Dimethyl azulene-1,4-dicarboxylate

Details

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Internal ID 9362aa75-4adb-4bd6-b2a6-3f89f1abadcd
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Cyclic olefins > Azulenes
IUPAC Name dimethyl azulene-1,4-dicarboxylate
SMILES (Canonical) COC(=O)C1=CC=CC=C2C1=CC=C2C(=O)OC
SMILES (Isomeric) COC(=O)C1=CC=CC=C2C1=CC=C2C(=O)OC
InChI InChI=1S/C14H12O4/c1-17-13(15)11-6-4-3-5-9-10(11)7-8-12(9)14(16)18-2/h3-8H,1-2H3
InChI Key SJKWHMYKQXMFMI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H12O4
Molecular Weight 244.24 g/mol
Exact Mass 244.07355886 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dimethyl azulene-1,4-dicarboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9878 98.78%
Caco-2 + 0.8192 81.92%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Mitochondria 0.5436 54.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9405 94.05%
OATP1B3 inhibitior + 0.9620 96.20%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6072 60.72%
P-glycoprotein inhibitior - 0.8392 83.92%
P-glycoprotein substrate - 0.9351 93.51%
CYP3A4 substrate - 0.6101 61.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7932 79.32%
CYP3A4 inhibition - 0.9330 93.30%
CYP2C9 inhibition - 0.8771 87.71%
CYP2C19 inhibition - 0.9066 90.66%
CYP2D6 inhibition - 0.9322 93.22%
CYP1A2 inhibition + 0.5794 57.94%
CYP2C8 inhibition - 0.7337 73.37%
CYP inhibitory promiscuity - 0.9315 93.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6774 67.74%
Carcinogenicity (trinary) Non-required 0.6889 68.89%
Eye corrosion - 0.6045 60.45%
Eye irritation + 0.9397 93.97%
Skin irritation - 0.7558 75.58%
Skin corrosion - 0.8978 89.78%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6471 64.71%
Micronuclear - 0.7341 73.41%
Hepatotoxicity - 0.5289 52.89%
skin sensitisation - 0.5466 54.66%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.7945 79.45%
Acute Oral Toxicity (c) III 0.5178 51.78%
Estrogen receptor binding + 0.9047 90.47%
Androgen receptor binding + 0.5789 57.89%
Thyroid receptor binding - 0.6440 64.40%
Glucocorticoid receptor binding - 0.5064 50.64%
Aromatase binding + 0.7167 71.67%
PPAR gamma - 0.7975 79.75%
Honey bee toxicity - 0.9659 96.59%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9449 94.49%

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
CHEMBL2581 P07339 Cathepsin D 95.88% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.12% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.91% 91.11%
CHEMBL2535 P11166 Glucose transporter 87.26% 98.75%
CHEMBL4208 P20618 Proteasome component C5 85.31% 90.00%
CHEMBL221 P23219 Cyclooxygenase-1 83.95% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.34% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.28% 95.50%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.19% 96.67%
CHEMBL3401 O75469 Pregnane X receptor 81.68% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.62% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 80.59% 91.49%
CHEMBL5028 O14672 ADAM10 80.30% 97.50%

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.
Helichrysum ambiguum

Cross-Links

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PubChem 14262772
LOTUS LTS0004856
wikiData Q105254385