[(2R,3R)-4-(3,5-Dimethoxy-4-hydroxyphenyl)-3-(hydroxymethyl)-2-(3,5-dimethoxy-4-hydroxybenzyl)butyl]beta-D-xylopyranoside

Details

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Internal ID 18e9a9cd-903d-475f-8832-890172ef9d56
Taxonomy Lignans, neolignans and related compounds > Lignan glycosides
IUPAC Name (2R,3R,4S,5R)-2-[(2S,3S)-4-hydroxy-2,3-bis[(4-hydroxy-3,5-dimethoxyphenyl)methyl]butoxy]oxane-3,4,5-triol
SMILES (Canonical) COC1=CC(=CC(=C1O)OC)CC(CO)C(CC2=CC(=C(C(=C2)OC)O)OC)COC3C(C(C(CO3)O)O)O
SMILES (Isomeric) COC1=CC(=CC(=C1O)OC)C[C@H](CO)[C@H](CC2=CC(=C(C(=C2)OC)O)OC)CO[C@H]3[C@@H]([C@H]([C@@H](CO3)O)O)O
InChI InChI=1S/C27H38O12/c1-34-19-7-14(8-20(35-2)24(19)31)5-16(11-28)17(12-38-27-26(33)23(30)18(29)13-39-27)6-15-9-21(36-3)25(32)22(10-15)37-4/h7-10,16-18,23,26-33H,5-6,11-13H2,1-4H3/t16-,17-,18-,23+,26-,27-/m1/s1
InChI Key UTPBCUCEDIRSFI-KHLXKNNCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H38O12
Molecular Weight 554.60 g/mol
Exact Mass 554.23632664 g/mol
Topological Polar Surface Area (TPSA) 177.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.60
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 13

Synonyms

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126882-53-9
[(2R,3R)-4-(3,5-Dimethoxy-4-hydroxyphenyl)-3-(hydroxymethyl)-2-(3,5-dimethoxy-4-hydroxybenzyl)butyl]beta-D-xylopyranoside
DTXSID001318511
HY-N1216
AKOS032962317
CS-0016603

2D Structure

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2D Structure of [(2R,3R)-4-(3,5-Dimethoxy-4-hydroxyphenyl)-3-(hydroxymethyl)-2-(3,5-dimethoxy-4-hydroxybenzyl)butyl]beta-D-xylopyranoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7356 73.56%
Caco-2 - 0.8119 81.19%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6717 67.17%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8305 83.05%
OATP1B3 inhibitior + 0.9442 94.42%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6760 67.60%
P-glycoprotein inhibitior + 0.6162 61.62%
P-glycoprotein substrate + 0.5269 52.69%
CYP3A4 substrate + 0.5924 59.24%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.7750 77.50%
CYP3A4 inhibition - 0.8652 86.52%
CYP2C9 inhibition - 0.9201 92.01%
CYP2C19 inhibition - 0.8847 88.47%
CYP2D6 inhibition - 0.8936 89.36%
CYP1A2 inhibition - 0.8508 85.08%
CYP2C8 inhibition + 0.4880 48.80%
CYP inhibitory promiscuity - 0.8964 89.64%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7129 71.29%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.9237 92.37%
Skin irritation - 0.8601 86.01%
Skin corrosion - 0.9638 96.38%
Ames mutagenesis + 0.6356 63.56%
Human Ether-a-go-go-Related Gene inhibition + 0.6906 69.06%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.8891 88.91%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.9470 94.70%
Acute Oral Toxicity (c) III 0.7365 73.65%
Estrogen receptor binding + 0.7860 78.60%
Androgen receptor binding + 0.5868 58.68%
Thyroid receptor binding + 0.5719 57.19%
Glucocorticoid receptor binding + 0.5561 55.61%
Aromatase binding + 0.5261 52.61%
PPAR gamma + 0.5479 54.79%
Honey bee toxicity - 0.7899 78.99%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6749 67.49%
Fish aquatic toxicity + 0.7983 79.83%

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 98.35% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.82% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.75% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 92.11% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.42% 99.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 89.35% 95.89%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 88.62% 95.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.56% 89.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.74% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.49% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.08% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.06% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.98% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.34% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.84% 94.00%
CHEMBL2535 P11166 Glucose transporter 82.56% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.45% 96.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.43% 97.14%

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.
Litsea glutinosa
Prunus padus

Cross-Links

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PubChem 14521029
LOTUS LTS0099446
wikiData Q105278955