(6-Ethoxy-3,4,5-trihydroxyoxan-2-yl)methyl 2-phenylpropanoate

Details

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Internal ID 5bf4ca43-7658-4e96-b571-9d19d4df7dc8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (6-ethoxy-3,4,5-trihydroxyoxan-2-yl)methyl 2-phenylpropanoate
SMILES (Canonical) CCOC1C(C(C(C(O1)COC(=O)C(C)C2=CC=CC=C2)O)O)O
SMILES (Isomeric) CCOC1C(C(C(C(O1)COC(=O)C(C)C2=CC=CC=C2)O)O)O
InChI InChI=1S/C17H24O7/c1-3-22-17-15(20)14(19)13(18)12(24-17)9-23-16(21)10(2)11-7-5-4-6-8-11/h4-8,10,12-15,17-20H,3,9H2,1-2H3
InChI Key FLQWBRLRHIJJEN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H24O7
Molecular Weight 340.40 g/mol
Exact Mass 340.15220310 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.18
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6-Ethoxy-3,4,5-trihydroxyoxan-2-yl)methyl 2-phenylpropanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7556 75.56%
Caco-2 - 0.7668 76.68%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8117 81.17%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9070 90.70%
OATP1B3 inhibitior + 0.9311 93.11%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7002 70.02%
P-glycoprotein inhibitior - 0.7955 79.55%
P-glycoprotein substrate - 0.9553 95.53%
CYP3A4 substrate - 0.5302 53.02%
CYP2C9 substrate - 0.8096 80.96%
CYP2D6 substrate - 0.8875 88.75%
CYP3A4 inhibition - 0.8852 88.52%
CYP2C9 inhibition - 0.7866 78.66%
CYP2C19 inhibition - 0.8438 84.38%
CYP2D6 inhibition - 0.9344 93.44%
CYP1A2 inhibition - 0.8518 85.18%
CYP2C8 inhibition - 0.9044 90.44%
CYP inhibitory promiscuity - 0.6583 65.83%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6856 68.56%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.9689 96.89%
Skin irritation - 0.8633 86.33%
Skin corrosion - 0.9662 96.62%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6217 62.17%
Micronuclear - 0.6026 60.26%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8968 89.68%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.8034 80.34%
Acute Oral Toxicity (c) III 0.7257 72.57%
Estrogen receptor binding + 0.5468 54.68%
Androgen receptor binding - 0.5845 58.45%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.6157 61.57%
Aromatase binding - 0.6430 64.30%
PPAR gamma - 0.4882 48.82%
Honey bee toxicity - 0.8801 88.01%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6155 61.55%
Fish aquatic toxicity + 0.7204 72.04%

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 97.16% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 96.70% 90.17%
CHEMBL2581 P07339 Cathepsin D 95.26% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 93.06% 94.73%
CHEMBL218 P21554 Cannabinoid CB1 receptor 88.11% 96.61%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.06% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.37% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.65% 96.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.36% 96.47%
CHEMBL4040 P28482 MAP kinase ERK2 85.27% 83.82%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.69% 93.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.01% 86.33%
CHEMBL5028 O14672 ADAM10 83.79% 97.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.75% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.18% 95.50%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.19% 97.25%

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.
Nicotiana tabacum

Cross-Links

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PubChem 162903642
LOTUS LTS0167352
wikiData Q104997374