JNJ-10181457 is a selective non-imidazole antagonist of the histamine H3 receptor, known to normalize acetylcholine neurotransmission. This compound also serves as a click chemistry reagent, featuring an alkyne group that enables it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions. Its properties make it valuable for insights into neurological signaling and the development of innovative chemical biology applications.
JNJ-10181457 is a selective non-imidazole antagonist of the histamine H3 receptor, known to normalize acetylcholine neurotransmission. This compound also serves as a click chemistry reagent, featuring an alkyne group that enables it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions. Its properties make it valuable for insights into neurological signaling and the development of innovative chemical biology applications.
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