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35:
153:
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Batta, Ashok K.; Xu, Guorong; Honda, Akira; Miyazaki, Teruo; Salen, Gerald (2006). "Stigmasterol reduces plasma cholesterol levels and inhibits hepatic synthesis and intestinal absorption in the rat".
580:
Heinemann T, Kullak-Ublick GA, Pietruck B, von
Bergmann K (1991). "Mechanisms of action of plant sterols on inhibition of cholesterol absorption. Comparison of sitosterol and sitostanol".
107:(3β)-Stigmastan-3-ol; (3β,5α)-Stigmastan-3-ol; β-Sitostanol; Dihydrositosterin; Dihydrositosterol; Dihydro-β-sitosterol; Fucostanol; Spinastanol; 24α-Ethylcholestanol
553:
Heinemann T, Pietruck B, Kullak-Ublick G, von
Bergmann K (1988). "Comparison of sitosterol and sitostanol on inhibition of intestinal cholesterol absorption".
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from the diet. Animal studies suggest that it also inhibits biosynthesis of cholesterol in the liver.
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Sandqvist, Hakan; Bengtsson, Edvard (1931). "The empirical formula of sitosterol".
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139.4 to 139.8 °C (282.9 to 283.6 °F; 412.5 to 412.9 K)
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Except where otherwise noted, data are given for materials in their
152:
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34:
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Thomasson
Crompton, David William; Nickol, Brent B. (1985).
294:
622:
333:O1CC2(C)(CC3()2()CC4(C)3()CC4()(CC(CC)C(C)C)C)()C1
427:found in a variety of plant sources. Similar to
888:
490:Berichte der Deutschen Chemischen Gesellschaft B
256:
128:
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689:
629:. Cambridge University Press. p. 185.
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656:. Discovery Publishing Hous. p. 231.
435:, stigmastanol inhibits the absorption of
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234:
212:
582:European Journal of Clinical Pharmacology
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520:Metabolism: Clinical and Experimental
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442:Stigmastanol is the product of the
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94:)-1--9a,11a-dimethylhexadecahydro-1
24:
25:
913:
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33:
555:Agents and Actions. Supplements
401:(at 25 °C , 100 kPa).
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626:Biology of the Acanthocephala
532:10.1016/j.metabol.2005.08.024
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850:. You can help Knowledge by
7:
461:
98:-cyclopentaphenanthren-7-ol
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470:, a closely related sterol
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502:10.1002/cber.19310640849
653:Chemistry of Alkaloids
650:Paxena, P. B. (2007).
842:This article about a
58:Systematic IUPAC name
588:(Suppl 1): S59–63.
381: g·mol
51:5α-Stigmastan-3β-ol
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594:10.1007/BF01409411
405:Infobox references
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859:
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413:Chemical compound
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290:CompTox Dashboard
154:Interactive image
16:(Redirected from
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806:Stigmastadienone
776:δ-7-stigmasterol
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349:Chemical formula
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801:Stigmastadienol
766:δ-5-avenasterol
761:δ-7-avenasterol
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399:standard state
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745:Ergostadienol
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496:: 2167–2171.
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28:Stigmastanol
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897:Phytosterols
852:expanding it
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811:Stigmasterol
796:Stigmastenol
791:Stigmastanol
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771:β-Sitosterol
731:(Vitamin D2)
705:Phytosterols
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468:Stigmasterol
456:stigmasterol
448:β-sitosterol
441:
420:
417:Stigmastanol
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415:
194:ChEMBL252364
113:Identifiers
105:Other names
95:
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63:
786:Spinasterol
724:Campesterol
561:: 117–122.
437:cholesterol
425:phytosterol
342:Properties
232:100.001.345
174:CHEBI:89400
891:Categories
781:Momordenol
735:Ergostenol
729:Ergosterol
475:References
421:sitostanol
374:Molar mass
278:C2NJ9WO6O7
205:ChemSpider
141:3D model (
120:CAS Number
48:IUPAC name
18:Sitostanol
444:reduction
610:23279253
540:16483871
462:See also
450:and the
258:15559396
214:13078158
844:steroid
602:2044646
567:3265272
423:) is a
379:416.734
245:PubChem
130:83-45-4
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326:SMILES
185:ChEMBL
42:Names
846:is a
606:S2CID
165:ChEBI
143:JSmol
848:stub
658:ISBN
631:ISBN
598:PMID
563:PMID
536:PMID
431:and
269:UNII
90:,11a
754:C29
712:C28
590:doi
528:doi
498:doi
454:of
446:of
295:EPA
248:CID
86:,9b
82:,9a
74:,5a
70:,3b
66:,3a
893::
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293:(
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96:H
92:R
88:S
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72:R
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64:R
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