(2R,3S,4S)-3a-[(beta-D-glucopyranosyl)oxy]lyoniresinol

Details

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Internal ID 0b113e6e-f62e-4d7b-ae13-3cffda85b2d2
Taxonomy Lignans, neolignans and related compounds > Lignan glycosides
IUPAC Name (2R,3R,4S,5S,6R)-2-[[(1S,2S,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(C(O4)CO)O)O)O
SMILES (Isomeric) COC1=CC(=CC(=C1O)OC)[C@@H]2[C@@H]([C@@H](CC3=CC(=C(C(=C23)OC)O)OC)CO)CO[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
InChI InChI=1S/C28H38O13/c1-36-16-7-13(8-17(37-2)22(16)31)20-15(11-40-28-26(35)25(34)23(32)19(10-30)41-28)14(9-29)5-12-6-18(38-3)24(33)27(39-4)21(12)20/h6-8,14-15,19-20,23,25-26,28-35H,5,9-11H2,1-4H3/t14-,15+,19+,20+,23+,25-,26+,28+/m0/s1
InChI Key PQQRNPDHSJDAGV-OOMNAYAOSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C28H38O13
Molecular Weight 582.60 g/mol
Exact Mass 582.23124126 g/mol
Topological Polar Surface Area (TPSA) 197.00 Ų
XlogP 0.40
Atomic LogP (AlogP) -0.14
H-Bond Acceptor 13
H-Bond Donor 7
Rotatable Bonds 10

Synonyms

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CHEBI:67412
(2R,3S,4S)-3a-[(beta-D-glucopyranosyl)oxy]lyoniresinol
BDBM50349825
Q27135874
[(1S)-1alpha-(3,5-Dimethoxy-4-hydroxyphenyl)-3alpha-(hydroxymethyl)-6,8-dimethoxy-7-hydroxytetralin-2alpha-yl]methyl beta-D-glucopyranoside

2D Structure

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2D Structure of (2R,3S,4S)-3a-[(beta-D-glucopyranosyl)oxy]lyoniresinol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5464 54.64%
Caco-2 - 0.8381 83.81%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5820 58.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8192 81.92%
OATP1B3 inhibitior + 0.9597 95.97%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.5855 58.55%
P-glycoprotein inhibitior - 0.5097 50.97%
P-glycoprotein substrate - 0.6938 69.38%
CYP3A4 substrate + 0.5958 59.58%
CYP2C9 substrate - 0.8002 80.02%
CYP2D6 substrate - 0.7492 74.92%
CYP3A4 inhibition - 0.9149 91.49%
CYP2C9 inhibition - 0.8886 88.86%
CYP2C19 inhibition - 0.8106 81.06%
CYP2D6 inhibition - 0.9246 92.46%
CYP1A2 inhibition - 0.7947 79.47%
CYP2C8 inhibition + 0.5498 54.98%
CYP inhibitory promiscuity - 0.6489 64.89%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6531 65.31%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9184 91.84%
Skin irritation - 0.8512 85.12%
Skin corrosion - 0.9600 96.00%
Ames mutagenesis - 0.6154 61.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7592 75.92%
Micronuclear + 0.6059 60.59%
Hepatotoxicity - 0.8000 80.00%
skin sensitisation - 0.9256 92.56%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.9178 91.78%
Acute Oral Toxicity (c) III 0.6648 66.48%
Estrogen receptor binding + 0.8080 80.80%
Androgen receptor binding + 0.6649 66.49%
Thyroid receptor binding + 0.5682 56.82%
Glucocorticoid receptor binding + 0.6258 62.58%
Aromatase binding + 0.5696 56.96%
PPAR gamma + 0.6064 60.64%
Honey bee toxicity - 0.7973 79.73%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.8364 83.64%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.60% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.68% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.13% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.47% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.36% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.68% 99.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.13% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.51% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.86% 89.62%
CHEMBL2581 P07339 Cathepsin D 86.38% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.18% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.05% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.53% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.02% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.86% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.31% 95.89%

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.
Annona squamosa
Arcangelisia gusanlung

Cross-Links

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PubChem 56671845
NPASS NPC145979
LOTUS LTS0108072
wikiData Q27135874