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400073-80-5

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400073-80-5 Usage

Structure

Benzimidazole derivative with a trifluoromethylphenyl group attached to the 2-position of the benzimidazole ring

Properties

Potential pharmaceutical and medicinal properties: Studied as an antifungal and antiproliferative agent
Structure and chemical properties: Make it a promising candidate for further research and development in drug discovery and medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 400073-80-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,0,7 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 400073-80:
(8*4)+(7*0)+(6*0)+(5*0)+(4*7)+(3*3)+(2*8)+(1*0)=85
85 % 10 = 5
So 400073-80-5 is a valid CAS Registry Number.

400073-80-5Relevant articles and documents

Development of benzimidazole-based derivatives as antimicrobial agents and their synergistic effect with colistin against gram-negative bacteria

Dokla, Eman M.E.,Abutaleb, Nader S.,Milik, Sandra N.,Li, Daoyi,El-Baz, Karim,Shalaby, Menna-Allah W.,Al-Karaki, Rawan,Nasr, Maha,Klein, Christian D.,Abouzid, Khaled A.M.,Seleem, Mohamed N.

, (2020)

Gram-negative bacteria pose a distinctive risk worldwide, especially with the evolution of major resistance to carbapenems, fluoroquinolones and colistin. Therefore, development of new antibacterial agents to target Gram-negative infections is of utmost importance. Using phenotypic screening, we synthesized and tested thirty-one benzimidazole derivatives against E. coli JW55031 (TolC mutant strain). Compound 6c showed potent activity with MIC value of 2 μg/ml, however, it lacked activity against several Gram-negative microbes with intact efflux systems, including E. coli BW25113 (wild-type strain). Combination of 6c with colistin partially restored its antibacterial activity against wild strains (MIC range, 8–16 μg/ml against E. coli, K. pneumoniae, A. baumannii, and P. aeruginosa). 6c exhibited no cytotoxicity against two mammalian cell lines. Therefore, compound 6c represents a promising lead for further optimization to overcome Gram-negative resistance alone or in combination therapy.

2-ARYLBENZIMIDAZOLES AS PPARGC1A ACTIVATORS FOR TREATING NEURODEGENERATIVE DISEASES

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Paragraph 85; 90, (2020/03/02)

A genus of compounds encompassed by formula (III) and their use is disclosed: Formula (III). The compounds activate Ppargc1a and, as a consequence, are useful for treating a variety of neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS), Alzheimer's disease, Parkinson's disease, Huntington's disease, frontotemporal degeneration, dementia with Lewy bodies, motor neuron diseases, and a demyelinating disease.

Fluoro-benzimidazole derivatives to cure Alzheimer's disease: In-silico studies, synthesis, structure-activity relationship and in vivo evaluation for β secretase enzyme inhibition

Ali, Sayyad,Asad, Muhammad Hassham Hassan Bin,Maity, Soham,Zada, Wahid,Rizvanov, Albert A.,Iqbal, Jamshed,Babak, Borhan,Hussain, Izhar

, (2019/05/04)

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