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6018-52-6

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6018-52-6 Usage

Description

(-)-(1R,5S)-N-acetyl-1,2,3,4,5,6-hexahydro-1,5-methano-pyrido-[1,2-a][1,5]diazocin-8-one, also known as N-1,5a-methanomethylbrevicidin, is a complex chemical compound derived from the naturally occurring alkaloid brevicidin. It features a unique molecular structure and possesses potent inhibitory activity against microbial peptide deformylases, which are essential for bacterial protein synthesis. This makes it a promising candidate for the development of novel antibiotics to combat drug-resistant infections.

Uses

Used in Pharmaceutical Industry:
N-1,5a-methanomethylbrevicidin is utilized as a lead compound in the development of new antibiotics. Its ability to inhibit microbial peptide deformylases makes it a potential alternative or adjunct to existing antibiotic treatments, particularly for drug-resistant bacterial strains. (-)-(1R,5S)-N-acetyl-1,2,3,4,5,6-hexahydro-1,5-methano-pyrido-[1,2-a][1,5]diazocin-8-one's unique structure and activity also make it a valuable target for further research and optimization in medicinal chemistry to enhance its efficacy and safety.
Used in Chemical Synthesis:
Due to its complex molecular structure, N-1,5a-methanomethylbrevicidin serves as an important target for chemical synthesis research. Scientists are interested in exploring various synthetic routes and methods to efficiently produce this compound, as well as its analogs and derivatives, to better understand its structure-activity relationship and to potentially discover new antibiotics with improved properties.
Used in Medicinal Chemistry Research:
N-1,5a-methanomethylbrevicidin is a valuable subject of study in medicinal chemistry, as its unique structure and activity provide insights into the design and development of new antimicrobial agents. Researchers are investigating its binding interactions with peptide deformylases, as well as its potential synergistic effects with other antibiotics, to optimize its therapeutic potential and guide the discovery of new drugs targeting bacterial protein synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 6018-52-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,1 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6018-52:
(6*6)+(5*0)+(4*1)+(3*8)+(2*5)+(1*2)=76
76 % 10 = 6
So 6018-52-6 is a valid CAS Registry Number.

6018-52-6Upstream product

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