Okay let’s say I inject 400mg EW of a compound like CYP with its 12dy half life. So on day 1 I have 400mg of Test with 8 carbons attached to it. This test is essentially inactive until some of those carbons start falling off and the test is released. This happens at a rate roughly equal to 5.5% per day (resulting in 50% over 12dy). Once the test is freed from the carbons the hormone has a very short active life in my body, its either bound to SHBG, amortized, bound to receptors or metabolized by my liver. My point is I’m never really “on 400mg EW” its more like I’m on up to 50mg ED (cumulative impact of successive 400mg weeks) for some time. I think the body produces something like 8mg to 12mg ED, thus it’s conceivable that you could use this information to help in planning the start of PCT.

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