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N'-(2-hydroxy-5-nitrobenzylidene)-2-(4-methoxyphenyl)acetyl hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41377-58-6

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41377-58-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41377-58-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,7 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41377-58:
(7*4)+(6*1)+(5*3)+(4*7)+(3*7)+(2*5)+(1*8)=116
116 % 10 = 6
So 41377-58-6 is a valid CAS Registry Number.

41377-58-6Downstream Products

41377-58-6Relevant academic research and scientific papers

Benzaldehyde Schiff bases regulation to the metabolism, hemolysis, and virulence genes expression in vitro and their structure-microbicidal activity relationship

Xia, Lei,Xia, Yu-Fen,Huang, Li-Rong,Xiao, Xiao,Lou, Hua-Yong,Liu, Tang-Jingjun,Pan, Wei-Dong,Luo, Heng

, p. 83 - 93 (2015)

There is an urgent need to develop new antibacterial agents because of multidrug resistance by bacteria and fungi. Schiff bases (aldehyde or ketone-like compounds) exhibit intense antibacterial characteristics, and are therefore, promising candidates as antibacterial agents. To investigate the mechanism of action of newly designed benzaldehyde Schiff bases, a series of high-yielding benzaldehyde Schiff bases were synthesized, and their structures were determined by NMR and MS spectra data. The structure-microbicidal activity relationship of derivatives was investigated, and the antibacterial mechanisms were investigated by gene assays for the expression of functional genes in vitro using Escherichia coli, Staphylococcus aureus, and Bacillus subtilis. The active compounds were selective for certain active groups. The polar substitution of the R2 group of the amino acids in the Schiff bases, affected the antibacterial activity against E. coli and S. aureus; specific active group at the R3 or R4 groups of the acylhydrazone Schiff bases could improve their inhibitory activity against these three tested organisms. The antibacterial mechanism of the active benzaldehyde Schiff bases appeared to regulate the expression of metabolism-associated genes in E. coli, hemolysis-associated genes in B. subtilis, and key virulence genes in S. aureus. Some benzaldehyde Schiff bases were bactericidal to all the three strains and appeared to regulate gene expression associated with metabolism, hemolysis, and virulence, in vitro. The newly designed benzaldehyde Schiff bases possessed unique antibacterial activity and might be potentially useful for prophylactic or therapeutic intervention of bacterial infections.

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