Title : Synthesis and Aldose Reductase Inhibitory Activity of Botryllazine A Derivatives.

Pub. Date : 2019

PMID : 31155561






2 Functional Relationships(s)
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1 Analogues possessing aromatic bicyclic systems at the C5 position of the central pyrazine ring exhibited superior AR inhibiting activity relative to the parent botryllazine A. Pyrazines aldo-keto reductase family 1 member B Homo sapiens
2 Conversely, a benzoyl group-containing phenolic hydroxyl groups-at either position C2 or C3 of the pyrazine ring was essential for attainment of high inhibitory activity approaching that of sorbinil (a highly effective AR inhibitor). Pyrazines aldo-keto reductase family 1 member B Homo sapiens