N-Ethylcarbazole-3-carboxaldehyde

CAS : 7570-45-8

Ref. 3D-FE62359

Informations sur le produit

• Nom: N-Ethylcarbazole-3-carboxaldehyde
• Synonymes: 3-Formyl-N-ethylcarbazole, 10-Ethyl-10H-carbazole-3-carbaldehyede, 3-Formyl-9-ethylcarbazole, 9-Ethyl-3-carbazolecarboxaldehyde, 9-Ethyl-3-formyl-9H-carbazole, 9-Ethyl-3-formylcarbazole, 9-Ethyl-9H-carbazole-3-aldehyde, 9-Ethyl-9H-carbazole-3-carboxaldehyde, 9-Ethylcarbazole-3-carbaldehyde, 9-ethyl-9H-carbazole-3-carbaldehyde, 9H-Carbazole-3-carboxaldehyde, 9-ethyl-, Carbazole-3-carboxaldehyde, 9-ethyl-, N-Ethyl-9H-carbazole-3-aldehyde, N-Ethylcarbazol-3-aldehyde, N-ethyl-3-formylcarbazole, N-ethylcarbazole-3-aldehyde, N-ethylcarbazole-3-carbaldehyde, NSC 231558
• CAS: 7570-45-8

Description

N-Ethylcarbazole-3-carboxaldehyde is an organic compound that has been shown to have anti-cancer properties. It activates the enzyme dioxygenase, which in turn generates reactive oxygen species (ROS) that induce DNA damage and apoptosis in mammalian cells. The photophysical and fluorescence spectrometry of N-ethylcarbazole-3-carboxaldehyde were studied as a function of pH and found to be sensitive to acidic environments. N-Ethylcarbazole-3-carboxaldehyde is also able to form covalent bonds with DNA bases, leading to irreversible oxidation.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 223.27 g/mol
• Formule: C₁₅H₁₃NO
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C15H13NO/c1-2-16-14-6-4-3-5-12(14)13-9-11(10-17)7-8-15(13)16/h3-10H,2H2,1H3
• Code InChI: InChIKey=QGJXVBICNCIWEL-UHFFFAOYSA-N
• SMILES: CCn1c2ccccc2c2cc(C=O)ccc21