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Stanozolol (also known as winstrol) is a 17-alpha-alkylated derivative of dihydrotestosterone (DHT) with low androgenic qualities yet highly anabolic.

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It was first developed in 1962 by American global pharmaceutical company Sterling-Winthrop Laboratories to increase lymphocyte count and CD8+ cell numbers, but to decrease CD4+ and CD3+ in postmenopausal women using it for osteoporosis.

This effect would plausibly be useful for treatment of autoimmune disorders. Winstrol is useful in treatment of hereditary angioedema. It also influences some immunological processes.  Stanozolol tablets have a short life time (about 9 hours) as compared against injectable stanozolol.

The injectable version of stanozolol differs from other injectable anabolic steroids in being an aqueous suspension of fine particles of steroid, instead of being an oil solution of an esterified compound. For this reason, it has unusual pharmacokinetics which do not follow the classic half-life pattern. Instead, there is a sustained effect which slowly tapers.

Although stanozolol is a DHT based compound, its activity is much milder than this androgen in nature.

As a result stanozolol does not cause water retention. On the contrary, it possess a diuretic effect. So, instead of bulk look winstrol produces a lean, quality look without excess subcutaneous water retention.

This happens due to winstrol`s possibility to dry out the joint fluid, which can lead to joint pain and damages. Also both stanozolol forms: tablets and injections have been noted to provoke adverse changes in cholesterol levels. Hence, monitoring of the lipid profile of the body (blood works) during cycle is advisable.