2-(1-methoxy-3-methyl-9H-carbazol-4-yl)-3-methyl-9H-carbazole-1,4-dione

Details

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Internal ID 18ed3fde-9466-4eb9-8faf-b41070bdf7a9
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 2-(1-methoxy-3-methyl-9H-carbazol-4-yl)-3-methyl-9H-carbazole-1,4-dione
SMILES (Canonical) CC1=CC(=C2C(=C1C3=C(C(=O)C4=C(C3=O)NC5=CC=CC=C54)C)C6=CC=CC=C6N2)OC
SMILES (Isomeric) CC1=CC(=C2C(=C1C3=C(C(=O)C4=C(C3=O)NC5=CC=CC=C54)C)C6=CC=CC=C6N2)OC
InChI InChI=1S/C27H20N2O3/c1-13-12-19(32-3)24-22(15-8-4-6-10-17(15)28-24)20(13)21-14(2)26(30)23-16-9-5-7-11-18(16)29-25(23)27(21)31/h4-12,28-29H,1-3H3
InChI Key WNIJCVSAQYOBMV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H20N2O3
Molecular Weight 420.50 g/mol
Exact Mass 420.14739250 g/mol
Topological Polar Surface Area (TPSA) 75.00 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.97
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(1-methoxy-3-methyl-9H-carbazol-4-yl)-3-methyl-9H-carbazole-1,4-dione

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 + 0.6288 62.88%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8810 88.10%
OATP2B1 inhibitior - 0.7171 71.71%
OATP1B1 inhibitior + 0.8881 88.81%
OATP1B3 inhibitior + 0.9357 93.57%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9322 93.22%
P-glycoprotein inhibitior + 0.8545 85.45%
P-glycoprotein substrate - 0.8175 81.75%
CYP3A4 substrate + 0.5998 59.98%
CYP2C9 substrate + 0.5886 58.86%
CYP2D6 substrate - 0.8365 83.65%
CYP3A4 inhibition + 0.8688 86.88%
CYP2C9 inhibition + 0.9192 91.92%
CYP2C19 inhibition + 0.8595 85.95%
CYP2D6 inhibition - 0.8130 81.30%
CYP1A2 inhibition + 0.8672 86.72%
CYP2C8 inhibition + 0.7478 74.78%
CYP inhibitory promiscuity + 0.9648 96.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9143 91.43%
Carcinogenicity (trinary) Non-required 0.3868 38.68%
Eye corrosion - 0.9937 99.37%
Eye irritation - 0.7953 79.53%
Skin irritation - 0.8883 88.83%
Skin corrosion - 0.9507 95.07%
Ames mutagenesis + 0.7936 79.36%
Human Ether-a-go-go-Related Gene inhibition + 0.7676 76.76%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.5876 58.76%
skin sensitisation - 0.9128 91.28%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.6243 62.43%
Acute Oral Toxicity (c) III 0.6238 62.38%
Estrogen receptor binding + 0.9466 94.66%
Androgen receptor binding + 0.7775 77.75%
Thyroid receptor binding + 0.7078 70.78%
Glucocorticoid receptor binding + 0.7713 77.13%
Aromatase binding - 0.5350 53.50%
PPAR gamma + 0.7907 79.07%
Honey bee toxicity - 0.8249 82.49%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9529 95.29%

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 98.51% 95.56%
CHEMBL4302 P08183 P-glycoprotein 1 97.07% 92.98%
CHEMBL3192 Q9BY41 Histone deacetylase 8 96.09% 93.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.78% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.53% 98.95%
CHEMBL240 Q12809 HERG 94.25% 89.76%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.92% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.04% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.91% 89.00%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 89.44% 92.67%
CHEMBL1951 P21397 Monoamine oxidase A 89.23% 91.49%
CHEMBL2535 P11166 Glucose transporter 88.40% 98.75%
CHEMBL1907 P15144 Aminopeptidase N 87.93% 93.31%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 87.59% 81.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.70% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.36% 96.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 86.28% 96.67%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 86.01% 85.49%
CHEMBL3524 P56524 Histone deacetylase 4 85.80% 92.97%
CHEMBL3401 O75469 Pregnane X receptor 84.65% 94.73%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 84.61% 85.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.30% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.97% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.15% 85.14%
CHEMBL1795185 Q58F21 Bromodomain testis-specific protein 82.43% 89.76%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 81.87% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.11% 96.09%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 81.04% 98.21%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.95% 96.21%

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 10432264
LOTUS LTS0096834
wikiData Q105309101