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Benzyloxybenzaldehyde analogues as novel adenylyl cyclase activators

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BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 11, 期 15, 页码 1971-1974

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0960-894X(01)00353-5

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Several benzyloxybenzaldehyde analogues were prepared and found to have significant inhibitory activity toward neutrophil superoxide formation. Consequently, these compounds were evaluated for cAMP-elevating capability. Among them, benzyloxybenzaldehyde (7), exhibiting activity equivalent to forskolin, was determined as an adenylyl cyclase activator since it elevates cAMP levels by activation of adenylyl cyclase but not by inhibition of phosphodiesterase. Having a chemical structure very different from known adenylyl cyclase activators, compound 7 is recommended by us for use as a new lead compound in the future development of adenylyl cyclase activators. (C) 2001 Elsevier Science Ltd. All rights reserved.

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