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Molbank 2015, 2015(2), M864;


Department of Medicinal Chemistry, College of Pharmacy, University of Florida, Gainesville, FL 32610, USA
Author to whom correspondence should be addressed.
Received: 4 April 2015 / Revised: 1 June 2015 / Accepted: 5 June 2015 / Published: 17 June 2015
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Aminoacyl sulfamides represent a family of high-affinity inhibitors of the specific aminoacyl tRNA synthetase activity. In this paper we describe the synthesis of a novel sulfamide adenosine derivative 4 bearing pyroglutamyl fragment (pGlu-SA). View Full-Text
Keywords: aminoacyl sulfamide; tRNA synthetase inhibitor; pGlu-SA aminoacyl sulfamide; tRNA synthetase inhibitor; pGlu-SA

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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).

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Khaybullin, R.N.; Liang, X.; Qi, X. (S)-N-(N-(((2R,3S,4R,5R)-5-(6-Amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)sulfamoyl)-5-oxopyrrolidine-2-carboxamide. Molbank 2015, 2015, M864.

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