[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-2-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate

Details

Top
Internal ID da40b60e-6a3a-4e6e-aea2-a447b2fa3a5e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Oligosaccharides
IUPAC Name [6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C35H46O20/c1-14-24(43)26(45)28(47)33(50-14)54-31-30(53-23(42)7-4-15-2-5-17(38)19(40)10-15)22(13-37)52-35(49-9-8-16-3-6-18(39)20(41)11-16)32(31)55-34-29(48)27(46)25(44)21(12-36)51-34/h2-7,10-11,14,21-22,24-41,43-48H,8-9,12-13H2,1H3
InChI Key LKZNLGSMAMRYPE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C35H46O20
Molecular Weight 786.70 g/mol
Exact Mass 786.25824385 g/mol
Topological Polar Surface Area (TPSA) 324.00 Ų
XlogP -2.10
Atomic LogP (AlogP) -3.19
H-Bond Acceptor 20
H-Bond Donor 12
Rotatable Bonds 13

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [6-[2-(3,4-Dihydroxyphenyl)ethoxy]-2-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7512 75.12%
Caco-2 - 0.9016 90.16%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.8857 88.57%
Subcellular localzation Mitochondria 0.7836 78.36%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.8704 87.04%
OATP1B3 inhibitior + 0.9632 96.32%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8562 85.62%
P-glycoprotein inhibitior - 0.4679 46.79%
P-glycoprotein substrate - 0.6270 62.70%
CYP3A4 substrate + 0.6511 65.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8696 86.96%
CYP3A4 inhibition - 0.9295 92.95%
CYP2C9 inhibition - 0.7548 75.48%
CYP2C19 inhibition - 0.8660 86.60%
CYP2D6 inhibition - 0.9109 91.09%
CYP1A2 inhibition - 0.8666 86.66%
CYP2C8 inhibition + 0.6998 69.98%
CYP inhibitory promiscuity - 0.7002 70.02%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6737 67.37%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.9162 91.62%
Skin irritation - 0.8386 83.86%
Skin corrosion - 0.9560 95.60%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7396 73.96%
Micronuclear - 0.6567 65.67%
Hepatotoxicity - 0.9375 93.75%
skin sensitisation - 0.8442 84.42%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.9541 95.41%
Acute Oral Toxicity (c) III 0.7702 77.02%
Estrogen receptor binding + 0.7766 77.66%
Androgen receptor binding - 0.7155 71.55%
Thyroid receptor binding + 0.5366 53.66%
Glucocorticoid receptor binding - 0.4653 46.53%
Aromatase binding + 0.5284 52.84%
PPAR gamma + 0.7134 71.34%
Honey bee toxicity - 0.6926 69.26%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.7970 79.70%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.64% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.56% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.42% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.13% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.57% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.19% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 93.95% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.23% 99.17%
CHEMBL2581 P07339 Cathepsin D 92.78% 98.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 92.01% 86.92%
CHEMBL3194 P02766 Transthyretin 92.01% 90.71%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 88.03% 80.78%
CHEMBL3714130 P46095 G-protein coupled receptor 6 86.55% 97.36%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 84.17% 96.37%
CHEMBL4208 P20618 Proteasome component C5 82.90% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.61% 94.45%
CHEMBL226 P30542 Adenosine A1 receptor 82.60% 95.93%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.78% 91.71%

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.
Veronica pectinata

Cross-Links

Top
PubChem 85143867
LOTUS LTS0266190
wikiData Q105153365