Rhead, W. J.’s team published research in Bioinorganic Chemistry in 3 | CAS: 10510-54-0

Bioinorganic Chemistry published new progress about 10510-54-0. 10510-54-0 belongs to catalysis-chemistry, auxiliary class Other Aromatic Heterocyclic,Salt,Amine,Inhibitor,Inhibitor, name is 5,9-Diaminobenzo[a]phenoxazin-7-ium acetate, and the molecular formula is C18H15N3O3, COA of Formula: C18H15N3O3.

Rhead, W. J. published the artcileSelenium catalyzed reduction of methylene blue by thiols, COA of Formula: C18H15N3O3, the publication is Bioinorganic Chemistry (1974), 3(3), 225-42, database is CAplus and MEDLINE.

The reduction of methylene blue [61-73-4], of other reducible dyes, as well as of riboflavine [83-88-5], hemin [16009-13-5], and of vitamin B12a [13422-51-0] by thiols was catalyzed by ¦ÌM amounts of Se. The reduction of methylene blue was investigated in greater detail and exhibited a complicated dependence on the pH and the thiol concentration Alkylating agents, CN-, as well as Cd+2 or Hg+2 were inhibitory, whereas Cu2+ or Ag+ had stimulatory effects. Dithiols were more effective reducing agents than monothiols. The catalytic effects of Se in these reactions may parallel some of the functions of Se in vivo.

Bioinorganic Chemistry published new progress about 10510-54-0. 10510-54-0 belongs to catalysis-chemistry, auxiliary class Other Aromatic Heterocyclic,Salt,Amine,Inhibitor,Inhibitor, name is 5,9-Diaminobenzo[a]phenoxazin-7-ium acetate, and the molecular formula is C18H15N3O3, COA of Formula: C18H15N3O3.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia