Koeniginequinone A

Details

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Internal ID 212a6898-62fb-472d-a069-59694333215b
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 7-methoxy-3-methyl-9H-carbazole-1,4-dione
SMILES (Canonical) CC1=CC(=O)C2=C(C1=O)C3=C(N2)C=C(C=C3)OC
SMILES (Isomeric) CC1=CC(=O)C2=C(C1=O)C3=C(N2)C=C(C=C3)OC
InChI InChI=1S/C14H11NO3/c1-7-5-11(16)13-12(14(7)17)9-4-3-8(18-2)6-10(9)15-13/h3-6,15H,1-2H3
InChI Key FBXPHUZRLGTRFW-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C14H11NO3
Molecular Weight 241.24 g/mol
Exact Mass 241.07389321 g/mol
Topological Polar Surface Area (TPSA) 59.20 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.50
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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110519-58-9
7-methoxy-3-methyl-9H-carbazole-1,4-dione
1H-Carbazole-1,4(9H)-dione, 7-methoxy-3-methyl-
CHEMBL496241
DTXSID30460552
CHEBI:173738
7-Methoxy-3-methyl-1,4-carbazolequinone
7-Methoxy-3-methyl-1H-carbazole-1,4(9H)-dione
7-METHOXY-3-METHYL-4,9-DIHYDRO-1H-CARBAZOLE-1,4-DIONE

2D Structure

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2D Structure of Koeniginequinone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7998 79.98%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9214 92.14%
OATP1B3 inhibitior + 0.9630 96.30%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5828 58.28%
P-glycoprotein inhibitior - 0.9383 93.83%
P-glycoprotein substrate - 0.8985 89.85%
CYP3A4 substrate + 0.5542 55.42%
CYP2C9 substrate + 0.6110 61.10%
CYP2D6 substrate - 0.8564 85.64%
CYP3A4 inhibition + 0.7217 72.17%
CYP2C9 inhibition + 0.8383 83.83%
CYP2C19 inhibition + 0.7096 70.96%
CYP2D6 inhibition - 0.8128 81.28%
CYP1A2 inhibition + 0.9652 96.52%
CYP2C8 inhibition - 0.7412 74.12%
CYP inhibitory promiscuity + 0.9560 95.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8753 87.53%
Carcinogenicity (trinary) Non-required 0.4583 45.83%
Eye corrosion - 0.9932 99.32%
Eye irritation + 0.5741 57.41%
Skin irritation - 0.8801 88.01%
Skin corrosion - 0.9683 96.83%
Ames mutagenesis + 0.6463 64.63%
Human Ether-a-go-go-Related Gene inhibition - 0.4286 42.86%
Micronuclear + 0.8259 82.59%
Hepatotoxicity + 0.5585 55.85%
skin sensitisation - 0.8908 89.08%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6792 67.92%
Acute Oral Toxicity (c) III 0.6428 64.28%
Estrogen receptor binding + 0.7732 77.32%
Androgen receptor binding + 0.8530 85.30%
Thyroid receptor binding + 0.5548 55.48%
Glucocorticoid receptor binding + 0.7802 78.02%
Aromatase binding + 0.7632 76.32%
PPAR gamma - 0.5484 54.84%
Honey bee toxicity - 0.8811 88.11%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9451 94.51%

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 98.22% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.92% 94.45%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.92% 93.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.41% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.04% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.88% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 89.70% 94.75%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 89.66% 85.30%
CHEMBL1907 P15144 Aminopeptidase N 89.45% 93.31%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.68% 86.92%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.27% 94.80%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 86.99% 96.67%
CHEMBL2535 P11166 Glucose transporter 86.71% 98.75%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 86.64% 96.47%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 86.19% 93.24%
CHEMBL4208 P20618 Proteasome component C5 84.74% 90.00%
CHEMBL1951 P21397 Monoamine oxidase A 84.10% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.27% 99.23%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 83.23% 85.49%
CHEMBL255 P29275 Adenosine A2b receptor 83.18% 98.59%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 82.92% 92.67%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.42% 99.15%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.58% 91.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.54% 96.09%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 81.17% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.05% 96.00%

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.
Murraya koenigii

Cross-Links

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PubChem 11264975
LOTUS LTS0067002
wikiData Q82284626