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1139906-49-2

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1139906-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1139906-49-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,9,9,0 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1139906-49:
(9*1)+(8*1)+(7*3)+(6*9)+(5*9)+(4*0)+(3*6)+(2*4)+(1*9)=172
172 % 10 = 2
So 1139906-49-2 is a valid CAS Registry Number.

1139906-49-2Downstream Products

1139906-49-2Relevant academic research and scientific papers

Synthesis and antibacterial activities of novel tyrocidine A glycosylated derivatives towards multidrug-resistant pathogens

Zou, Yan,Zhao, Qingjie,Zhang, Chunmei,Wang, Liang,Li, Wenjuan,Li, Xiang,Wu, Qiuye,Hu, Honggang

, p. 586 - 592 (2015/07/02)

Glycosylation can have a multifaceted impact on the properties and functions of peptides and plays a critical role in interacting with or binding to the target molecules. Herein, based on the previously reported method for macrocyclic glycopeptide synthesis, two series of tyrocidine A glycosylated derivatives (1a-f and 2a-f) were synthesized and evaluated for their antibacterial activities to further study the structure and activity relationships (SAR). Biological studies showed that the synthetic glycosylated derivatives had good antibacterial activities towards methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus. SAR studies based on various glycans and linkages were used to enhance the biochemical profile, resulting in the identification of several potent antibiotics, such as 1f, with a great improved therapeutic index than tyrocidine A.

Synthesis and antibacterial activities of N-Glycosylated derivatives of tyrocidine a, a macrocyclic peptide antibiotic

Honggang, Hu,Jie, Xue,Swarts, Benjamin M.,Qianli, Wang,Qiuye, Wu,Zhongwu, Guo

experimental part, p. 2052 - 2059 (2009/12/30)

An efficient and practical method for macrocyclic glycopeptide synthesis was developed and utilized to synthesize tyrocidine A and its glycosylated derivatives. The method is based on solid-phase peptide synthesis using 2-chlorotrityl resin as the solid-phase support and glycosyl amino acids as building blocks. After glycopeptides with fully protected glycans and side chains were released from the acid-labile resin, their Cand N-termini were intramolecularly coupled in solution to afford cyclic glycopeptides in quantitative yields. This synthetic method should be generally applicable to various macrocyclic glycopeptides. Biological studies of the synthetic tyrocidine A derivatives showed that linking glycans directly to the Asn residue of tyrocidine A diminished its antibacterial activity, but linking glycans to Asn via a simple spacer did not. These results Revealed the important impact of glycans on the activities, and probably the structures, of glycopeptide antibiotics.

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