7.7
[]. Bell SG, et al. A cytochrome P45 class I electron transfer system from Novosphingobium aromaticivorans. Appl Microbiol Biotechnol. 2 Mar;86():63-75.
[2]. C Tetreau, et al. Conformational relaxation in hemoproteins: the cytochrome P-45cam case. Biochemistry. 2 Nov 2;39(46):429-3.
[3]. E Mariani, et al. (+/-)--(Adamantan-2-yl)-2-propanamine and other amines derived from 2-adamantanone. Farmaco Sci. 98 May;35(5):43-4.
[4]. Hassen Jaafar, et al. Tuning the conversion of cyclohexane into cyclohexanol/one by molecular dioxygen, protons and reducing agents at a single non-porphyrinic iron centre and chemical versatility of the tris(2-pyridylmethyl)amine TPAFe(II)Cl2 complex in mild oxidation chemistry. Dalton Trans. 2 Jan 7;4():92-6.
[5]. I E Kovalev, et al. Effect of adamantanone derivative possessing anti-HIV properties on the redox processes in the cytochrome P-45 system. Dokl Biochem Biophys. 2 May-Jun:378:2-3.
H32-H35-H39-H335
P26-P264-P27-P27-P28-P32+P352-P34+P34-P35+P35+P338-P33-P362+P364-P43+P233-P45-P5
GHS7