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

Details

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Internal ID cc0ec1be-81f6-40e8-8678-cc15f3e6c6ea
Taxonomy Lignans, neolignans and related compounds > Furanoid lignans > Tetrahydrofuran lignans > 9,9-epoxylignans > Dibenzylbutyrolactone lignans
IUPAC Name 4-(1,3-benzodioxol-5-ylmethyl)-3-(1,3-benzodioxol-5-ylmethylidene)-5-hydroxyoxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H16O7/c21-19-13(5-11-1-3-15-17(7-11)25-9-23-15)14(20(22)27-19)6-12-2-4-16-18(8-12)26-10-24-16/h1-5,7-8,14,20,22H,6,9-10H2
InChI Key OFNLHWUUBXCFIC-UHFFFAOYSA-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) 83.50 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.26
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 4-(1,3-Benzodioxol-5-ylmethyl)-3-(1,3-benzodioxol-5-ylmethylidene)-5-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 + 0.9925 99.25%
Caco-2 - 0.5681 56.81%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7766 77.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9200 92.00%
OATP1B3 inhibitior + 0.9569 95.69%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9047 90.47%
P-glycoprotein inhibitior + 0.6868 68.68%
P-glycoprotein substrate - 0.9200 92.00%
CYP3A4 substrate - 0.5280 52.80%
CYP2C9 substrate - 0.6060 60.60%
CYP2D6 substrate - 0.8410 84.10%
CYP3A4 inhibition + 0.6281 62.81%
CYP2C9 inhibition + 0.7119 71.19%
CYP2C19 inhibition + 0.7339 73.39%
CYP2D6 inhibition - 0.6201 62.01%
CYP1A2 inhibition + 0.6005 60.05%
CYP2C8 inhibition - 0.8315 83.15%
CYP inhibitory promiscuity + 0.7720 77.20%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4921 49.21%
Eye corrosion - 0.9852 98.52%
Eye irritation - 0.7441 74.41%
Skin irritation - 0.6434 64.34%
Skin corrosion - 0.9435 94.35%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4000 40.00%
Micronuclear + 0.7874 78.74%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.5451 54.51%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7521 75.21%
Acute Oral Toxicity (c) III 0.4268 42.68%
Estrogen receptor binding + 0.8378 83.78%
Androgen receptor binding + 0.6197 61.97%
Thyroid receptor binding + 0.5333 53.33%
Glucocorticoid receptor binding - 0.5087 50.87%
Aromatase binding - 0.5829 58.29%
PPAR gamma + 0.8379 83.79%
Honey bee toxicity - 0.8335 83.35%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9890 98.90%

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 97.73% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.14% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.08% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 95.98% 94.80%
CHEMBL2581 P07339 Cathepsin D 92.91% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 91.48% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.72% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.63% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.92% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.30% 86.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.75% 93.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.44% 93.40%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 84.15% 83.57%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.84% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 83.39% 94.73%
CHEMBL1929 P47989 Xanthine dehydrogenase 82.90% 96.12%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.97% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.50% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.09% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.01% 96.09%

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.
Calocedrus formosana
Pterocarpus santalinus

Cross-Links

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PubChem 85087885
LOTUS LTS0223411
wikiData Q105191290