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C43H55NO15 is a macrolide antibiotic, a chemical compound with a molecular formula consisting of 43 carbon atoms, 55 hydrogen atoms, one nitrogen atom, and 15 oxygen atoms. It features a large lactone ring and various functional groups that enable it to bind to and inhibit bacterial ribosomes, thereby disrupting protein synthesis and leading to bacterial cell death. C43H55NO15 holds significant medical importance due to its wide application in treating bacterial infections.

1385028-85-2

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1385028-85-2 Usage

Uses

Used in Pharmaceutical Industry:
C43H55NO15 is used as an antibiotic for treating a broad spectrum of bacterial infections. Its ability to inhibit bacterial protein synthesis makes it an effective agent against various pathogens, contributing to its widespread use in medical treatments.
Used in Research and Development:
In the field of microbiology and pharmaceutical research, C43H55NO15 serves as a subject for studying the mechanisms of antibiotic action and resistance development in bacteria. This research is crucial for the development of new antibiotics and strategies to combat antibiotic resistance.
Used in Diagnostic Applications:
C43H55NO15 can be utilized in diagnostic tests to identify the presence of specific bacteria or to assess the effectiveness of antibiotic treatments. Its interaction with bacterial ribosomes can be leveraged to determine the susceptibility of bacterial strains to this class of antibiotics.
Used in Veterinary Medicine:
Similar to its use in human medicine, C43H55NO15 is also employed in veterinary medicine to treat bacterial infections in animals. Its broad-spectrum activity makes it a valuable tool for managing infections in various animal species.
Used in Agricultural Applications:
In agriculture, C43H55NO15 may be used to combat bacterial infections in crops or livestock, contributing to disease management and food safety. Its application in this field can help maintain crop health and productivity, as well as ensure the well-being of farm animals.

Check Digit Verification of cas no

The CAS Registry Mumber 1385028-85-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,5,0,2 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1385028-85:
(9*1)+(8*3)+(7*8)+(6*5)+(5*0)+(4*2)+(3*8)+(2*8)+(1*5)=172
172 % 10 = 2
So 1385028-85-2 is a valid CAS Registry Number.

1385028-85-2Upstream product

1385028-85-2Downstream Products

1385028-85-2Relevant academic research and scientific papers

A selective intramolecular transacylation of taxoids accompanying with the oxetane ring opening

Gao, Feng,Yu, Min,Chen, Qiao-Hong,Wang, Feng-Peng

, p. 415 - 418 (2012)

A selective intramolecular transacylation from C-4 to C-5 of taxoids, which occurred simultaneously with the oxetane D-ring opening and was promoted by TiCl4, was presented. The optimal condition was found to be treatment of substrates in doubl

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