(1S,2R)-2-[5-[(3R,3aS,6R,6aS)-6-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol

Details

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Internal ID 6195f2a0-5711-4c2a-8a94-2edaa7192d55
Taxonomy Lignans, neolignans and related compounds > Furanoid lignans
IUPAC Name (1S,2R)-2-[5-[(3R,3aS,6R,6aS)-6-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol
SMILES (Canonical) COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC)OC(CO)C(C5=CC(=C(C=C5)O)OC)O
SMILES (Isomeric) COC1=C(C=C(C=C1)[C@H]2[C@@H]3CO[C@H]([C@@H]3CO2)C4=CC(=C(C(=C4)OC)O)OC)O[C@H](CO)[C@H](C5=CC(=C(C=C5)O)OC)O
InChI InChI=1S/C31H36O11/c1-36-22-8-6-17(10-24(22)42-27(13-32)28(34)16-5-7-21(33)23(9-16)37-2)30-19-14-41-31(20(19)15-40-30)18-11-25(38-3)29(35)26(12-18)39-4/h5-12,19-20,27-28,30-35H,13-15H2,1-4H3/t19-,20-,27-,28+,30+,31+/m1/s1
InChI Key GWAGNJOOCODQGM-VSXYQEGNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H36O11
Molecular Weight 584.60 g/mol
Exact Mass 584.22576196 g/mol
Topological Polar Surface Area (TPSA) 146.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 3.68
H-Bond Acceptor 11
H-Bond Donor 4
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,2R)-2-[5-[(3R,3aS,6R,6aS)-6-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9551 95.51%
Caco-2 - 0.8099 80.99%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7419 74.19%
OATP2B1 inhibitior - 0.8572 85.72%
OATP1B1 inhibitior + 0.8762 87.62%
OATP1B3 inhibitior + 0.9399 93.99%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.7937 79.37%
P-glycoprotein inhibitior + 0.7628 76.28%
P-glycoprotein substrate - 0.5201 52.01%
CYP3A4 substrate + 0.5755 57.55%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate + 0.4103 41.03%
CYP3A4 inhibition - 0.6110 61.10%
CYP2C9 inhibition - 0.6315 63.15%
CYP2C19 inhibition - 0.5539 55.39%
CYP2D6 inhibition - 0.9114 91.14%
CYP1A2 inhibition - 0.7664 76.64%
CYP2C8 inhibition + 0.4696 46.96%
CYP inhibitory promiscuity + 0.7224 72.24%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5644 56.44%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9010 90.10%
Skin irritation - 0.8466 84.66%
Skin corrosion - 0.9618 96.18%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7055 70.55%
Micronuclear + 0.6100 61.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation - 0.8150 81.50%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.9573 95.73%
Acute Oral Toxicity (c) III 0.6511 65.11%
Estrogen receptor binding + 0.8583 85.83%
Androgen receptor binding + 0.7254 72.54%
Thyroid receptor binding + 0.6588 65.88%
Glucocorticoid receptor binding + 0.7296 72.96%
Aromatase binding + 0.5595 55.95%
PPAR gamma + 0.6807 68.07%
Honey bee toxicity - 0.8696 86.96%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.8938 89.38%

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 99.28% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.22% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.77% 85.14%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 95.42% 89.62%
CHEMBL2581 P07339 Cathepsin D 94.28% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.78% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.04% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.93% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.43% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.51% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.09% 89.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 85.49% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.88% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.61% 99.17%
CHEMBL4208 P20618 Proteasome component C5 84.60% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.16% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.83% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.22% 92.62%
CHEMBL3438 Q05513 Protein kinase C zeta 80.90% 88.48%

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.
Dysoxylum densiflorum
Ficus microcarpa

Cross-Links

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PubChem 162896454
LOTUS LTS0052185
wikiData Q105022113