2-(2,4-Dihydroxy-6-methylphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID 9686b861-d818-4a53-83b5-6007deb010db
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 2-(2,4-dihydroxy-6-methylphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H18O8/c1-5-2-6(15)3-7(16)12(5)21-13-11(19)10(18)9(17)8(4-14)20-13/h2-3,8-11,13-19H,4H2,1H3
InChI Key CVVMLCYWLCXJCW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18O8
Molecular Weight 302.28 g/mol
Exact Mass 302.10016753 g/mol
Topological Polar Surface Area (TPSA) 140.00 Ų
XlogP -0.60
Atomic LogP (AlogP) -1.42
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(2,4-Dihydroxy-6-methylphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7883 78.83%
Caco-2 - 0.8695 86.95%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.6869 68.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9266 92.66%
OATP1B3 inhibitior + 0.9524 95.24%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9374 93.74%
P-glycoprotein inhibitior - 0.9319 93.19%
P-glycoprotein substrate - 0.9679 96.79%
CYP3A4 substrate - 0.5194 51.94%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.8226 82.26%
CYP3A4 inhibition - 0.8855 88.55%
CYP2C9 inhibition - 0.8536 85.36%
CYP2C19 inhibition - 0.8888 88.88%
CYP2D6 inhibition - 0.9405 94.05%
CYP1A2 inhibition - 0.8949 89.49%
CYP2C8 inhibition - 0.6586 65.86%
CYP inhibitory promiscuity - 0.6397 63.97%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6897 68.97%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9168 91.68%
Skin irritation - 0.8327 83.27%
Skin corrosion - 0.9554 95.54%
Ames mutagenesis - 0.7454 74.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4506 45.06%
Micronuclear - 0.5382 53.82%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.8377 83.77%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.6765 67.65%
Acute Oral Toxicity (c) III 0.7581 75.81%
Estrogen receptor binding - 0.6345 63.45%
Androgen receptor binding - 0.6823 68.23%
Thyroid receptor binding + 0.5978 59.78%
Glucocorticoid receptor binding - 0.5371 53.71%
Aromatase binding - 0.7609 76.09%
PPAR gamma + 0.5467 54.67%
Honey bee toxicity - 0.8531 85.31%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity - 0.4415 44.15%

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 97.89% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 92.79% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.03% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.78% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.02% 94.00%
CHEMBL2581 P07339 Cathepsin D 86.47% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.92% 89.00%
CHEMBL4208 P20618 Proteasome component C5 84.82% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.62% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.43% 86.33%

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.
Myrsine africana

Cross-Links

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PubChem 163081326
LOTUS LTS0036104
wikiData Q104971032