(8R,8'R)-Matairesinol 4,4'-di-O-beta-D-glucopyranoside

Details

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Internal ID 3857d199-f6cc-49f0-87fa-ea9e5dcb9a20
Taxonomy Lignans, neolignans and related compounds > Lignan glycosides
IUPAC Name (3R,4R)-3,4-bis[[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl]oxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H42O16/c1-42-20-9-14(3-5-18(20)45-31-28(39)26(37)24(35)22(11-33)47-31)7-16-13-44-30(41)17(16)8-15-4-6-19(21(10-15)43-2)46-32-29(40)27(38)25(36)23(12-34)48-32/h3-6,9-10,16-17,22-29,31-40H,7-8,11-13H2,1-2H3/t16-,17+,22+,23+,24+,25+,26-,27-,28+,29+,31+,32+/m0/s1
InChI Key UONVANCRWOWWAY-QFYIXHTHSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C32H42O16
Molecular Weight 682.70 g/mol
Exact Mass 682.24728525 g/mol
Topological Polar Surface Area (TPSA) 244.00 Ų
XlogP -0.30
Atomic LogP (AlogP) -2.36
H-Bond Acceptor 16
H-Bond Donor 8
Rotatable Bonds 12

Synonyms

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HY-156731
CS-0891681

2D Structure

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2D Structure of (8R,8'R)-Matairesinol 4,4'-di-O-beta-D-glucopyranoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6911 69.11%
Caco-2 - 0.8668 86.68%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7956 79.56%
OATP2B1 inhibitior - 0.8608 86.08%
OATP1B1 inhibitior + 0.8895 88.95%
OATP1B3 inhibitior + 0.9542 95.42%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.7878 78.78%
P-glycoprotein inhibitior + 0.6457 64.57%
P-glycoprotein substrate - 0.7165 71.65%
CYP3A4 substrate + 0.5860 58.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8578 85.78%
CYP3A4 inhibition - 0.6948 69.48%
CYP2C9 inhibition - 0.8615 86.15%
CYP2C19 inhibition - 0.7501 75.01%
CYP2D6 inhibition - 0.8975 89.75%
CYP1A2 inhibition - 0.8632 86.32%
CYP2C8 inhibition - 0.5856 58.56%
CYP inhibitory promiscuity - 0.6263 62.63%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6786 67.86%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9144 91.44%
Skin irritation - 0.8620 86.20%
Skin corrosion - 0.9628 96.28%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8222 82.22%
Micronuclear - 0.5500 55.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8596 85.96%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.7385 73.85%
Acute Oral Toxicity (c) III 0.7116 71.16%
Estrogen receptor binding + 0.7850 78.50%
Androgen receptor binding + 0.6099 60.99%
Thyroid receptor binding - 0.5087 50.87%
Glucocorticoid receptor binding + 0.5857 58.57%
Aromatase binding - 0.4946 49.46%
PPAR gamma + 0.7024 70.24%
Honey bee toxicity - 0.7720 77.20%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6749 67.49%
Fish aquatic toxicity + 0.9060 90.60%

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 98.20% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 97.59% 83.82%
CHEMBL2581 P07339 Cathepsin D 96.92% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.54% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.45% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.95% 94.45%
CHEMBL220 P22303 Acetylcholinesterase 90.14% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.87% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.52% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.87% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.78% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.86% 99.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.85% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.69% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.09% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 85.46% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.34% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.81% 97.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.77% 86.92%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.37% 97.14%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.19% 95.50%

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.
Trachelospermum asiaticum

Cross-Links

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PubChem 14608499
LOTUS LTS0062545
wikiData Q105276479