Metabolism of stanozolol: Chemical synthesis and.
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metabolites of stanozolol dosage
Serum zinc concentrations and urinary zinc excretion rate. a Significantly different from week 0, P <0.05; b significantly different from week 0, P <0.01; c significantly different from placebo, P <0.05; and d significantly different from placebo, P <0.01.
Urine pH and urine flow in subjects using ZMA (grey) or placebo (white). a Significantly different from week 0, P <0.05; c significantly different from placebo, P <0.05; and d significantly different from placebo, P <0.01.
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An understanding of metabolism is pivotal to comprehending the phenotypic behavior of all living organisms (including humans) where metabolism is integral to health and proper functioning. Metabolites are the intermediate products of metabolic reactions catalyzed by various enzymes that naturally occur within cells. This term is usually used to describe small molecules, although broader application is often practiced.
Primary metabolites are synthesized by the cell because they are indispensable for their growth. Significant representatives are amino acids, alcohols, vitamins (B2 and B12), polyols, organic acids, as well as nucleotides (e.g. inosine-5'-monophosphate and guanosine-5'-monophosphate).
Secondary metabolites are compounds produced by an organism that are not required for primary metabolic processes, although they can have important ecologic and other functions. They include drugs, fragrances, flavor, dye, pigments, pesticides and food additives with applications in agriculture, industry and pharmaceuticals.
Arachidonic acid is a metabolite of prostaglandin and both molecules contain similar functional groups, have similar physical properties and demonstrate nearly identical formulas. In addition, both compounds are linked by a defined series of enzyme-catalyzed reactions with a logical progression of chemical change. Inosine-5'-monophosphate is a metabolite that arises by condensing two or more intermediates (namely phosphoribosyl-pyrophosphate and glutamine) with a one way directionality based on the principles of free energy exchange.
The key to understanding anabolic steroid detection times lies in the ability to learn about and understand how drug testing for anabolic steroids and performance enhancing drugs works, and what exactly are the factors involved in affecting anabolic steroid detection times. Drug testing for anabolic steroids and related performance enhancing drugs is one of the most misunderstood topics and concepts by both the average individual as well as those athletes, bodybuilders, and individuals who actually use anabolic steroids. There are in fact a few popular misconceptions in regards to anabolic steroid testing .
The very expensive procedures (and equipment) for the purpose of anabolic steroid detection involves the use of gas chromatography-mass spectrometry, and even liquid chromatography-mass spectrometry     . These are all extremely expensive procedures and pieces of equipment, costing millions of dollars in order to test perhaps only a handful of individuals.
This is evidenced in history during the Olympics, where East Germany ran a state-sponsored program known as State Plan Research Theme 14.25, which as a program designed to circumvent the IOC testing procedures and have all of their Olympic athletes (both knowingly and unknowingly) utilizing anabolic steroids in an effort to undetectably gain an advantage over other competitors  . The East German government implemented this program and ran it for over 20 years, and involved the use of undetectable (at the time) anabolic steroids, due to their relatively new development and unknown status.
Steroid detection times can be influenced by many different factors, mostly involving the different metabolic pathways and excretion methods. Anabolic steroid detection times can be influenced by the type of anabolic steroid used, the specific properties of that anabolic steroid, the dose, the duration of use, and route of administration (oral or injectable).
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