1-methoxy-9-(1-methoxy-9H-carbazol-3-yl)-3-methylcarbazole

Details

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Internal ID a3f0cdc5-e13c-4dd4-85cc-ea27e0083858
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 1-methoxy-9-(1-methoxy-9H-carbazol-3-yl)-3-methylcarbazole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H22N2O2/c1-16-12-21-19-9-5-7-11-23(19)29(27(21)25(13-16)31-3)17-14-20-18-8-4-6-10-22(18)28-26(20)24(15-17)30-2/h4-15,28H,1-3H3
InChI Key YMKKERLGXGTYBK-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C27H22N2O2
Molecular Weight 406.50 g/mol
Exact Mass 406.168127949 g/mol
Topological Polar Surface Area (TPSA) 39.20 Ų
XlogP 6.80
Atomic LogP (AlogP) 6.74
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-methoxy-9-(1-methoxy-9H-carbazol-3-yl)-3-methylcarbazole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9893 98.93%
Caco-2 + 0.7143 71.43%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7881 78.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8657 86.57%
OATP1B3 inhibitior + 0.9380 93.80%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7598 75.98%
BSEP inhibitior + 0.9720 97.20%
P-glycoprotein inhibitior + 0.8714 87.14%
P-glycoprotein substrate - 0.5124 51.24%
CYP3A4 substrate + 0.6097 60.97%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.6897 68.97%
CYP3A4 inhibition + 0.8422 84.22%
CYP2C9 inhibition + 0.7477 74.77%
CYP2C19 inhibition + 0.8895 88.95%
CYP2D6 inhibition + 0.6541 65.41%
CYP1A2 inhibition + 0.9284 92.84%
CYP2C8 inhibition + 0.7795 77.95%
CYP inhibitory promiscuity + 0.9279 92.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9008 90.08%
Carcinogenicity (trinary) Warning 0.3909 39.09%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.6093 60.93%
Skin irritation - 0.8324 83.24%
Skin corrosion - 0.9347 93.47%
Ames mutagenesis + 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8181 81.81%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.9345 93.45%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.8254 82.54%
Acute Oral Toxicity (c) III 0.6577 65.77%
Estrogen receptor binding + 0.9511 95.11%
Androgen receptor binding + 0.7873 78.73%
Thyroid receptor binding + 0.8425 84.25%
Glucocorticoid receptor binding + 0.8577 85.77%
Aromatase binding + 0.6343 63.43%
PPAR gamma + 0.6930 69.30%
Honey bee toxicity - 0.8888 88.88%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity + 0.7700 77.00%
Fish aquatic toxicity - 0.3744 37.44%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.04% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.38% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.89% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.26% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 90.25% 91.49%
CHEMBL2535 P11166 Glucose transporter 89.87% 98.75%
CHEMBL4302 P08183 P-glycoprotein 1 89.37% 92.98%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.01% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.47% 93.99%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 84.13% 97.31%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.05% 96.00%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 83.73% 98.21%
CHEMBL255 P29275 Adenosine A2b receptor 83.13% 98.59%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.81% 91.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.52% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.30% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.69% 94.45%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 81.10% 85.49%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.72% 89.62%
CHEMBL1781 P11387 DNA topoisomerase I 80.54% 97.00%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 80.51% 100.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.50% 97.21%

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.
Bergera euchrestifolia

Cross-Links

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PubChem 14634645
LOTUS LTS0140045
wikiData Q105350577