Carbazoquinocin E

Details

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Internal ID 91b258e9-d8c2-4eb9-acda-97f50a407a6e
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 2-methyl-1-(6-methylheptyl)-9H-carbazole-3,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H25NO2/c1-13(2)9-5-4-6-10-15-14(3)20(23)21(24)18-16-11-7-8-12-17(16)22-19(15)18/h7-8,11-13,22H,4-6,9-10H2,1-3H3
InChI Key DFUKYENOHDYPTJ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C21H25NO2
Molecular Weight 323.40 g/mol
Exact Mass 323.188529040 g/mol
Topological Polar Surface Area (TPSA) 49.90 Ų
XlogP 5.30
Atomic LogP (AlogP) 5.31
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Carbazoquinocin E

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 + 0.6170 61.70%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7361 73.61%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.9166 91.66%
OATP1B3 inhibitior + 0.9217 92.17%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.8899 88.99%
P-glycoprotein inhibitior - 0.5713 57.13%
P-glycoprotein substrate - 0.6385 63.85%
CYP3A4 substrate + 0.6210 62.10%
CYP2C9 substrate - 0.5809 58.09%
CYP2D6 substrate - 0.8327 83.27%
CYP3A4 inhibition + 0.6865 68.65%
CYP2C9 inhibition + 0.6817 68.17%
CYP2C19 inhibition + 0.8181 81.81%
CYP2D6 inhibition - 0.6982 69.82%
CYP1A2 inhibition + 0.9268 92.68%
CYP2C8 inhibition - 0.7708 77.08%
CYP inhibitory promiscuity + 0.9343 93.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5792 57.92%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.8828 88.28%
Skin irritation - 0.7747 77.47%
Skin corrosion - 0.9306 93.06%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8287 82.87%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.5033 50.33%
skin sensitisation - 0.7679 76.79%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6073 60.73%
Acute Oral Toxicity (c) III 0.6037 60.37%
Estrogen receptor binding + 0.6513 65.13%
Androgen receptor binding + 0.7781 77.81%
Thyroid receptor binding + 0.5912 59.12%
Glucocorticoid receptor binding + 0.7627 76.27%
Aromatase binding + 0.5740 57.40%
PPAR gamma + 0.6981 69.81%
Honey bee toxicity - 0.9344 93.44%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9959 99.59%

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 98.75% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.50% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 95.41% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.76% 94.45%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 94.00% 85.94%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.75% 93.99%
CHEMBL1907 P15144 Aminopeptidase N 92.70% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 92.52% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.21% 91.11%
CHEMBL5103 Q969S8 Histone deacetylase 10 92.21% 90.08%
CHEMBL3310 Q96DB2 Histone deacetylase 11 92.06% 88.56%
CHEMBL2885 P07451 Carbonic anhydrase III 91.10% 87.45%
CHEMBL3524 P56524 Histone deacetylase 4 90.50% 92.97%
CHEMBL255 P29275 Adenosine A2b receptor 89.94% 98.59%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.57% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.07% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.95% 96.09%
CHEMBL1829 O15379 Histone deacetylase 3 85.89% 95.00%
CHEMBL240 Q12809 HERG 85.73% 89.76%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.54% 94.80%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.49% 96.47%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.12% 93.56%
CHEMBL4302 P08183 P-glycoprotein 1 82.65% 92.98%
CHEMBL1781 P11387 DNA topoisomerase I 82.15% 97.00%
CHEMBL2179 P04062 Beta-glucocerebrosidase 81.87% 85.31%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 81.44% 83.10%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.15% 94.62%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.27% 91.71%
CHEMBL2535 P11166 Glucose transporter 80.15% 98.75%

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 10381539
LOTUS LTS0172546
wikiData Q77494743