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Phytosteroid
 (

Phytosteroids, also known as plant steroids, are that are found in .

(2013). 9789401730785, Springer Science & Business Media. .
Examples include , , , and , as well as like β-sitosterol.


Industrial use
pharmaceuticals that are identical or similar to human are very widely used in medicine. However, the four-ring structure of a steroid is quite expensive to replicate using direct synthetic methods.

In 1938–1940, American chemist Russell Earl Marker developed the process known as Marker degradation, which converts from Mexican yams into 16-dehydropregnenolone acetate, which has a four-ring structure and can be used to synthesize commonly used steroid hormones. Marker's process reduced the price of from $80/gram in early 1944 to $2/gram in 1951.

Also in 1940, American chemist Percy Lavon Julian discovered a process to convert a much more abundant phytosteroid -- from -- into progesterone. Stigmasterol is a byproduct of soybean oil refinement. His process was improved by Padmanabhan Sundararaman and in 1977, just as stocks of wild Mexican yam became depleted. Soy stigmasterol soon replaced yam diosgenin as the main starting material for hormone production globally.

(2026). 9780822346050, Duke University. .

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