mats.v
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Okay common this is basic shit with big words
Testosterone, is a bioavailable, non ubiquitous hormone in all humans. It is inclined to be at significantly higher concentrations in the bloodstreams of biological males, compared to females. These significant differences in blood serum concentration of testosterone influence the majority of differences between men and women, such as virility and masculine features, aggression, strength, confidence, risk taking behavior etc, which are primary characteristics of testosterone..
In the early to mid twentieth century, Dutch pharmacologist Ernst Laqueur's research team (who isolated it from bull testes) and German chemists Adolf Butenandt and Leopold Ruzicka, developed the earliest forms of anabolic androgenic steroids via the development of an compound which was chemically identical to testosterone. When absorbed by the bloodstream, it mimics testosterone and increases its effects on the body…
Testosterone esters are a group of fatty acid chains which are attached to the testosterone compound.. esters influence the half life of a compound in the bloodstream..
testosterone is esterified in the 17β hydroxyl group with fatty acid esters of different aliphatic or other chain length which is a biologically inactive pro-drug.
The esterified testosterone in an oil vehicle is injected deeply into a muscle forming a local drug depot from which the testosterone ester is released at a slow rate determined by its physiochemical partitioning according to the testosterone ester’s hydrophobicity. Once the testosterone ester exits the depot and enters the extracellular fluids, it is rapidly hydrolyzed by ubiquitous non-specific esterases thereby releasing the testosterone into the general circulation.
Increased or decreased hydrophobicity, influences the length of bioavailability in the bloodstream. More hydrophobic esters like cypionate are significantly more active for longer periods of time (6-8 for cypionate) compared to propionate esters. And thus Cypionate a rate of physiochemical partitioning is slow and requires less often injections than propionate to maintain optimal desires serum concentration levels of the compound in the bloodstream
Testosterone, is a bioavailable, non ubiquitous hormone in all humans. It is inclined to be at significantly higher concentrations in the bloodstreams of biological males, compared to females. These significant differences in blood serum concentration of testosterone influence the majority of differences between men and women, such as virility and masculine features, aggression, strength, confidence, risk taking behavior etc, which are primary characteristics of testosterone..
In the early to mid twentieth century, Dutch pharmacologist Ernst Laqueur's research team (who isolated it from bull testes) and German chemists Adolf Butenandt and Leopold Ruzicka, developed the earliest forms of anabolic androgenic steroids via the development of an compound which was chemically identical to testosterone. When absorbed by the bloodstream, it mimics testosterone and increases its effects on the body…
Testosterone esters are a group of fatty acid chains which are attached to the testosterone compound.. esters influence the half life of a compound in the bloodstream..
testosterone is esterified in the 17β hydroxyl group with fatty acid esters of different aliphatic or other chain length which is a biologically inactive pro-drug.
The esterified testosterone in an oil vehicle is injected deeply into a muscle forming a local drug depot from which the testosterone ester is released at a slow rate determined by its physiochemical partitioning according to the testosterone ester’s hydrophobicity. Once the testosterone ester exits the depot and enters the extracellular fluids, it is rapidly hydrolyzed by ubiquitous non-specific esterases thereby releasing the testosterone into the general circulation.
Increased or decreased hydrophobicity, influences the length of bioavailability in the bloodstream. More hydrophobic esters like cypionate are significantly more active for longer periods of time (6-8 for cypionate) compared to propionate esters. And thus Cypionate a rate of physiochemical partitioning is slow and requires less often injections than propionate to maintain optimal desires serum concentration levels of the compound in the bloodstream
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