99009-85-5Relevant articles and documents
Synthesis of quinoline based molecular probes for detection of nitric oxide
Kansal, Sushil K.,Kaur, Manpreet,Kaushik, Deepender,Mehta, Surinder K.,Mutreja, Vishal,Pathania, Khushboo,Pawar, Sandip V.,Sahoo, Subash Chandra,Saini, Vaneet,Salunke, Deepak B.
, (2022/03/31)
Nitric oxide (NO), an important signaling molecule of the immune, vascular and nervous system was found to be present in different concentrations in biological fluids such as blood and plasma as well as in neural tissue and endothelium. A variety of competent probes may be required to detect NO and understand its complicated biochemistry, and establish the correlation of its concentrations among different biological media to its biological effect. In order to find new probes as NO sensors, four quinoline-derived ortho-diamines were synthesized and their structures and purities were confirmed by various spectroscopic methods including single-crystal X-ray diffraction. The molecules were investigated for the bimodal sensing (UV–visible and fluorescence) potential for NO. All the probes have showcased both UV–visible and fluorescent signals towards the presence of NO due to the formation of corresponding triazoles. Interestingly, the limit of detection was observed in the nanomolar range (56.1–95 nM) for the four ligands using colorimetric signals. Among the prepared molecules, the N4-(4-chlorobenzyl)quinoline-3,4-diamine exhibited superior sensing parameters viz the limit of detection (LOD), formation constant (Kf), and quenching constant (Ksv). An isolated triazole further confirmed the proposed mechanism of NO detection.
High Turnover Pd/C Catalyst for Nitro Group Reductions in Water. One-Pot Sequences and Syntheses of Pharmaceutical Intermediates
Gallou, Fabrice,Li, Xiaohan,Lipshutz, Bruce H.,Takale, Balaram S.,Thakore, Ruchita R.
supporting information, p. 8114 - 8118 (2021/10/25)
Commercially available Pd/C can be used as a catalyst for nitro group reductions with only 0.4 mol % Pd loading. The reaction can be performed using either silane as a transfer hydrogenating agent or simply a hydrogen balloon (μ1 atm pressure). With this technology, a series of nitro compounds was reduced to the desired amines in high chemical yields. Both the catalyst and surfactant were recycled several times without loss of reactivity.
AMINE COMPOUNDS HAVING ANTI-INFLAMMATORY, ANTIFUNGAL, ANTIPARASITIC AND ANTICANCER ACTIVITY
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Page/Page column 174, (2014/08/19)
Amine compounds having activity against inflammation, fungi, unicellular parasitic microorganisms, and cancer are described. The compounds contain a monocyclic, bicyclic, or tricyclic aromatic ring having one, two, or three ring nitrogen atoms.
