{"id":35211,"date":"2026-09-28T21:14:58","date_gmt":"2026-09-28T21:14:58","guid":{"rendered":"https:\/\/izchem.com\/?post_type=product&p=35211"},"modified":"2026-09-28T21:15:15","modified_gmt":"2026-09-28T21:15:15","slug":"am-2232","status":"publish","type":"product","link":"https:\/\/izchem.com\/fr\/am-2232\/","title":{"rendered":"AM 2232"},"content":{"rendered":"

AM-2232<\/strong> Il s'agit d'un cannabino\u00efde de synth\u00e8se utilis\u00e9 en recherche, appartenant \u00e0 la famille des aminoalkylindoles, agonistes des r\u00e9cepteurs cannabino\u00efdes. Gr\u00e2ce \u00e0 sa structure mol\u00e9culaire bien caract\u00e9ris\u00e9e et \u00e0 son profil de liaison aux r\u00e9cepteurs cannabino\u00efdes, il est largement utilis\u00e9 comme \u00e9talon de r\u00e9f\u00e9rence analytique en toxicologie m\u00e9dico-l\u00e9gale, en chimie m\u00e9dicinale, en recherche pharmaceutique et en chimie analytique.<\/p>\n

L'AM-2232 constitue un mat\u00e9riau de r\u00e9f\u00e9rence important pour les chercheurs qui \u00e9tudient les cannabino\u00efdes synth\u00e9tiques, les m\u00e9thodes de d\u00e9tection analytique et la pharmacologie des r\u00e9cepteurs cannabino\u00efdes.<\/p>\n

Qu'est-ce que l'AM-2232\u00a0?<\/h2>\n

L'AM-2232 est un cannabino\u00efde de synth\u00e8se d\u00e9velopp\u00e9 en laboratoire, devenu pr\u00e9cieux pour la recherche sur les r\u00e9cepteurs cannabino\u00efdes et les analyses m\u00e9dico-l\u00e9gales. Sa structure aminoalkylindole et sa substitution naphtoyle le rendent utile pour l'\u00e9tude de la chimie des cannabino\u00efdes de synth\u00e8se, leur identification analytique et l'interaction avec les r\u00e9cepteurs dans des conditions de laboratoire contr\u00f4l\u00e9es.<\/p>\n

Les chercheurs utilisent couramment l'AM-2232 comme \u00e9talon de r\u00e9f\u00e9rence analytique certifi\u00e9 pour d\u00e9velopper et valider des m\u00e9thodes de d\u00e9tection en laboratoire.<\/p>\n

La Structure chimique et les Propri\u00e9t\u00e9s<\/h2>\n

Les principales caract\u00e9ristiques chimiques comprennent\u00a0:<\/p>\n

    \n
  • squelette aminoalkylindole<\/li>\n
  • structure de l'indole naphtoyle<\/li>\n
  • cha\u00eene lat\u00e9rale cyanobutyle<\/li>\n
  • Mat\u00e9riau de r\u00e9f\u00e9rence analytique de haute puret\u00e9<\/li>\n
  • Stable dans les conditions de stockage recommand\u00e9es en laboratoire<\/li>\n<\/ul>\n

    Sa conception mol\u00e9culaire permet des \u00e9tudes comparatives impliquant des analogues de cannabino\u00efdes synth\u00e9tiques et des recherches sur la liaison aux r\u00e9cepteurs.<\/p>\n

    Les Applications Scientifiques<\/h2>\n

    L'AM-2232 est couramment utilis\u00e9 dans\u00a0:<\/p>\n

      \n
    • Recherche sur les r\u00e9cepteurs cannabino\u00efdes<\/li>\n
    • Chimie m\u00e9dicinale<\/li>\n
    • d\u00e9veloppement pharmaceutique<\/li>\n
    • Chimie analytique<\/li>\n
    • Toxicologie m\u00e9dico-l\u00e9gale<\/li>\n
    • enqu\u00eates sur les cannabino\u00efdes de synth\u00e8se<\/li>\n
    • Recherche sur les nouvelles substances psychoactives (NPS)<\/li>\n
    • \u00e9tudes sur les relations structure-activit\u00e9 (RSA)<\/li>\n<\/ul>\n

      Ces applications contribuent \u00e0 une meilleure identification analytique et \u00e0 une meilleure compr\u00e9hension scientifique des ligands des r\u00e9cepteurs cannabino\u00efdes.<\/p>\n

      Applications Analytiques De<\/h2>\n

      Les laboratoires professionnels utilisent fr\u00e9quemment l'AM-2232 pour\u00a0:<\/p>\n

        \n
      • Liquid Chromatography\u2013Mass Spectrometry (LC-MS\/MS)<\/li>\n
      • Gas Chromatography\u2013Mass Spectrometry (GC-MS)<\/li>\n
      • Chromatographie liquide haute performance (HPLC)<\/li>\n
      • Spectrom\u00e9trie de Masse haute R\u00e9solution (HRMS)<\/li>\n
      • \u00c9talonnage de r\u00e9f\u00e9rence<\/li>\n
      • Validation de la m\u00e9thode<\/li>\n
      • \u00e9valuation de la puret\u00e9 chimique<\/li>\n
      • Assurance qualit\u00e9 de laboratoire<\/li>\n<\/ul>\n

        Ces m\u00e9thodes analytiques permettent une caract\u00e9risation et une identification fiables des compos\u00e9s cannabino\u00efdes de synth\u00e8se.<\/p>\n

        Pourquoi les chercheurs \u00e9tudient-ils l'AM-2232 ?<\/h2>\n

        Les int\u00e9r\u00eats scientifiques comprennent\u00a0:<\/p>\n

          \n
        • \u00c9tudes sur les r\u00e9cepteurs cannabino\u00efdes<\/li>\n
        • Profilage des cannabino\u00efdes synth\u00e9tiques<\/li>\n
        • Recherche en chimie m\u00e9dicinale<\/li>\n
        • Caract\u00e9risation des compos\u00e9s pharmaceutiques<\/li>\n
        • D\u00e9veloppement de m\u00e9thodes analytiques<\/li>\n
        • Identification m\u00e9dico-l\u00e9gale<\/li>\n
        • Surveillance \u00e9mergente des NPS<\/li>\n
        • D\u00e9veloppement de normes de r\u00e9f\u00e9rence<\/li>\n<\/ul>\n

          Ses caract\u00e9ristiques structurelles uniques rendent l'AM-2232 pr\u00e9cieux pour la recherche analytique et comparative sur les cannabino\u00efdes.<\/p>\n

          Recherche Li\u00e9e \u00c0 Des Compos\u00e9s<\/h2>\n

          Les chercheurs comparent fr\u00e9quemment l'AM-2232 avec\u00a0:<\/p>\n

            \n
          • AM-2233<\/li>\n
          • AM-694<\/li>\n
          • AM-1235<\/li>\n
          • JWH-018<\/li>\n
          • THJ-2201<\/li>\n
          • FUBIMINA<\/li>\n
          • O-774<\/li>\n
          • O-1812<\/li>\n<\/ul>\n

            Les \u00e9tudes comparatives permettent de mieux comprendre la diversit\u00e9 structurelle et la diff\u00e9renciation analytique des cannabino\u00efdes de synth\u00e8se.<\/p>\n

            Applications de recherche<\/h2>\n

            Les applications potentielles en laboratoire comprennent\u00a0:<\/p>\n

              \n
            • Recherche pharmaceutique<\/li>\n
            • Chimie m\u00e9dicinale<\/li>\n
            • Chimie analytique<\/li>\n
            • Toxicologie m\u00e9dico-l\u00e9gale<\/li>\n
            • \u00c9tudes sur les r\u00e9cepteurs cannabino\u00efdes<\/li>\n
            • Recherche universitaire<\/li>\n
            • Caract\u00e9risation chimique<\/li>\n
            • D\u00e9veloppement de la norme de r\u00e9f\u00e9rence<\/li>\n<\/ul>\n

              De stockage et de Manutention<\/h2>\n

              Pour optimiser le laboratoire de la stabilit\u00e9:<\/p>\n

                \n
              • Magasin \u00e9tanche \u00e0 l'air dans les r\u00e9cipients de laboratoire.<\/li>\n
              • \u00c0 prot\u00e9ger de l'humidit\u00e9 et de la lumi\u00e8re directe du soleil.<\/li>\n
              • Maintenir recommand\u00e9 de laboratoire temp\u00e9ratures de stockage.<\/li>\n
              • Manipuler en utilisant un \u00e9quipement de protection individuelle (EPI) de laboratoire appropri\u00e9.<\/li>\n
              • Suivez laboratoire institutionnel proc\u00e9dures de s\u00e9curit\u00e9.<\/li>\n
              • R\u00e9serv\u00e9 au personnel de laboratoire qualifi\u00e9.<\/li>\n<\/ul>\n

                Foire aux questions<\/h2>\n

                Qu'est-ce que l'AM-2232\u00a0?<\/h3>\n

                L'AM-2232 est un cannabino\u00efde synth\u00e9tique aminoalkylindole utilis\u00e9 comme \u00e9talon de r\u00e9f\u00e9rence analytique en toxicologie m\u00e9dico-l\u00e9gale, en recherche sur les r\u00e9cepteurs cannabino\u00efdes, en chimie m\u00e9dicinale et en sciences pharmaceutiques.<\/p>\n

                Quels sont les domaines de recherche qui utilisent couramment l'AM-2232\u00a0?<\/h3>\n

                Il est largement utilis\u00e9 dans la recherche sur les r\u00e9cepteurs cannabino\u00efdes, la toxicologie m\u00e9dico-l\u00e9gale, la chimie analytique, la chimie m\u00e9dicinale, le d\u00e9veloppement pharmaceutique et les enqu\u00eates sur les cannabino\u00efdes synth\u00e9tiques.<\/p>\n

                Quelles m\u00e9thodes analytiques conviennent \u00e0 l'AM-2232\u00a0?<\/h3>\n

                Les chercheurs utilisent couramment les techniques LC-MS\/MS, GC-MS, HPLC et HRMS pour l'identification des compos\u00e9s, la validation analytique, l'\u00e9talonnage et l'assurance qualit\u00e9.<\/p>\n

                Pourquoi l'AM-2232 est-il important dans la recherche en laboratoire\u00a0?<\/h3>\n

                Sa structure mol\u00e9culaire bien caract\u00e9ris\u00e9e la rend pr\u00e9cieuse pour les recherches sur les cannabino\u00efdes synth\u00e9tiques, le d\u00e9veloppement de m\u00e9thodes analytiques, l'identification m\u00e9dico-l\u00e9gale et les \u00e9tudes de relations structure-activit\u00e9.<\/p>\n

                Le compos\u00e9 AM-2232 est-il destin\u00e9 uniquement \u00e0 la recherche en laboratoire\u00a0?<\/h3>\n

                Oui. L'AM-2232 est fourni exclusivement \u00e0 des fins de recherche scientifique, de laboratoire, d'analyse et d'enseignement.<\/p>\n

                Avertissement<\/h2>\n

                L'AM-2232 est exclusivement destin\u00e9 \u00e0 la recherche en laboratoire, scientifique, analytique et p\u00e9dagogique. Ce produit est pas<\/strong> Ce produit est destin\u00e9 \u00e0 la consommation humaine, aux traitements m\u00e9dicaux, aux applications v\u00e9t\u00e9rinaires, \u00e0 un usage th\u00e9rapeutique ou \u00e0 des fins de diagnostic. Il incombe aux utilisateurs de se conformer \u00e0 toutes les lois, r\u00e9glementations institutionnelles et exigences de s\u00e9curit\u00e9 en laboratoire applicables.<\/p>","protected":false},"excerpt":{"rendered":"

                  \n
                • Nom Du Produit:<\/strong>AM-2232<\/li>\n
                • Noms Alternatifs: <\/strong>AM2232, 1-(4-Cyanobutyl)-3-(naphtal\u00e9n-1-oyl)indole<\/li>\n
                • Classe Chimique: <\/strong>Synthetic Cannabinoid \u2022 Aminoalkylindole \u2022 Cannabinoid Receptor Ligand<\/li>\n
                • Cat\u00e9gorie de recherche\u00a0: <\/strong>Produits chimiques de recherche sur les cannabino\u00efdes<\/li>\n<\/ul>","protected":false},"featured_media":35217,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_uag_custom_page_level_css":"","site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center 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Name:AM-2232 Alternative Names: AM2232, 1-(4-Cyanobutyl)-3-(naphthalen-1-oyl)indole Chemical Class: Synthetic Cannabinoid \u2022 Aminoalkylindole \u2022 Cannabinoid Receptor Ligand Research Category: Cannabinoid Research 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