[3,4,5-Triacetyloxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methyl acetate

Details

Top
Internal ID d001b5b8-0819-4ce1-b9c7-3e68f75b4a38
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name [3,4,5-triacetyloxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H30O13/c1-11(24)31-10-18-20(32-12(2)25)21(33-13(3)26)22(34-14(4)27)23(36-18)35-15-8-16(28-5)19(30-7)17(9-15)29-6/h8-9,18,20-23H,10H2,1-7H3
InChI Key NLKKHZDQGNSHOS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C23H30O13
Molecular Weight 514.50 g/mol
Exact Mass 514.16864101 g/mol
Topological Polar Surface Area (TPSA) 151.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.17
H-Bond Acceptor 13
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [3,4,5-Triacetyloxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methyl acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9616 96.16%
Caco-2 + 0.4901 49.01%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7979 79.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9073 90.73%
OATP1B3 inhibitior + 0.8849 88.49%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9361 93.61%
P-glycoprotein inhibitior + 0.8582 85.82%
P-glycoprotein substrate - 0.9434 94.34%
CYP3A4 substrate + 0.5667 56.67%
CYP2C9 substrate - 0.8042 80.42%
CYP2D6 substrate - 0.8707 87.07%
CYP3A4 inhibition - 0.8355 83.55%
CYP2C9 inhibition - 0.8287 82.87%
CYP2C19 inhibition - 0.6061 60.61%
CYP2D6 inhibition - 0.9024 90.24%
CYP1A2 inhibition + 0.6111 61.11%
CYP2C8 inhibition - 0.6052 60.52%
CYP inhibitory promiscuity + 0.5193 51.93%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.7078 70.78%
Eye corrosion - 0.9628 96.28%
Eye irritation - 0.8369 83.69%
Skin irritation - 0.8681 86.81%
Skin corrosion - 0.9819 98.19%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7377 73.77%
Micronuclear - 0.5575 55.75%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation - 0.8856 88.56%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.7294 72.94%
Acute Oral Toxicity (c) III 0.7116 71.16%
Estrogen receptor binding + 0.7550 75.50%
Androgen receptor binding - 0.6248 62.48%
Thyroid receptor binding + 0.5921 59.21%
Glucocorticoid receptor binding + 0.7323 73.23%
Aromatase binding - 0.4905 49.05%
PPAR gamma + 0.5827 58.27%
Honey bee toxicity - 0.8341 83.41%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5649 56.49%
Fish aquatic toxicity + 0.8817 88.17%

Targets

Top

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 98.22% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.55% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.41% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.09% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.76% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.39% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 87.39% 94.73%
CHEMBL4208 P20618 Proteasome component C5 86.91% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.47% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.75% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.26% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.56% 92.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.00% 95.89%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.95% 94.80%
CHEMBL5255 O00206 Toll-like receptor 4 82.44% 92.50%
CHEMBL340 P08684 Cytochrome P450 3A4 81.64% 91.19%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.39% 89.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.46% 97.21%

Plants that contains it

Top
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.
Rosa transmorrisonensis

Cross-Links

Top
PubChem 13922635
LOTUS LTS0115161
wikiData Q105181393