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6-fluoro-2-[2-hydroxy-3-(2-methyl-cyclohexyloxy)-phenyl]-1H-indole-5-carboxamidine is a synthetic small molecule belonging to the class of organic compounds known as 2‑phenylindoles[1][2][3]. It features an indole core substituted with a phenolic group and a carboxamidine moiety. The compound has been studied experimentally and is not approved for clinical use. Its mechanism of action involves inhibition of serine proteases, including coagulation factor X (FA10), plasminogen (PLMN), prothrombin (THRB), tissue-type plasminogen activator (TPA), trypsin, and urokinase-type plasminogen activator (UROK)[1]. These targets suggest potential anticoagulant or antifibrinolytic activity, but there are no indications that it has advanced beyond experimental research.
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