Title : Electrochemical and electron spin resonance studies of actinomycin D and other phenoxazones.

Pub. Date : 1985 Feb

PMID : 2983793






1 Functional Relationships(s)
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1 Substitution with electron-withdrawing groups such as NO2 (at C-7) and chloro (at C-1, C-2 and C-4)3 facilitated the reduction of the phenoxazone ring system to a free radical (i.e., half-wave potentials; 1, -0.815 V; 2, -0.920 V; 3, -0.135 V). Sodium Hypochlorite heterogeneous nuclear ribonucleoprotein C Homo sapiens