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Substitution at R3 with a halogen or alkoxy group (74f–74i) triggered a slight boost in mobile potency While using the halide analogs (74g–h) demonstrating optimum the potency from the group. Even further optimization brought about the discovery of 74i–j, with 74k as probably the most active compound during the sequence (pIC50 = 6.seventy sev

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The existing review not just updates recent developments in new reactions with the synthesis of indazole derivatives and their software in the medicinal subject but also encourages medicinal chemists to even further discover novel indazoles as likely drug candidates for useful therapeutics.Owing to the importance of the indole for a scaffold in pur

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