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1456774-83-6

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1456774-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1456774-83-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,6,7,7 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1456774-83:
(9*1)+(8*4)+(7*5)+(6*6)+(5*7)+(4*7)+(3*4)+(2*8)+(1*3)=206
206 % 10 = 6
So 1456774-83-6 is a valid CAS Registry Number.

1456774-83-6Downstream Products

1456774-83-6Relevant academic research and scientific papers

BROAD SPECTRUM ANTIBIOTIC ARYLOMYCIN ANALOGS

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Page/Page column 154; 155, (2013/09/26)

Arylomycin analogs are provided, wherein the analogs can have broad spectrum bioactivity. Resistance to the antibiotic bioactivity of natural product arylomycin in a range of pathogenic bacterial species has been found to depend upon single amino acid mutations at defined positions of bacterial Signal Peptidases (SPases), wherein the presence of a proline residue confers arylomycin resistance. Arylomycin analogs are provided herein that can overcome that resistance and provide for a broader spectrum of antibiotic bioactivity than can natural product arylomycins such as arylomycin A2. Methods for determining if a bacterial strain is susceptible to narrow spectrum arylomycin antibiotics, or if a broad spectum analog is required for treatment, is provided. Pharmaceutical compositions and methods of treatment of bacterial infections, and methods of synthesis of arylomycin analogs, are provided.

Efforts toward broadening the spectrum of arylomycin antibiotic activity

Liu, Jian,Smith, Peter A.,Steed, Danielle Barrios,Romesberg, Floyd

supporting information, p. 5654 - 5659 (2013/10/01)

New antibiotics are needed, and one source may be 'latent' antibiotics, natural products whose once broad-spectrum activity is currently limited by the evolution of resistance in nature. We have identified a potential class of latent antibiotics, the arylomycins, which are lipopeptides with a C-terminal macrocycle that target signal peptidase and whose spectrum is limited by a resistance-conferring mutation in many bacteria. Herein, we report the synthesis and evaluation of several arylomycin derivatives, and demonstrate that both C-terminal homologation with a glycyl aldehyde and addition of a positive charge to the macrocycle increase the activity and spectrum of the arylomycin scaffold.

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