(3E,4S)-4-(1,3-benzodioxol-5-ylmethyl)-3-(1,3-benzodioxol-5-ylmethylidene)-4-hydroxyoxolan-2-one

Details

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Internal ID 9faffb24-d3e1-4238-9a9f-235e34f82d41
Taxonomy Lignans, neolignans and related compounds > Furanoid lignans > Tetrahydrofuran lignans > 9,9-epoxylignans > Dibenzylbutyrolactone lignans
IUPAC Name (3E,4S)-4-(1,3-benzodioxol-5-ylmethyl)-3-(1,3-benzodioxol-5-ylmethylidene)-4-hydroxyoxolan-2-one
SMILES (Canonical) C1C(C(=CC2=CC3=C(C=C2)OCO3)C(=O)O1)(CC4=CC5=C(C=C4)OCO5)O
SMILES (Isomeric) C1[C@@](/C(=C\C2=CC3=C(C=C2)OCO3)/C(=O)O1)(CC4=CC5=C(C=C4)OCO5)O
InChI InChI=1S/C20H16O7/c21-19-14(5-12-1-3-15-17(6-12)26-10-24-15)20(22,9-23-19)8-13-2-4-16-18(7-13)27-11-25-16/h1-7,22H,8-11H2/b14-5-/t20-/m1/s1
InChI Key BWMJBJJDRXPGGP-UCJKYMQBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H16O7
Molecular Weight 368.30 g/mol
Exact Mass 368.08960285 g/mol
Topological Polar Surface Area (TPSA) 83.40 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3E,4S)-4-(1,3-benzodioxol-5-ylmethyl)-3-(1,3-benzodioxol-5-ylmethylidene)-4-hydroxyoxolan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.5936 59.36%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7464 74.64%
OATP2B1 inhibitior - 0.8623 86.23%
OATP1B1 inhibitior + 0.9410 94.10%
OATP1B3 inhibitior + 0.9495 94.95%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.9289 92.89%
P-glycoprotein inhibitior + 0.7230 72.30%
P-glycoprotein substrate - 0.9243 92.43%
CYP3A4 substrate - 0.5324 53.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8355 83.55%
CYP3A4 inhibition + 0.5292 52.92%
CYP2C9 inhibition - 0.6242 62.42%
CYP2C19 inhibition + 0.5123 51.23%
CYP2D6 inhibition - 0.5631 56.31%
CYP1A2 inhibition - 0.6428 64.28%
CYP2C8 inhibition - 0.8319 83.19%
CYP inhibitory promiscuity + 0.5438 54.38%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.3921 39.21%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.5055 50.55%
Skin irritation - 0.6904 69.04%
Skin corrosion - 0.9368 93.68%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6024 60.24%
Micronuclear + 0.7333 73.33%
Hepatotoxicity + 0.6324 63.24%
skin sensitisation - 0.5577 55.77%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.4748 47.48%
Acute Oral Toxicity (c) III 0.4803 48.03%
Estrogen receptor binding + 0.8865 88.65%
Androgen receptor binding + 0.8436 84.36%
Thyroid receptor binding + 0.6179 61.79%
Glucocorticoid receptor binding + 0.5524 55.24%
Aromatase binding + 0.5664 56.64%
PPAR gamma + 0.8262 82.62%
Honey bee toxicity - 0.8263 82.63%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9639 96.39%

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 98.24% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.88% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.70% 94.45%
CHEMBL2581 P07339 Cathepsin D 96.04% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.51% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.36% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 91.87% 94.80%
CHEMBL2039 P27338 Monoamine oxidase B 90.84% 92.51%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.43% 89.00%
CHEMBL230 P35354 Cyclooxygenase-2 84.84% 89.63%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.97% 92.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.75% 96.00%

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.
Taiwania cryptomerioides

Cross-Links

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PubChem 163190838
LOTUS LTS0097649
wikiData Q103788389