Dielsiquinone

Details

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Internal ID 978afaec-0824-498b-b1b3-70f689059dca
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines
IUPAC Name 3-methoxy-4-methyl-1H-benzo[g]quinoline-2,5,10-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H11NO4/c1-7-10-11(16-15(19)14(7)20-2)13(18)9-6-4-3-5-8(9)12(10)17/h3-6H,1-2H3,(H,16,19)
InChI Key AZTABGJRYQJTCL-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C15H11NO4
Molecular Weight 269.25 g/mol
Exact Mass 269.06880783 g/mol
Topological Polar Surface Area (TPSA) 72.50 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.47
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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3-methoxy-4-methyl-1H-benzo(g)quinoline-2,5,10-trione
3-methoxy-4-methyl-1H-benzo[g]quinoline-2,5,10-trione
RefChem:133329
104696-15-3
CHEMBL479282
SCHEMBL31237174

2D Structure

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2D Structure of Dielsiquinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9847 98.47%
Caco-2 + 0.5448 54.48%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.6952 69.52%
OATP2B1 inhibitior - 0.8637 86.37%
OATP1B1 inhibitior + 0.9267 92.67%
OATP1B3 inhibitior + 0.9707 97.07%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5626 56.26%
P-glycoprotein inhibitior - 0.7567 75.67%
P-glycoprotein substrate - 0.9384 93.84%
CYP3A4 substrate - 0.5480 54.80%
CYP2C9 substrate + 0.6277 62.77%
CYP2D6 substrate - 0.8745 87.45%
CYP3A4 inhibition - 0.6293 62.93%
CYP2C9 inhibition - 0.7706 77.06%
CYP2C19 inhibition - 0.8695 86.95%
CYP2D6 inhibition - 0.9496 94.96%
CYP1A2 inhibition + 0.8322 83.22%
CYP2C8 inhibition - 0.8819 88.19%
CYP inhibitory promiscuity - 0.5233 52.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6184 61.84%
Eye corrosion - 0.9933 99.33%
Eye irritation - 0.6379 63.79%
Skin irritation - 0.8670 86.70%
Skin corrosion - 0.9771 97.71%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7132 71.32%
Micronuclear + 0.7759 77.59%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.9563 95.63%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6668 66.68%
Acute Oral Toxicity (c) III 0.6507 65.07%
Estrogen receptor binding + 0.5931 59.31%
Androgen receptor binding + 0.6643 66.43%
Thyroid receptor binding - 0.5209 52.09%
Glucocorticoid receptor binding + 0.7120 71.20%
Aromatase binding + 0.7331 73.31%
PPAR gamma - 0.6836 68.36%
Honey bee toxicity - 0.8628 86.28%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.5199 51.99%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.07% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.54% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.84% 99.23%
CHEMBL2535 P11166 Glucose transporter 91.17% 98.75%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.87% 93.03%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.37% 82.69%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.05% 96.67%
CHEMBL1937 Q92769 Histone deacetylase 2 82.98% 94.75%
CHEMBL3401 O75469 Pregnane X receptor 81.66% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.38% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.49% 91.11%

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.
Goniothalamus tamirensis
Guatteria blepharophylla

Cross-Links

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PubChem 10445779
LOTUS LTS0108277
wikiData Q104921912