Matairesinol 4'-O-b-gentiobioside

Details

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Internal ID 86c7717e-630f-447c-b66c-3ccef70f7c52
Taxonomy Lignans, neolignans and related compounds > Lignan glycosides
IUPAC Name 4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-[[3-methoxy-4-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]methyl]oxolan-2-one
SMILES (Canonical) COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)OC)O
SMILES (Isomeric) COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)OC)O
InChI InChI=1S/C32H42O16/c1-42-20-9-14(3-5-18(20)34)7-16-12-44-30(41)17(16)8-15-4-6-19(21(10-15)43-2)46-32-29(40)27(38)25(36)23(48-32)13-45-31-28(39)26(37)24(35)22(11-33)47-31/h3-6,9-10,16-17,22-29,31-40H,7-8,11-13H2,1-2H3
InChI Key SSZQYOJANKKXOX-UHFFFAOYSA-N
Popularity 0 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 -0.70
Atomic LogP (AlogP) -2.01
H-Bond Acceptor 16
H-Bond Donor 8
Rotatable Bonds 12

Synonyms

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106647-14-7
(3R-trans)-3-[[4-[(6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy]-3-methoxyphenyl]methyl]dihydro-4-[(4-hydroxy-3-methoxyphenyl)methyl]-2(3H)-furanone
4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-[[3-methoxy-4-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]methyl]oxolan-2-one
2(3H)-Furanone, 3-[[4-[(6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy]-3-methoxyphenyl]methyl]dihydro-4-[(4-hydroxy-3-methoxyphenyl)methyl]-, (3R-trans)-
AKOS040760546
Matairesinol 4??-O-??-D-glucopyranoside
FT-0775311

2D Structure

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2D Structure of Matairesinol 4'-O-b-gentiobioside

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 - 0.8876 88.76%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.7956 79.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8684 86.84%
OATP1B3 inhibitior + 0.9542 95.42%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.4525 45.25%
P-glycoprotein inhibitior + 0.6150 61.50%
P-glycoprotein substrate - 0.5825 58.25%
CYP3A4 substrate + 0.6285 62.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8559 85.59%
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 + 0.6146 61.46%
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 - 0.9205 92.05%
Skin irritation - 0.8620 86.20%
Skin corrosion - 0.9628 96.28%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7117 71.17%
Micronuclear - 0.5500 55.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.8596 85.96%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.7175 71.75%
Acute Oral Toxicity (c) III 0.7116 71.16%
Estrogen receptor binding + 0.7678 76.78%
Androgen receptor binding + 0.5825 58.25%
Thyroid receptor binding - 0.5390 53.90%
Glucocorticoid receptor binding + 0.5974 59.74%
Aromatase binding - 0.4875 48.75%
PPAR gamma + 0.6689 66.89%
Honey bee toxicity - 0.7614 76.14%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6549 65.49%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.09% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.04% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.42% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.25% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.27% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.61% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.07% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.48% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.40% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.03% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.35% 89.00%
CHEMBL220 P22303 Acetylcholinesterase 87.64% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 87.40% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.29% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.12% 97.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.85% 86.92%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.13% 96.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 82.53% 96.61%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.07% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.13% 95.50%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.10% 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.
Trachelospermum asiaticum

Cross-Links

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PubChem 73817506
LOTUS LTS0255466
wikiData Q105260049