2-(Hydroxymethyl)-6-(2-methoxy-5-prop-2-enylphenoxy)oxane-3,4,5-triol

Details

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Internal ID e26c061f-cce7-4e55-8888-1e104b861d52
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 2-(hydroxymethyl)-6-(2-methoxy-5-prop-2-enylphenoxy)oxane-3,4,5-triol
SMILES (Canonical) COC1=C(C=C(C=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O
SMILES (Isomeric) COC1=C(C=C(C=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O
InChI InChI=1S/C16H22O7/c1-3-4-9-5-6-10(21-2)11(7-9)22-16-15(20)14(19)13(18)12(8-17)23-16/h3,5-7,12-20H,1,4,8H2,2H3
InChI Key LIEMWVYKRWIQMX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H22O7
Molecular Weight 326.34 g/mol
Exact Mass 326.13655304 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.40
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(Hydroxymethyl)-6-(2-methoxy-5-prop-2-enylphenoxy)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 - 0.7187 71.87%
Caco-2 - 0.7406 74.06%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.5526 55.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8953 89.53%
OATP1B3 inhibitior + 0.9742 97.42%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7998 79.98%
P-glycoprotein inhibitior - 0.9028 90.28%
P-glycoprotein substrate - 0.8365 83.65%
CYP3A4 substrate + 0.5204 52.04%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7725 77.25%
CYP3A4 inhibition - 0.5816 58.16%
CYP2C9 inhibition - 0.8254 82.54%
CYP2C19 inhibition - 0.7874 78.74%
CYP2D6 inhibition - 0.8948 89.48%
CYP1A2 inhibition - 0.8637 86.37%
CYP2C8 inhibition + 0.6538 65.38%
CYP inhibitory promiscuity - 0.5736 57.36%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7145 71.45%
Eye corrosion - 0.9869 98.69%
Eye irritation - 0.9669 96.69%
Skin irritation - 0.8139 81.39%
Skin corrosion - 0.9363 93.63%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4476 44.76%
Micronuclear - 0.5041 50.41%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation - 0.7773 77.73%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.7815 78.15%
Acute Oral Toxicity (c) III 0.7580 75.80%
Estrogen receptor binding - 0.6520 65.20%
Androgen receptor binding - 0.8013 80.13%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.5471 54.71%
Aromatase binding - 0.5150 51.50%
PPAR gamma + 0.5224 52.24%
Honey bee toxicity - 0.7622 76.22%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.7699 76.99%

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 97.70% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.68% 91.11%
CHEMBL3286 P00749 Urokinase-type plasminogen activator 94.85% 97.88%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.34% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.64% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.37% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.36% 86.33%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.00% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 83.97% 94.73%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.14% 86.92%
CHEMBL1255126 O15151 Protein Mdm4 82.58% 90.20%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.07% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.71% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.56% 95.56%

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.
Perilla frutescens

Cross-Links

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PubChem 73803891
LOTUS LTS0210812
wikiData Q105152148