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

Details

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Internal ID 069fc006-a9ac-488f-ae3e-20d87a3038de
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 2-(hydroxymethyl)-6-(4-methylphenoxy)oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H18O6/c1-7-2-4-8(5-3-7)18-13-12(17)11(16)10(15)9(6-14)19-13/h2-5,9-17H,6H2,1H3
InChI Key MVLBSNPILSLTFZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C13H18O6
Molecular Weight 270.28 g/mol
Exact Mass 270.11033829 g/mol
Topological Polar Surface Area (TPSA) 99.40 Ų
XlogP 0.50
Atomic LogP (AlogP) -0.83
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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SCHEMBL24760381
AB00084039-01
SR-01000207893
SR-01000207893-1

2D Structure

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2D Structure of 2-(Hydroxymethyl)-6-(4-methylphenoxy)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 - 0.8305 83.05%
Caco-2 - 0.7437 74.37%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7167 71.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9477 94.77%
OATP1B3 inhibitior + 0.9565 95.65%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8777 87.77%
P-glycoprotein inhibitior - 0.9412 94.12%
P-glycoprotein substrate - 0.9860 98.60%
CYP3A4 substrate - 0.5654 56.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8250 82.50%
CYP3A4 inhibition - 0.8979 89.79%
CYP2C9 inhibition - 0.8918 89.18%
CYP2C19 inhibition - 0.9148 91.48%
CYP2D6 inhibition - 0.9455 94.55%
CYP1A2 inhibition - 0.9283 92.83%
CYP2C8 inhibition - 0.9032 90.32%
CYP inhibitory promiscuity - 0.6731 67.31%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6437 64.37%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.9242 92.42%
Skin irritation - 0.8449 84.49%
Skin corrosion - 0.9645 96.45%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5553 55.53%
Micronuclear - 0.5941 59.41%
Hepatotoxicity - 0.8000 80.00%
skin sensitisation - 0.8862 88.62%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.5851 58.51%
Acute Oral Toxicity (c) III 0.7517 75.17%
Estrogen receptor binding - 0.8381 83.81%
Androgen receptor binding - 0.6915 69.15%
Thyroid receptor binding - 0.6463 64.63%
Glucocorticoid receptor binding - 0.6156 61.56%
Aromatase binding - 0.8255 82.55%
PPAR gamma - 0.5369 53.69%
Honey bee toxicity - 0.9216 92.16%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6150 61.50%
Fish aquatic toxicity - 0.5188 51.88%

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 93.41% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.30% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 91.03% 94.73%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.65% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.36% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.11% 94.00%
CHEMBL2581 P07339 Cathepsin D 84.62% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.23% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.90% 96.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.83% 97.36%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.82% 95.89%

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.
Gymnadenia conopsea

Cross-Links

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PubChem 2844793
LOTUS LTS0173611
wikiData Q105173115