(2S)-6-acetyl-8-methoxy-2-prop-1-en-2-yl-1,3-benzodioxin-4-one

Details

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Internal ID ed6d1b01-2972-4c5e-9f76-a86c3e13e402
Taxonomy Organoheterocyclic compounds > Benzodioxanes > Benzo-1,3-dioxanes
IUPAC Name (2S)-6-acetyl-8-methoxy-2-prop-1-en-2-yl-1,3-benzodioxin-4-one
SMILES (Canonical) CC(=C)C1OC2=C(C=C(C=C2OC)C(=O)C)C(=O)O1
SMILES (Isomeric) CC(=C)[C@H]1OC2=C(C=C(C=C2OC)C(=O)C)C(=O)O1
InChI InChI=1S/C14H14O5/c1-7(2)14-18-12-10(13(16)19-14)5-9(8(3)15)6-11(12)17-4/h5-6,14H,1H2,2-4H3/t14-/m0/s1
InChI Key MXKGVFUUQQSGIG-AWEZNQCLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14O5
Molecular Weight 262.26 g/mol
Exact Mass 262.08412354 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.35
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-6-acetyl-8-methoxy-2-prop-1-en-2-yl-1,3-benzodioxin-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9845 98.45%
Caco-2 + 0.6369 63.69%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6136 61.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9205 92.05%
OATP1B3 inhibitior + 0.9447 94.47%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7171 71.71%
P-glycoprotein inhibitior - 0.7445 74.45%
P-glycoprotein substrate - 0.7629 76.29%
CYP3A4 substrate + 0.5302 53.02%
CYP2C9 substrate - 0.5898 58.98%
CYP2D6 substrate - 0.8479 84.79%
CYP3A4 inhibition + 0.7223 72.23%
CYP2C9 inhibition - 0.9037 90.37%
CYP2C19 inhibition + 0.6470 64.70%
CYP2D6 inhibition - 0.8870 88.70%
CYP1A2 inhibition + 0.6014 60.14%
CYP2C8 inhibition - 0.7823 78.23%
CYP inhibitory promiscuity + 0.6697 66.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9718 97.18%
Carcinogenicity (trinary) Non-required 0.5348 53.48%
Eye corrosion - 0.9596 95.96%
Eye irritation + 0.6225 62.25%
Skin irritation - 0.7255 72.55%
Skin corrosion - 0.9702 97.02%
Ames mutagenesis - 0.6954 69.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5187 51.87%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.7058 70.58%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5432 54.32%
Acute Oral Toxicity (c) II 0.6363 63.63%
Estrogen receptor binding + 0.5632 56.32%
Androgen receptor binding - 0.6819 68.19%
Thyroid receptor binding + 0.5387 53.87%
Glucocorticoid receptor binding - 0.5809 58.09%
Aromatase binding + 0.5266 52.66%
PPAR gamma - 0.5184 51.84%
Honey bee toxicity - 0.7918 79.18%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5049 50.49%
Fish aquatic toxicity + 0.9764 97.64%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.53% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.51% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.36% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.43% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 87.59% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.11% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.40% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.90% 85.14%
CHEMBL2535 P11166 Glucose transporter 85.84% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.59% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.42% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.26% 97.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.71% 96.95%
CHEMBL2581 P07339 Cathepsin D 81.70% 98.95%

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.
Ligularia macrophylla
Ligularia veitchiana

Cross-Links

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PubChem 162976304
LOTUS LTS0120195
wikiData Q105174248