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

Details

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Internal ID bc334dcd-81f1-4890-9181-24bc46cb2924
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 2-(hydroxymethyl)-6-(2-methoxy-4-propylphenoxy)oxane-3,4,5-triol
SMILES (Canonical) CCCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC
SMILES (Isomeric) CCCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC
InChI InChI=1S/C16H24O7/c1-3-4-9-5-6-10(11(7-9)21-2)22-16-15(20)14(19)13(18)12(8-17)23-16/h5-7,12-20H,3-4,8H2,1-2H3
InChI Key OEKQEDBCPPNGKO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H24O7
Molecular Weight 328.36 g/mol
Exact Mass 328.15220310 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 0.30
Atomic LogP (AlogP) -0.17
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-4-propylphenoxy)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 - 0.6671 66.71%
Caco-2 - 0.6657 66.57%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7492 74.92%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8695 86.95%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 0.9012 90.12%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7953 79.53%
P-glycoprotein inhibitior - 0.9240 92.40%
P-glycoprotein substrate - 0.7203 72.03%
CYP3A4 substrate + 0.5313 53.13%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7827 78.27%
CYP3A4 inhibition - 0.7699 76.99%
CYP2C9 inhibition - 0.6298 62.98%
CYP2C19 inhibition - 0.7419 74.19%
CYP2D6 inhibition - 0.8972 89.72%
CYP1A2 inhibition - 0.7068 70.68%
CYP2C8 inhibition + 0.7554 75.54%
CYP inhibitory promiscuity - 0.6774 67.74%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7280 72.80%
Eye corrosion - 0.9864 98.64%
Eye irritation - 0.9819 98.19%
Skin irritation - 0.8228 82.28%
Skin corrosion - 0.9454 94.54%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3905 39.05%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.8270 82.70%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.8206 82.06%
Acute Oral Toxicity (c) III 0.7772 77.72%
Estrogen receptor binding - 0.7106 71.06%
Androgen receptor binding - 0.7317 73.17%
Thyroid receptor binding - 0.5595 55.95%
Glucocorticoid receptor binding - 0.5726 57.26%
Aromatase binding - 0.7185 71.85%
PPAR gamma + 0.5197 51.97%
Honey bee toxicity - 0.8646 86.46%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6049 60.49%
Fish aquatic toxicity - 0.3917 39.17%

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 98.01% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.04% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.95% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.09% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.59% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.50% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.36% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.01% 92.62%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.07% 97.25%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.55% 86.92%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.01% 92.94%
CHEMBL3401 O75469 Pregnane X receptor 82.56% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.63% 96.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.47% 95.89%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.30% 100.00%

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.
Vitex glabrata

Cross-Links

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PubChem 13139862
LOTUS LTS0268190
wikiData Q105190340