N-methoxy-3-formylcarbazole

Details

Top
Internal ID 18769cf1-49b1-4032-a4d8-abea7b51e06a
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 9-methoxycarbazole-3-carbaldehyde
SMILES (Canonical) CON1C2=C(C=C(C=C2)C=O)C3=CC=CC=C31
SMILES (Isomeric) CON1C2=C(C=C(C=C2)C=O)C3=CC=CC=C31
InChI InChI=1S/C14H11NO2/c1-17-15-13-5-3-2-4-11(13)12-8-10(9-16)6-7-14(12)15/h2-9H,1H3
InChI Key LGLGSEILIYMFIQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H11NO2
Molecular Weight 225.24 g/mol
Exact Mass 225.078978594 g/mol
Topological Polar Surface Area (TPSA) 31.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
117592-01-5
9-Methoxy-9H-carbazole-3-carbaldehyde
AKOS040763262
F92925

2D Structure

Top
2D Structure of N-methoxy-3-formylcarbazole

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8598 85.98%
Blood Brain Barrier + 0.8817 88.17%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5599 55.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9041 90.41%
OATP1B3 inhibitior + 0.9538 95.38%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6530 65.30%
P-glycoprotein inhibitior - 0.8915 89.15%
P-glycoprotein substrate - 0.9255 92.55%
CYP3A4 substrate - 0.5054 50.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7903 79.03%
CYP3A4 inhibition - 0.7733 77.33%
CYP2C9 inhibition - 0.6401 64.01%
CYP2C19 inhibition - 0.5998 59.98%
CYP2D6 inhibition - 0.9053 90.53%
CYP1A2 inhibition + 0.8746 87.46%
CYP2C8 inhibition - 0.6917 69.17%
CYP inhibitory promiscuity + 0.6550 65.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8109 81.09%
Carcinogenicity (trinary) Warning 0.4178 41.78%
Eye corrosion - 0.9619 96.19%
Eye irritation + 0.8016 80.16%
Skin irritation - 0.7657 76.57%
Skin corrosion - 0.9473 94.73%
Ames mutagenesis + 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6569 65.69%
Micronuclear + 0.7233 72.33%
Hepatotoxicity + 0.6963 69.63%
skin sensitisation - 0.8222 82.22%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.6455 64.55%
Acute Oral Toxicity (c) III 0.6831 68.31%
Estrogen receptor binding + 0.9086 90.86%
Androgen receptor binding + 0.5892 58.92%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7689 76.89%
Aromatase binding + 0.7547 75.47%
PPAR gamma - 0.6201 62.01%
Honey bee toxicity - 0.8415 84.15%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.8036 80.36%

Targets

Top

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 98.46% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.58% 86.33%
CHEMBL2581 P07339 Cathepsin D 91.31% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.27% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.20% 91.11%
CHEMBL240 Q12809 HERG 86.27% 89.76%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.47% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.65% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 80.66% 94.73%

Plants that contains it

Top
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 euchrestifolia
Murraya koenigii

Cross-Links

Top
PubChem 11736261
LOTUS LTS0045098
wikiData Q105151440