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Syntheses and Biological Activities of Ethyl N-Hydroxy-N-(substituted)phenyloxamates as KARI Inhibitors

Syntheses and Biological Activities of Ethyl N-Hydroxy-N-(substituted)phenyloxamates as KARI Inhibitors
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摘要 Nine ethyl N-hydroxy-N-(substituted) phenyloxamates (2a-2i), based on the structure of the KARI inhibitor IpOHA, were synthesized. Their structures were established on the bases of 1^H NMR, IR, ESI-MS and elemental analyses. Among the nine compounds, four show in vitro inhibitory activity on rice KARI, with 2c and 2g[ Ki values of (35.2±4.9) and (49.4 ±6. 3) μmol/L] having similar activity to the precursor of IpOHA(A, Ki =34. 1±6. 7 μmol/L). The results will be helpful to further molecular design of more potent KARI inhibitors. Nine ethyl N-hydroxy-N-(substituted) phenyloxamates (2a-2i), based on the structure of the KARI inhibitor IpOHA, were synthesized. Their structures were established on the bases of 1^H NMR, IR, ESI-MS and elemental analyses. Among the nine compounds, four show in vitro inhibitory activity on rice KARI, with 2c and 2g[ Ki values of (35.2±4.9) and (49.4 ±6. 3) μmol/L] having similar activity to the precursor of IpOHA(A, Ki =34. 1±6. 7 μmol/L). The results will be helpful to further molecular design of more potent KARI inhibitors.
出处 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2007年第3期280-283,共4页 高等学校化学研究(英文版)
基金 Supported by the National Basic Research Program of China(No2003CB114406) the National Natural Science Foundationof China(Key Project No20432010)
关键词 KARI inhibitor IpOHA Phenyloxamate Synthesis Biological activity KARI inhibitor IpOHA Phenyloxamate Synthesis Biological activity
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