Uncoupling of photophosphorylation by 2-alkylbenzimidazoles was written by Trebst, A.;Pistorius, E.;Buechel, K. H.. And the article was included in Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, Biochemie, Biophysik, Biologie in 1966.Recommanded Product: 13060-24-7 This article mentions the following:
2-Alkylbenzimidazoles exhibited little or no inhibition of the Hill reaction in isolated spinach chloroplasts, but were effective uncouplers of photophosphorylation. 2-Alkylbenzimidazoles, with side chains, of from 8 to 14 C atoms, uncoupled noncyclic and cyclic photophosphorylation at <10-5M. 2-Decylbenzimidazole was the most potent uncoupler. 2-Undecylbenzimidazole stimulated the Hill reaction in the absence of the phosphorylation system and shifted the pH optimum to a lower value. 25 references. In the experiment, the researchers used many compounds, for example, 2-Octylbenzimidazole (cas: 13060-24-7Recommanded Product: 13060-24-7).
2-Octylbenzimidazole (cas: 13060-24-7) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Imidazole based anticancer drug find applications in cancer chemotherapy. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC).Recommanded Product: 13060-24-7
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem