Autor: |
Michael J. Miller, C. Y. Han, Kenneth J. Gruys, James A. Sikorski, Ko-Chung Lin, Joel E. Ream, Paul D. Pansegrau, D. G. Cleary, Mark C. Walker, Diane Susan Braccolino, Dora M. Schnur, Jose L. Font, Susan D. Corey, Ajit S. Shah |
Rok vydání: |
2010 |
Předmět: |
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Zdroj: |
ChemInform. 24 |
ISSN: |
0931-7597 |
DOI: |
10.1002/chin.199335301 |
Popis: |
Novel aromatic bisubstrate inhibitors of the enzyme EPSP (5-enolpyruvoylshikimate-3-phosphate) synthase (EC 2.5.1.19) have been designed and synthesized as structural analogs of the single, catalytic intermediate 1 utilized by the enzyme. These aromatic inhibitors incorporate novel α-hydroxyphosphonates, malonate ethers and α-hydroxymalonates as replacements for the hydrolytically labile 3-phosphate group. These 3-phosphate mimics were much preferred to the corresponding methylene and vinylic phosphonates, malonates and phosphonomethyl ethers. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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