5,6,7-Trimethoxy-2-propan-2-ylidene-1,4-benzodioxin-3-one

Details

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Internal ID 97892acf-65fd-4e8b-bfe2-72fab5f2b4ea
Taxonomy Organoheterocyclic compounds > Benzodioxanes > Benzo-1,4-dioxanes
IUPAC Name 5,6,7-trimethoxy-2-propan-2-ylidene-1,4-benzodioxin-3-one
SMILES (Canonical) CC(=C1C(=O)OC2=C(C(=C(C=C2O1)OC)OC)OC)C
SMILES (Isomeric) CC(=C1C(=O)OC2=C(C(=C(C=C2O1)OC)OC)OC)C
InChI InChI=1S/C14H16O6/c1-7(2)10-14(15)20-12-9(19-10)6-8(16-3)11(17-4)13(12)18-5/h6H,1-5H3
InChI Key AHFPJUFRLQTVDU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16O6
Molecular Weight 280.27 g/mol
Exact Mass 280.09468823 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.30
H-Bond Acceptor 6
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 5,6,7-Trimethoxy-2-propan-2-ylidene-1,4-benzodioxin-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.8610 86.10%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6599 65.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9455 94.55%
OATP1B3 inhibitior + 0.9691 96.91%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6645 66.45%
P-glycoprotein inhibitior - 0.8261 82.61%
P-glycoprotein substrate - 0.9597 95.97%
CYP3A4 substrate - 0.5710 57.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8530 85.30%
CYP3A4 inhibition + 0.5936 59.36%
CYP2C9 inhibition - 0.8241 82.41%
CYP2C19 inhibition + 0.9071 90.71%
CYP2D6 inhibition - 0.7637 76.37%
CYP1A2 inhibition + 0.7512 75.12%
CYP2C8 inhibition - 0.7370 73.70%
CYP inhibitory promiscuity + 0.8566 85.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9718 97.18%
Carcinogenicity (trinary) Danger 0.4752 47.52%
Eye corrosion - 0.9698 96.98%
Eye irritation + 0.9355 93.55%
Skin irritation - 0.7236 72.36%
Skin corrosion - 0.9799 97.99%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6087 60.87%
Micronuclear + 0.6400 64.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.7670 76.70%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5070 50.70%
Acute Oral Toxicity (c) III 0.4755 47.55%
Estrogen receptor binding + 0.7061 70.61%
Androgen receptor binding - 0.6646 66.46%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.5893 58.93%
Aromatase binding + 0.5430 54.30%
PPAR gamma - 0.5342 53.42%
Honey bee toxicity - 0.8684 86.84%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5449 54.49%
Fish aquatic toxicity + 0.9719 97.19%

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 95.30% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.28% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.07% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.37% 94.00%
CHEMBL2581 P07339 Cathepsin D 88.52% 98.95%
CHEMBL2535 P11166 Glucose transporter 86.92% 98.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.14% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 85.22% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.83% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.62% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.10% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.91% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.52% 99.23%

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.
Calea prunifolia

Cross-Links

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PubChem 162892598
LOTUS LTS0246561
wikiData Q104912221