(3R,3aR,6aR)-3-[4-[1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-3,3a,4,6a-tetrahydro-1H-furo[3,4-c]furan-6-one

Details

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Internal ID 32fea2bb-cd16-4cdc-95d4-0623e8d33f17
Taxonomy Lignans, neolignans and related compounds > Lignan lactones
IUPAC Name (3R,3aR,6aR)-3-[4-[1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-3,3a,4,6a-tetrahydro-1H-furo[3,4-c]furan-6-one
SMILES (Canonical) COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3C4COC(=O)C4CO3
SMILES (Isomeric) COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)[C@H]3[C@H]4COC(=O)[C@H]4CO3
InChI InChI=1S/C24H28O10/c1-29-17-6-12(4-5-16(17)26)21(27)20(9-25)34-23-18(30-2)7-13(8-19(23)31-3)22-14-10-33-24(28)15(14)11-32-22/h4-8,14-15,20-22,25-27H,9-11H2,1-3H3/t14-,15-,20?,21?,22-/m0/s1
InChI Key WXNHVUOGFJILRR-YGAXPAPJSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H28O10
Molecular Weight 476.50 g/mol
Exact Mass 476.16824709 g/mol
Topological Polar Surface Area (TPSA) 133.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.75
H-Bond Acceptor 10
H-Bond Donor 3
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,3aR,6aR)-3-[4-[1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-3,3a,4,6a-tetrahydro-1H-furo[3,4-c]furan-6-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9454 94.54%
Caco-2 - 0.5712 57.12%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7549 75.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8984 89.84%
OATP1B3 inhibitior + 0.9088 90.88%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.5629 56.29%
P-glycoprotein inhibitior + 0.7562 75.62%
P-glycoprotein substrate - 0.6258 62.58%
CYP3A4 substrate + 0.6000 60.00%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.7633 76.33%
CYP3A4 inhibition - 0.6254 62.54%
CYP2C9 inhibition - 0.6343 63.43%
CYP2C19 inhibition - 0.6300 63.00%
CYP2D6 inhibition - 0.9434 94.34%
CYP1A2 inhibition - 0.8608 86.08%
CYP2C8 inhibition - 0.5763 57.63%
CYP inhibitory promiscuity + 0.6109 61.09%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6003 60.03%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.8867 88.67%
Skin irritation - 0.8636 86.36%
Skin corrosion - 0.9682 96.82%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6154 61.54%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.8350 83.50%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.8469 84.69%
Acute Oral Toxicity (c) III 0.6239 62.39%
Estrogen receptor binding + 0.8277 82.77%
Androgen receptor binding + 0.7671 76.71%
Thyroid receptor binding + 0.6635 66.35%
Glucocorticoid receptor binding + 0.7636 76.36%
Aromatase binding - 0.6605 66.05%
PPAR gamma + 0.6003 60.03%
Honey bee toxicity - 0.7795 77.95%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9572 95.72%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.51% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.25% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.84% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.28% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.75% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.64% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.29% 99.15%
CHEMBL2535 P11166 Glucose transporter 89.78% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.37% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.32% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.29% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.22% 99.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.17% 89.62%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.93% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.84% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.11% 92.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.65% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.16% 94.00%
CHEMBL204 P00734 Thrombin 82.05% 96.01%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.76% 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.
Tarenna attenuata

Cross-Links

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PubChem 16216276
LOTUS LTS0119600
wikiData Q105314773