74274-72-9 Usage
Chemical structure
1-ethenyl-6-fluoro-7-(4-methylpiperazin-1-yl)-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid is a complex organic compound with a specific arrangement of atoms and functional groups.
Classification
It is a quinolone antibiotic, which is a type of antibiotic that targets bacterial DNA replication and repair processes.
Function
The compound is used to treat a variety of bacterial infections by inhibiting the growth and replication of bacteria, ultimately leading to their destruction.
Effectiveness
It is effective against a wide range of gram-positive and gram-negative bacteria, including strains that are resistant to other antibiotics.
Mechanism of action
The antibiotic works by targeting bacterial DNA gyrase and topoisomerase IV, which are essential enzymes involved in the replication and repair of bacterial DNA.
Safety
Its broad spectrum of activity, combined with its relatively low toxicity to human cells, makes it a valuable and widely-used antibiotic in the treatment of various infections.
Check Digit Verification of cas no
The CAS Registry Mumber 74274-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,7 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74274-72:
(7*7)+(6*4)+(5*2)+(4*7)+(3*4)+(2*7)+(1*2)=139
139 % 10 = 9
So 74274-72-9 is a valid CAS Registry Number.
74274-72-9Relevant academic research and scientific papers
Pyridonecarboxylic acids as antibacterial agents. 2. Synthesis and structure-activity relationships of 1,6,7-trisubstituted 1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acids, including enoxacin, a new antibacterial agent
Matsumoto,Miyamoto,Minamida,Nishimura,Egawa,Nishimura
, p. 292 - 301 (2007/10/02)
The title compounds having nitro, amino, cyano, chloro, or fluoro as the C-6 substituent were prepared. Introduction of the chloro and cyano groups at C-6 was accomplished by the Sandmeyer reaction of 6-amino-1,8-naphthyridine derivatives via their 6-diaz
