cas 1021075-63-7|| where to buy 8-ethoxy-2-oxo-N-[3-(6-oxo-3-phenyl-1,6-dihydropyridazin-1-yl)propyl]-2H-chromene-3-carboxamide

Nombre del producto:8-ethoxy-2-oxo-N-[3-(6-oxo-3-phenyl-1,6-dihydropyridazin-1-yl)propyl]-2H-chromene-3-carboxamide

IUPAC Name:8-ethoxy-2-oxo-N-[3-(6-oxo-3-phenyl-1,6-dihydropyridazin-1-yl)propyl]-2H-chromene-3-carboxamide

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: Núm. De CAS :1021075-63-7; Fórmula molecular:C25H23N3O5; Punto de fusión:-; Código de sonrisas:CCOC1=C2OC(=O)C(=CC2=CC=C1)C(=O)NCCCN1N=C(C=CC1=O)C1=CC=CC=C1; Densidad:

: Número de catálogo:CM636347; Peso molecular:445.48; Punto de ebullición:; Nº Mdl:; Almacenamiento:

: Pyridazines; Pyridazine, also known as o-diazobenzene, is a six-membered heterocyclic compound containing two nitrogen heteroatoms in the 1 and 2 positions with a special structure and a wide biological activity. Pyridazine is more and more popular in drug development, and a variety of pyridazine drugs have been developed and marketed. From the perspective of the therapeutic field, pyridazine drug molecules are mainly used for tumor treatment, but also involve in many therapeutic fields such as inflammation, hypertension and cardiovascular disease. With the increase and in-depth of research, pyridazine drugs will play more roles in the treatment of diseases.

: Coumarins; Coumarin occurs naturally in a variety of plants, such as lentils, sweet sawdust, vanilla grass, and sweet grass. Coumarin has a simple structure, benzopyrone, associated with different reaction centers. Coumarins are further subdivided into different classes: simple coumarins, pyranocoumarins, furanocoumarins, dicoumarins and isocoumarins. Coumarin derivatives are an important class of natural plant metabolites with various biological activities. They can also be synthesized artificially, and various synthetic coumarin derivatives (azoles, sulfonyls, furans, pyrazoles, etc.) have shown good anticancer, antitumor and antiproliferative activities. Coumarin derivatives are not only effective anticancer agents, but also possess minimum side effects. Based on different substitution patterns, these potential active substances show a great ability to modulate potential anticancer activities.