23)16(25)17(26)19(31-12)28-7-6-10-4-2-1-3-5-10/h1-5,11-27H,6-9H2/t11-,12-,13-,14-,15+,16+,17-,18-,19-,20-/m1/s1
InChI Key UKPSYYFYNMESBQ-XSVWGIRKSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O11
Molecular Weight 446.40 g/mol
Exact Mass 446.17881177 g/mol
Topological Polar Surface Area (TPSA) 179.00 Ų
XlogP -2.20
Atomic LogP (AlogP) -3.13
H-Bond Acceptor 11
H-Bond Donor 7
Rotatable Bonds 8

Synonyms

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2-Phenylethyl 6-O-beta-D-glucopyranosyl-beta-D-glucopyranoside
TN11781

2D Structure

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2D Structure of 2-Phenylethyl 6-O-beta-D-glucopyranosyl-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 - 0.9506 95.06%
Caco-2 - 0.8523 85.23%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.7792 77.92%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8953 89.53%
OATP1B3 inhibitior + 0.9508 95.08%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7998 79.98%
P-glycoprotein inhibitior - 0.8283 82.83%
P-glycoprotein substrate - 0.9426 94.26%
CYP3A4 substrate - 0.5329 53.29%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7873 78.73%
CYP3A4 inhibition - 0.9602 96.02%
CYP2C9 inhibition - 0.8109 81.09%
CYP2C19 inhibition - 0.8599 85.99%
CYP2D6 inhibition - 0.9281 92.81%
CYP1A2 inhibition - 0.9404 94.04%
CYP2C8 inhibition + 0.4531 45.31%
CYP inhibitory promiscuity - 0.8722 87.22%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6143 61.43%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9425 94.25%
Skin irritation - 0.8554 85.54%
Skin corrosion - 0.9702 97.02%
Ames mutagenesis - 0.6470 64.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7075 70.75%
Micronuclear - 0.8241 82.41%
Hepatotoxicity - 0.8893 88.93%
skin sensitisation - 0.9133 91.33%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.7162 71.62%
Acute Oral Toxicity (c) III 0.5037 50.37%
Estrogen receptor binding + 0.5347 53.47%
Androgen receptor binding - 0.6613 66.13%
Thyroid receptor binding + 0.5580 55.80%
Glucocorticoid receptor binding - 0.6366 63.66%
Aromatase binding + 0.7184 71.84%
PPAR gamma + 0.6987 69.87%
Honey bee toxicity - 0.8103 81.03%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity - 0.8173 81.73%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 98.29% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.49% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.94% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.00% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.19% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.69% 86.33%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 88.47% 94.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.94% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 82.03% 90.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.32% 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.
Helichrysum arenarium
Staphylea bumalda

Cross-Links

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PubChem 11539591
LOTUS LTS0068399
wikiData Q105274786