Methyl 5-hydroxy-2-methylidene-3-oxo-4a,5,8,8a-tetrahydro-1,4-benzodioxine-7-carboxylate

Details

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Internal ID 5a619b74-81dc-43f5-b7ee-2940abef39d0
Taxonomy Organoheterocyclic compounds > Dioxanes > 1,4-dioxanes
IUPAC Name methyl 5-hydroxy-2-methylidene-3-oxo-4a,5,8,8a-tetrahydro-1,4-benzodioxine-7-carboxylate
SMILES (Canonical) COC(=O)C1=CC(C2C(C1)OC(=C)C(=O)O2)O
SMILES (Isomeric) COC(=O)C1=CC(C2C(C1)OC(=C)C(=O)O2)O
InChI InChI=1S/C11H12O6/c1-5-10(13)17-9-7(12)3-6(11(14)15-2)4-8(9)16-5/h3,7-9,12H,1,4H2,2H3
InChI Key WTZRTZIWWAIJQP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O6
Molecular Weight 240.21 g/mol
Exact Mass 240.06338810 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 0.40
Atomic LogP (AlogP) -0.33
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 5-hydroxy-2-methylidene-3-oxo-4a,5,8,8a-tetrahydro-1,4-benzodioxine-7-carboxylate

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 - 0.6556 65.56%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7037 70.37%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8862 88.62%
OATP1B3 inhibitior + 0.9633 96.33%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9665 96.65%
P-glycoprotein inhibitior - 0.9389 93.89%
P-glycoprotein substrate - 0.8756 87.56%
CYP3A4 substrate + 0.5555 55.55%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8487 84.87%
CYP3A4 inhibition - 0.5926 59.26%
CYP2C9 inhibition - 0.8445 84.45%
CYP2C19 inhibition - 0.8017 80.17%
CYP2D6 inhibition - 0.9189 91.89%
CYP1A2 inhibition - 0.7986 79.86%
CYP2C8 inhibition - 0.8398 83.98%
CYP inhibitory promiscuity - 0.8106 81.06%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Danger 0.4416 44.16%
Eye corrosion - 0.9683 96.83%
Eye irritation - 0.4789 47.89%
Skin irritation - 0.6409 64.09%
Skin corrosion - 0.9229 92.29%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6958 69.58%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.7493 74.93%
skin sensitisation - 0.7877 78.77%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.6940 69.40%
Acute Oral Toxicity (c) III 0.3801 38.01%
Estrogen receptor binding - 0.6794 67.94%
Androgen receptor binding - 0.7638 76.38%
Thyroid receptor binding - 0.7220 72.20%
Glucocorticoid receptor binding - 0.6927 69.27%
Aromatase binding - 0.7802 78.02%
PPAR gamma - 0.6360 63.60%
Honey bee toxicity - 0.8317 83.17%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6611 66.11%
Fish aquatic toxicity + 0.7817 78.17%

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 95.43% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.29% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.86% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.93% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.66% 86.33%
CHEMBL5028 O14672 ADAM10 80.32% 97.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163057928
LOTUS LTS0162173
wikiData Q105312887