To PJ: Yes. Carcinogens may be chemical, organic, or viral in origin, but they all have this common feature of an ability to bind to vital parts of the ox-phos pathway, thereby preventing ubiquinone from carrying out its function. When you remove them ( by creating a peroxide free radical, just as ubiquinone creates a free radical as part of its delivery process) this initiates a chain reaction which works throughout the system and eliminates cancer cells from every part of the body, not just the primary site. That is how it solves the problem of metastasis. I can send you the biochemistry if you let me have your address.
Ubiquinone itself cannot do this, because its electronegativitity is weakened by its substituent methyl groups and its isoprenoid tail (these 10 isoprenoid units in humans are why it is sometimes referred to as CoQ10, as you probably know). Para benzoquinone does not have these methyl groups around the ring, nor any isoprenoid units (Ubiquinone needs them to maintain its position in the plasma membrane), which gives it a much greater RP value.
Are you beginning to understand the mechanism now? It a bit of a digression, but will help later when I deal with the effects of electric fields on this process inter alia.
Ubiquinone itself cannot do this, because its electronegativitity is weakened by its substituent methyl groups and its isoprenoid tail (these 10 isoprenoid units in humans are why it is sometimes referred to as CoQ10, as you probably know). Para benzoquinone does not have these methyl groups around the ring, nor any isoprenoid units (Ubiquinone needs them to maintain its position in the plasma membrane), which gives it a much greater RP value.
Are you beginning to understand the mechanism now? It a bit of a digression, but will help later when I deal with the effects of electric fields on this process inter alia.