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2-[3-(2-amino-4-methyl-pentanoylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

473710-40-6

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  • 2-[3-(2-amino-4-methyl-pentanoylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester

    Cas No: 473710-40-6

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  • 2-[3-(2-amino-4-methyl-pentanoylamino)-propylamino]-3-{3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-[3-(4-methoxy-benzyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-2-yl}-3-hydroxy-propionic acid tert-butyl ester

    Cas No: 473710-40-6

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473710-40-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 473710-40-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,7,1 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 473710-40:
(8*4)+(7*7)+(6*3)+(5*7)+(4*1)+(3*0)+(2*4)+(1*0)=146
146 % 10 = 6
So 473710-40-6 is a valid CAS Registry Number.

473710-40-6Relevant articles and documents

Improved convergent synthesis of 5'-epi-analogues of muraymycin nucleoside antibiotics

Spork, Anatol P.,Koppermann, Stefan,Ducho, Christian

scheme or table, p. 2503 - 2507 (2010/01/16)

Nucleoside antibiotics represent a promising class of natural products for the development of novel antibacterial agents, with particular respect to structurally simplified analogues maintaining biological activity. There are established truncated 5-epi-d

Muraymycins, novel peptidoglycan biosynthesis inhibitors: Synthesis and SAR of their analogues

Yamashita, Ayako,Norton, Emily,Petersen, Peter J.,Rasmussen, Beth A.,Singh, Guy,Yang, Youjin,Mansour, Tarek S.,Ho, Douglas M.

, p. 3345 - 3350 (2007/10/03)

A series of Muraymycin analogues was synthesized. These analogues showed excellent antimicrobial activity against gram-positive organisms. These analogues also showed excellent inhibitory activity against the target peptidoglycan biosynthesis enzyme MraY,

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