(2S,3R,6S)-2-(Hydroxy(4-Hydroxy-3,5-Dimethoxyphenyl)Methyl)-3-(5-Methoxy-3,4-Methylenedioxybenzyl)Butyrolactone

Details

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Internal ID abd2f3a7-eaea-4195-ac13-0b5e46bd2bfb
Taxonomy Lignans, neolignans and related compounds > Furanoid lignans > Tetrahydrofuran lignans > 9,9-epoxylignans > Dibenzylbutyrolactone lignans
IUPAC Name (3S,4R)-3-[(S)-hydroxy-(4-hydroxy-3,5-dimethoxyphenyl)methyl]-4-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]oxolan-2-one
SMILES (Canonical) COC1=CC(=CC2=C1OCO2)CC3COC(=O)C3C(C4=CC(=C(C(=C4)OC)O)OC)O
SMILES (Isomeric) COC1=CC(=CC2=C1OCO2)C[C@H]3COC(=O)[C@@H]3[C@@H](C4=CC(=C(C(=C4)OC)O)OC)O
InChI InChI=1S/C22H24O9/c1-26-14-7-12(8-15(27-2)20(14)24)19(23)18-13(9-29-22(18)25)4-11-5-16(28-3)21-17(6-11)30-10-31-21/h5-8,13,18-19,23-24H,4,9-10H2,1-3H3/t13-,18-,19+/m0/s1
InChI Key JUFCGVIVUSQKEM-FASAQXTFSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H24O9
Molecular Weight 432.40 g/mol
Exact Mass 432.14203234 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.21
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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(2S,3R,6S)-2-[Hydroxy(4-hydroxy-3,5-dimethoxyphenyl)methyl]-3-(5-methoxy-3,4-methylenedioxybenzyl)butyrolactone
InChI=1/C22H24O9/c1-26-14-7-12(8-15(27-2)20(14)24)19(23)18-13(9-29-22(18)25)4-11-5-16(28-3)21-17(6-11)30-10-31-21/h5-8,13,18-19,23-24H,4,9-10H2,1-3H3/t13-,18-,19?/m0/s

2D Structure

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2D Structure of (2S,3R,6S)-2-(Hydroxy(4-Hydroxy-3,5-Dimethoxyphenyl)Methyl)-3-(5-Methoxy-3,4-Methylenedioxybenzyl)Butyrolactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9116 91.16%
Caco-2 - 0.5150 51.50%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7407 74.07%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8399 83.99%
OATP1B3 inhibitior + 0.9008 90.08%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.7379 73.79%
P-glycoprotein inhibitior + 0.6711 67.11%
P-glycoprotein substrate + 0.5081 50.81%
CYP3A4 substrate + 0.6007 60.07%
CYP2C9 substrate - 0.6043 60.43%
CYP2D6 substrate - 0.7539 75.39%
CYP3A4 inhibition + 0.6593 65.93%
CYP2C9 inhibition + 0.8760 87.60%
CYP2C19 inhibition + 0.8584 85.84%
CYP2D6 inhibition - 0.6165 61.65%
CYP1A2 inhibition - 0.7985 79.85%
CYP2C8 inhibition - 0.6266 62.66%
CYP inhibitory promiscuity + 0.8922 89.22%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4386 43.86%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.8867 88.67%
Skin irritation - 0.8177 81.77%
Skin corrosion - 0.9655 96.55%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4355 43.55%
Micronuclear + 0.7074 70.74%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.7799 77.99%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.8142 81.42%
Acute Oral Toxicity (c) III 0.6194 61.94%
Estrogen receptor binding + 0.9039 90.39%
Androgen receptor binding + 0.6163 61.63%
Thyroid receptor binding + 0.6880 68.80%
Glucocorticoid receptor binding + 0.7745 77.45%
Aromatase binding - 0.6082 60.82%
PPAR gamma + 0.6691 66.91%
Honey bee toxicity - 0.6554 65.54%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9466 94.66%

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 99.37% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 98.61% 83.82%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.51% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.26% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.75% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.03% 94.45%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 94.97% 92.62%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.73% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.06% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.98% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 87.51% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.40% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.20% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.15% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.07% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.04% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.60% 96.00%
CHEMBL4208 P20618 Proteasome component C5 84.21% 90.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.20% 97.09%
CHEMBL204 P00734 Thrombin 81.52% 96.01%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.16% 89.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.67% 94.00%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.60% 89.50%

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.
Peperomia heyneana

Cross-Links

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PubChem 11690564
LOTUS LTS0146244
wikiData Q105135192