7-methoxy-9H-carbazole-3-carbaldehyde

Details

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Internal ID 99f77f0b-6275-4a5a-9c23-268fc77cebc1
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 7-methoxy-9H-carbazole-3-carbaldehyde
SMILES (Canonical) COC1=CC2=C(C=C1)C3=C(N2)C=CC(=C3)C=O
SMILES (Isomeric) COC1=CC2=C(C=C1)C3=C(N2)C=CC(=C3)C=O
InChI InChI=1S/C14H11NO2/c1-17-10-3-4-11-12-6-9(8-16)2-5-13(12)15-14(11)7-10/h2-8,15H,1H3
InChI Key IBDBRUPJUXYODT-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C14H11NO2
Molecular Weight 225.24 g/mol
Exact Mass 225.078978594 g/mol
Topological Polar Surface Area (TPSA) 42.10 Ų
XlogP 2.80

Synonyms

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Clauszoline-K
7-methoxy-9H-carbazole-3-carbaldehyde
CHEMBL1927326

2D Structure

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2D Structure of 7-methoxy-9H-carbazole-3-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

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
CHEMBL1951 P21397 Monoamine oxidase A 98.55% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.75% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.34% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.91% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.89% 96.09%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 90.67% 93.24%
CHEMBL2535 P11166 Glucose transporter 87.25% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.07% 96.00%
CHEMBL4208 P20618 Proteasome component C5 86.93% 90.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 86.48% 91.71%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.08% 86.92%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.14% 85.30%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 82.64% 96.47%
CHEMBL1907 P15144 Aminopeptidase N 81.76% 93.31%

Cross-Links

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PubChem 10537169
NPASS NPC249583
ChEMBL CHEMBL1927326
LOTUS LTS0189900
wikiData Q105036434