Hojo, Yasuji published the artcileSpecific ability of sulfur-ligands to remove mercury-203-labeled organomercury from hemoglobin in comparison with nitrogen-ligands, SDS of cas: 10517-44-9, the publication is Radioisotopes (1975), 24(10), 684-8, database is CAplus.
Organomercurials (chloromerodrin [62-37-3], methylmercuric chloride [115-09-3], ethylmercuric chloride [107-27-7] and phenylmercuric acetate [62-38-4]) bound to sulfhydryl groups of Hb were removed by chelating agents including sulfur-ligands (penicillamine [52-67-5], glutathione [70-18-8]) and nitrogen-ligands (EDTA [60-00-4], glycine [56-40-6], polyethylenediamines). The effect of sulfur-ligands was higher and more sp. than that of nitrogen-ligands. A linear correlation was observed between the extent of organomercurial removal and the stability constant (log K1) of the organomercury complex with sulfur- and nitrogen-ligands. At a fixed value of log K1, sulfur-ligands were more effective than nitrogen-ligands. With the exception of chloromeredin, a linear correlation was also observed between the average percentage of removal and the Taft’s polar substituent constant for the organic moiety of the metal. The average removal percentage by sulfur-ligands increased in the order: ethylmercury > methylmercury > phenylmercury, whereas that by nitrogen-ligands was similar.
Radioisotopes published new progress about 10517-44-9. 10517-44-9 belongs to catalysis-chemistry, auxiliary class Salt,Amine,Aliphatic hydrocarbon chain, name is Propane-1,3-diamine dihydrochloride, and the molecular formula is C3H12Cl2N2, SDS of cas: 10517-44-9.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia