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• W2022995312 abstract "Abstract Several 3‐heteroaryl analogs of the known dehydroquinase inhibitor (1R,4R,5R)‐1,4,5‐trihydroxy‐2‐cyclohexene‐1‐carboxylic acid ( 4 ) were synthesized and tested as inhibitors of Helicobacter pylori type II dehydroquinase, the third enzyme of the shikimic acid pathway. All of these compounds proved to be reversible competitive inhibitiors of this enzyme and proved to be, with the exception of nitrile 8 e , more potent than the parent inhibitor 4 (K i =370 μ M ). The 2‐thienyl derivative 8 b was found to be the most potent inhibitor of the series and has a K i value of 540 n M , which is almost seven hundred times lower than that of the parent inhibitor. The 3‐nitrothienyl derivative 8 d and 2‐furanyl derivative 8 a also had a good affinity of 1 μ M . The conformation of the potent competitive inhibitor 8 b , when bound in the active site of the H. pylori enzyme, was elucidated by 1D‐selective inversion NOE, Saturation Transfer Difference (STD) and transferred NOESY NMR experiments. One of the conformations that exists in solution for the potent competitive inhibitor 2‐thienyl derivative 8 b is selected when it is bound to the active site of the enzyme. In the bound conformation derivative 8 b has the sulfur atom of its thienyl group oriented towards the double bond of the cyclohexene moiety. The large STD effects observed for the aromatic protons of 8 b show that it is the thiophene side of the ligand that makes closest contact with enzyme protons. Docking studies using GOLD3.0.1 suggest that the conformation determined by NMR allows strong lipophilic interactions with the enzyme residues Pro9, Asn10, Ile11, Gly78 and Ala 79. Competitive STD experiments carried out with high‐, medium‐ and low‐affinity ligands 8 b , 5 d and 5 f show that they all bind in the same site of Helicobacter pylori dehydroquinase." @default.
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• W2022995312 date "2008-05-08" @default.
• W2022995312 modified "2023-10-16" @default.
• W2022995312 title "Competitive Inhibitors ofHelicobacter pylori Type II Dehydroquinase: Synthesis, Biological Evaluation, and NMR Studies" @default.
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• W2022995312 doi "https://doi.org/10.1002/cmdc.200700307" @default.
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