2-O-beta-D-glucopyranosyl-(1S)-phenylethylene glycol

Details

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Internal ID 9266ced9-da55-4f8d-ae4f-301af3a6a60e
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)-2-hydroxy-2-phenylethoxy]oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H20O7/c15-6-10-11(17)12(18)13(19)14(21-10)20-7-9(16)8-4-2-1-3-5-8/h1-5,9-19H,6-7H2/t9-,10+,11+,12-,13+,14+/m0/s1
InChI Key DDKQCNQJANTYLB-GMDXDWKASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H20O7
Molecular Weight 300.30 g/mol
Exact Mass 300.12090297 g/mol
Topological Polar Surface Area (TPSA) 120.00 Ų
XlogP -1.30
Atomic LogP (AlogP) -1.46
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-O-beta-D-glucopyranosyl-(1S)-phenylethylene glycol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9223 92.23%
Caco-2 - 0.8136 81.36%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6373 63.73%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.9395 93.95%
OATP1B3 inhibitior + 0.9441 94.41%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9777 97.77%
P-glycoprotein inhibitior - 0.9339 93.39%
P-glycoprotein substrate - 0.9700 97.00%
CYP3A4 substrate - 0.5958 59.58%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8134 81.34%
CYP3A4 inhibition - 0.9487 94.87%
CYP2C9 inhibition - 0.9469 94.69%
CYP2C19 inhibition - 0.9158 91.58%
CYP2D6 inhibition - 0.9289 92.89%
CYP1A2 inhibition - 0.9508 95.08%
CYP2C8 inhibition - 0.8788 87.88%
CYP inhibitory promiscuity - 0.8907 89.07%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6551 65.51%
Eye corrosion - 0.9948 99.48%
Eye irritation - 0.9456 94.56%
Skin irritation - 0.8585 85.85%
Skin corrosion - 0.9734 97.34%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6139 61.39%
Micronuclear - 0.7041 70.41%
Hepatotoxicity - 0.8000 80.00%
skin sensitisation - 0.9044 90.44%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.8419 84.19%
Acute Oral Toxicity (c) III 0.5672 56.72%
Estrogen receptor binding - 0.7900 79.00%
Androgen receptor binding - 0.7127 71.27%
Thyroid receptor binding - 0.5330 53.30%
Glucocorticoid receptor binding - 0.5655 56.55%
Aromatase binding - 0.6488 64.88%
PPAR gamma + 0.5222 52.22%
Honey bee toxicity - 0.7233 72.33%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity - 0.7627 76.27%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.99% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 95.51% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.27% 96.09%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 94.12% 94.23%
CHEMBL2581 P07339 Cathepsin D 92.25% 98.95%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 91.45% 94.08%
CHEMBL221 P23219 Cyclooxygenase-1 85.57% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 85.26% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.06% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.47% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.43% 96.00%
CHEMBL3902 P09211 Glutathione S-transferase Pi 81.70% 93.81%

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.
Camellia sinensis

Cross-Links

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PubChem 163075806
LOTUS LTS0010197
wikiData Q104976464