(-)-phenylethyl-8-O-alpha-L-rhamnopyranoside

Details

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Internal ID dfd9b1f0-7c97-4a27-8c99-d1378ecf72d4
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (2S,3R,4R,5R,6R)-2-methyl-6-(2-phenylethoxy)oxane-3,4,5-triol
SMILES (Canonical) CC1C(C(C(C(O1)OCCC2=CC=CC=C2)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OCCC2=CC=CC=C2)O)O)O
InChI InChI=1S/C14H20O5/c1-9-11(15)12(16)13(17)14(19-9)18-8-7-10-5-3-2-4-6-10/h2-6,9,11-17H,7-8H2,1H3/t9-,11-,12+,13+,14+/m0/s1
InChI Key YUDRGFQOIGCZAM-DDNMXHNFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H20O5
Molecular Weight 268.30 g/mol
Exact Mass 268.13107373 g/mol
Topological Polar Surface Area (TPSA) 79.20 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.07
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (-)-phenylethyl-8-O-alpha-L-rhamnopyranoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8750 87.50%
Caco-2 + 0.6107 61.07%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8352 83.52%
OATP2B1 inhibitior - 0.8622 86.22%
OATP1B1 inhibitior + 0.9164 91.64%
OATP1B3 inhibitior + 0.9377 93.77%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9558 95.58%
P-glycoprotein inhibitior - 0.9294 92.94%
P-glycoprotein substrate - 0.9001 90.01%
CYP3A4 substrate - 0.5547 55.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7915 79.15%
CYP3A4 inhibition - 0.8267 82.67%
CYP2C9 inhibition - 0.7078 70.78%
CYP2C19 inhibition - 0.8135 81.35%
CYP2D6 inhibition - 0.9184 91.84%
CYP1A2 inhibition - 0.8711 87.11%
CYP2C8 inhibition + 0.4894 48.94%
CYP inhibitory promiscuity - 0.6639 66.39%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6648 66.48%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.9066 90.66%
Skin irritation - 0.8196 81.96%
Skin corrosion - 0.9528 95.28%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6950 69.50%
Micronuclear - 0.7382 73.82%
Hepatotoxicity - 0.6964 69.64%
skin sensitisation - 0.8890 88.90%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.8040 80.40%
Acute Oral Toxicity (c) III 0.7536 75.36%
Estrogen receptor binding - 0.7921 79.21%
Androgen receptor binding - 0.7822 78.22%
Thyroid receptor binding - 0.5114 51.14%
Glucocorticoid receptor binding - 0.6337 63.37%
Aromatase binding - 0.7361 73.61%
PPAR gamma - 0.5284 52.84%
Honey bee toxicity - 0.8768 87.68%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity - 0.6340 63.40%

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 96.06% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.30% 98.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 94.62% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.37% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.46% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 92.03% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 85.75% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.25% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 101904449
LOTUS LTS0264069
wikiData Q77566201