8556. β-Sitosterol

Nomenclature

CAS number: 83-46-5
(3β)-Stigmast-5-en-3-ol; 22:23-dihydrostigmasterol; α-dihydrofucosterol; Δ5-stigmasten-3β-ol; 24β-ethyl-Δ5-cholesten-3β-ol; α-phytosterol; cinchol; cupreol; rhamnol; quebrachol; sitosterin; Harzol (Hoyer); Prostasal (TAD); Sito-Lande (Delalande).
C29H50O; mol wt 414.71.
C 83.99%, H 12.15%, O 3.86%.

Description and references

Common sterol in plants. Isoln from wheat germ oil, corn oil: Anderson et al., J. Am. Chem. Soc. 48, 2987 (1926); from rye germ oil: Gloyer, Schuette, ibid. 61, 1901 (1939); from cottonseed oil: Wallis, Chakravorty, J. Org. Chem. 2, 335 (1937); from tall oil: Sandqvist, Bengtsson, Ber. 64, 2167 (1931). Also occurs in soy and calabar beans, in rice embryos: Tanaka, J. Biochem. 17, 483 (1933); in cascara, cinchona bark and cinchona wax: Dirscherl, Z. Physiol. Chem. 235, 1 (1935). Prepn from tall oil: G. I. Fujimoto, A. E. Jacobson, J. Org. Chem. 29, 3377 (1964). Identity with 22:23-dihydrostigmasterol: W. Dirscherl, H. Nahm, Ann. 555, 57 (1944). Identity with cinchol: eidem, Ann. 558, 231 (1947). Structure: Bernstein, Wallis, J. Org. Chem. 2, 341 (1937); Bergmann, Low, ibid. 12, 67 (1947); Shoppee, J. Chem. Soc. 1948, 1032. Stereospecific synthesis: W. Sucrow, M. Slopianka, Ber. 108, 3721 (1975). Clinical efficacy in treatment of type II hyperlipoproteinemia: R. S. Lees, A. M. Lees, in Lipoprotein Metabolism, H. Greten, Ed. (Springer-Verlag, New York, 1976) pp 119-124; P. Oster et al., ibid. pp 125-130. Studies on inhibition of cholesterol absorption: S. M. Grundy, H. Y. I. Mok, ibid. pp 112-118; I. Ikeda, M. Sugano, Biochim. Biophys. Acta 732, 651 (1983). Inhibition of induced carcinogenesis: N. D. Nigro et al., J. Natl. Cancer Inst. 69, 103 (1982). Clinical trial in treatment of prostatic adenoma: H.-P. Szutrely, Med. Klin. 77, 520 (1982). Book: Monographs on Atherosclerosis Vol. 10, T. B. Clarkson et al., Eds. entitled “Sitosterol” by O. J. Pollak, D. Kritchevsky (Karger, Basel, 1981) 219 pp.

Chemical structure

Properties

Plates from alcohol, mp 140°. [α]D25 -37° (c = 2 in chloroform).

Derivative

Acetate.
C31H52O2; mol wt 456.74.
C 81.52%, H 11.48%, O 7.01%.

Properties

mp 127-128°. [α]D25 -41° (c = 2 in chloroform).

Therapeutic Category

Antilipemic. Treatment of prostatic adenoma.

Keywords

Antilipemic