He, Zhangxu team published research on European Journal of Medicinal Chemistry in 2019 | 31181-90-5

31181-90-5, 5-Bromopyridine-2-carbaldehyde is a useful research compound. Its molecular formula is C6H4BrNO and its molecular weight is 186.01 g/mol. The purity is usually 95%.

5-Bromopyridine-2-carbaldehyde is a water soluble organic molecule that has been shown to inhibit the mitochondrial respiratory chain. It is a structural analog of the natural substrate for mitochondrial cytochrome c oxidase, 5-aminolevulinic acid. This compound has been shown to be selective against cancer cells and has anti-viral properties. The photophysical properties of 5-bromopyridine-2-carbaldehyde have been studied extensively. The fluorescence quantum yield of this molecule in aqueous solution is 0.06%., Application of C6H4BrNO

Pyridine has a conjugated system of six π electrons that are delocalized over the ring. 31181-90-5, formula is C6H4BrNO, Name is 5-Bromopicolinaldehyde. The molecule is planar and, thus, follows the Hückel criteria for aromatic systems. Application of C6H4BrNO.

He, Zhangxu;Qiao, Hui;Yang, Feifei;Zhou, Wenjuan;Gong, Yunpeng;Zhang, Xinhui;Wang, Haojie;Zhao, Bing;Ma, Liying;Liu, Hong-min;Zhao, Wen research published 《 Novel thiosemicarbazone derivatives containing indole fragment as potent and selective anticancer agent》, the research content is summarized as follows. A series of novel thiosemicarbazone derivatives I [R1 = Ph, benzyl, phenylethyl,etc.; R2 = 2-pyridyl, 3-methyl-2-pyridyl, 4-methyl-2-pyridyl,etc.; R3 = H, Me] containing indole fragment were designed and synthesized. Most compounds exhibited excellent antiproliferative activity against PC3, MGC803 and EC109 cell lines with low micromolar IC50 (0.14-12μM). Especially, compound I [R1 = 2-(5-chloro-1H-indol-3-yl)ethyl; R2 = 5-methyl-2-pyridyl; R3 = H] can selectively inhibit PC3 cells in three tested tumor cells with IC50 value of 0.14 μM, which was attributed to a synergistic effect after introducing indole fragment into the TSC structure. Meanwhile, compound I [R1 = 2-(5-chloro-1H-indol-3-yl)ethyl; R2 = 5-methyl-2-pyridyl; R3 = H] displayed more selectivity in PC3 cells toward two normal WPMY-1 and GES-1 cell lines, compared to those of 3-AP and DPC. It was also found that I [R1 = 2-(5-chloro-1H-indol-3-yl)ethyl; R2 = 5-methyl-2-pyridyl; R3 = H] can effectively inhibit PC3 cell proliferation, colonization and induce apoptosis. Compound I [R1 = 2-(5-chloro-1H-indol-3-yl)ethyl; R2 = 5-methyl-2-pyridyl; R3 = H] may significantly suppress migration and invasion by blocking the EMT process but had no effect on cell cycle. Collectively, this findings indicated that I [R1 = 2-(5-chloro-1H-indol-3-yl)ethyl; R2 = 5-methyl-2-pyridyl; R3 = H] with structure of thiosemicarbazone containing indole may serve as a useful anticancer lead for further optimization and development.

31181-90-5, 5-Bromopyridine-2-carbaldehyde is a useful research compound. Its molecular formula is C6H4BrNO and its molecular weight is 186.01 g/mol. The purity is usually 95%.

5-Bromopyridine-2-carbaldehyde is a water soluble organic molecule that has been shown to inhibit the mitochondrial respiratory chain. It is a structural analog of the natural substrate for mitochondrial cytochrome c oxidase, 5-aminolevulinic acid. This compound has been shown to be selective against cancer cells and has anti-viral properties. The photophysical properties of 5-bromopyridine-2-carbaldehyde have been studied extensively. The fluorescence quantum yield of this molecule in aqueous solution is 0.06%., Application of C6H4BrNO

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem