Hétérocycles azotés (N)

8-Bromoadenine is a nucleophile that reacts with electrophiles to form adducts. 8-Bromoadenine has been shown to induce DNA strand breaks and oxidative damage in vitro, which may be due to its ability to react with DNA bases and form intramolecular hydrogen bonds. 8-Bromoadenine has also been shown to cause inflammatory bowel disease in mice by increasing the production of proinflammatory cytokines. 8-Bromoadenine induces Toll-like receptor 4 (TLR4) signaling, which leads to enhancement of radiation response. This drug can also be used as the monosodium salt for treating cancer, although it only has a limited number of sequences that can be synthesized.

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2-Pyrimidinecarboxaldehyde is a nitrogen heterocyclic compound that is found in many biological systems. 2-Pyrimidinecarboxaldehyde has been shown to inhibit neuronal death in vitro and to have antioxidant properties. It also has been shown to be toxic for fetal bovine and human cells. 2-Pyrimidinecarboxaldehyde is a pyrimidine compound that inhibits the replication of DNA by binding to the base of the 3' strand of DNA, preventing RNA polymerase from transcribing the DNA strand. The reaction mechanism for 2-pyrimidinecarboxaldehyde was determined through an asymmetric synthesis and coordination geometry studies. 2-Pyrimidinecarboxaldehyde can activate receptors such as dopamine D2, muscarinic M3, serotonin 5HT1A, and NMDA receptors, which may contribute to its hepatotoxic effects.

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3-(4-Methylpiperazin-1-yl)propan-1-amine is a molecule that has been shown to have therapeutic potential for the treatment of glioma, neurodegenerative diseases, and cancer. 3-(4-Methylpiperazin-1-yl)propan-1-amine is taken up by cells via endocytosis and inhibits the expression of cellular pluripotency markers. The drug also has an antiviral effect against herpes simplex virus type 1 and 2, which are viruses that cause cold sores and genital herpes respectively. 3-(4-Methylpiperazin-1-yl)propan-1-amine is biodegradable, chemically stable, and can be used in regenerative medicine.

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Methyl 4-(4-pyridinyl)benzoate is a ligand that selectively binds to the axial site of the metal ion. The coordination of this ligand is supramolecular and tetracarboxylate. It has an axial ligand with a square geometry and a carboxylate group at its axial position. Methyl 4-(4-pyridinyl)benzoate coordinates to the metal ion in an axial fashion, which allows for selective binding to various metal ions.

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