| Name | methemoglobin |
|---|---|
| Synonyms | Abnormal hemoglobin; G gamma globin; Gamma 2 globin; HBG 2; HBG2; Hb F Ggamma; Hemoglobin gamma G; Hemoglobin gamma 2 chain… |
| Name | diphenylamine |
|---|---|
| CAS |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 8956097 | Vick JA, Von Bredow JD: Effectiveness of intramuscularly administered antidotes on methemoglobin formation and survival. J Appl Toxicol. 1996 Nov-Dec;16(6):509-16. |
4(0,0,0,4) | Details |
| 598785 | Nomura A: [Studies of sulfhemoglobin formation by various drugs (3) (author's transl)]. Nippon Yakurigaku Zasshi. 1977 Oct;73(7):793-802. Sulfhemoglobin (SHb) and methemoglobin (MHb) formations by various compounds were examined by single and three consecutive intraperitoneal administrations to mice. With a single administration, methemoglobinemia was induced by diphenylamine (DPA), 1-naphthylamine (NA), phenylnaphthylamine (PNA), N-(1-naphthyl) (N1) and N-(1'-naphthyl)- (IG240), and was not observed with phenylanthranilic acid (PAA), N-benzoyl-N'-phenyl-2, 6-diaminobenzoic acid (BPAA), flufenamic acid (FA), mefenamic acid (MFA), N-(2-6-dichlorophenyl) (CPAA), N-(2', 6'-dichlorophenyl)- (CPPA), nine derivatives of N1 and two derivatives of IG240. |
1(0,0,0,1) | Details |
| 6743655 | Sullivan SG, Stern A: Membrane protein changes induced by tert-butyl hydroperoxide in red blood cells. Biochim Biophys Acta. 1984 Jul 25;774(2):215-20. Crosslinking was partially prevented by metabolism of t-butyl hydroperoxide by the hexose monophosphate shunt except in methemoglobin-containing red cells where reaction with methemoglobin accounted for most of the consumption of t-butyl hydroperoxide. Butylated hydroxytoluene, diphenylamine and compounds that inhibit t-butyl hydroperoxide-induced red cell membrane lipid peroxidation, had no effect on t-butyl hydroperoxide-induced membrane protein changes. |
1(0,0,0,1) | Details |
| 1312811 | Akaike T, Sato K, Ijiri S, Miyamoto Y, Kohno M, Ando M, Maeda H: Bactericidal activity of alkyl peroxyl radicals generated by heme-iron-catalyzed decomposition of organic peroxides. Arch Biochem Biophys. 1992 Apr;294(1):55-63. In addition, bactericidal activity was completely inhibited by the addition of the spin trap DMPO, as well as of other various radical scavengers and into the peroxide-heme iron system, but this effect was not observed with superoxide dismutase, diphenylamine, or butylated hydroxyltoluene. The major cytotoxic radical species generated in the mixtures of various peroxides and heme iron, especially methemoglobin, metmyoglobin, or hemin, was the alkyl peroxyl radical (ROO.). |
1(0,0,0,1) | Details |