2-(6-Ethoxy-4-methoxy-2-methyloxan-3-yl)oxy-4-methoxy-6-methyloxane-3,5-diol

Details

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Internal ID 22ed4755-049f-471a-b341-e98a8c04aae1
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name 2-(6-ethoxy-4-methoxy-2-methyloxan-3-yl)oxy-4-methoxy-6-methyloxane-3,5-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H30O8/c1-6-21-11-7-10(19-4)14(9(3)22-11)24-16-13(18)15(20-5)12(17)8(2)23-16/h8-18H,6-7H2,1-5H3
InChI Key LYTHASQZLYCEJZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H30O8
Molecular Weight 350.40 g/mol
Exact Mass 350.19406791 g/mol
Topological Polar Surface Area (TPSA) 95.80 Ų
XlogP -0.20
Atomic LogP (AlogP) 0.04
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(6-Ethoxy-4-methoxy-2-methyloxan-3-yl)oxy-4-methoxy-6-methyloxane-3,5-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5636 56.36%
Caco-2 - 0.5885 58.85%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6958 69.58%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9369 93.69%
OATP1B3 inhibitior + 0.8578 85.78%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7896 78.96%
P-glycoprotein inhibitior - 0.8552 85.52%
P-glycoprotein substrate - 0.7007 70.07%
CYP3A4 substrate + 0.5901 59.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8209 82.09%
CYP3A4 inhibition - 0.8528 85.28%
CYP2C9 inhibition - 0.8873 88.73%
CYP2C19 inhibition - 0.8193 81.93%
CYP2D6 inhibition - 0.9070 90.70%
CYP1A2 inhibition - 0.9294 92.94%
CYP2C8 inhibition - 0.8999 89.99%
CYP inhibitory promiscuity - 0.7294 72.94%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6596 65.96%
Eye corrosion - 0.9852 98.52%
Eye irritation - 0.9389 93.89%
Skin irritation - 0.8394 83.94%
Skin corrosion - 0.9703 97.03%
Ames mutagenesis - 0.5954 59.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6169 61.69%
Micronuclear - 0.6526 65.26%
Hepatotoxicity - 0.5895 58.95%
skin sensitisation - 0.8807 88.07%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.6104 61.04%
Acute Oral Toxicity (c) III 0.7961 79.61%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.7953 79.53%
Thyroid receptor binding + 0.7830 78.30%
Glucocorticoid receptor binding - 0.6192 61.92%
Aromatase binding + 0.5300 53.00%
PPAR gamma - 0.5299 52.99%
Honey bee toxicity - 0.7135 71.35%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity - 0.4894 48.94%

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 96.04% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.47% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 88.04% 95.93%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.49% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.80% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.50% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.00% 97.25%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.67% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.01% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.68% 99.17%
CHEMBL2581 P07339 Cathepsin D 80.53% 98.95%

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.
Solanum nigrum

Cross-Links

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PubChem 162949578
LOTUS LTS0194934
wikiData Q105159555