Campestanol

• CAT Number: I023993
• CAS Number: 474-60-2
• Molecular Formula: C28H50O
• Molecular Weight: 402.71
• Purity: 98%
• Solubility: Soluble in DMSO
• Storage: Store at -20°C
• IUPAC Name: (3S,5S,8R,9S,10S,13R,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
• InChI: InChI=1S/C28H50O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h18-26,29H,7-17H2,1-6H3/t19-,20-,21+,22+,23+,24-,25+,26+,27+,28-/m1/s1
• InChIKey: ARYTXMNEANMLMU-ATEDBJNTSA-N
• SMILES: O[C@H]1CC[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@H]([C@@H](CC[C@@H](C)C(C)C)C)CC[C@@]4([H])[C@]3([H])CC[C@@]2([H])C1

Campestanol（Cat No.:I023993） is a naturally occurring plant sterol that belongs to the group of phytosterols. It is commonly found in various plant sources, including vegetables, fruits, grains, and nuts. Campestanol shares structural similarities with cholesterol but is derived from plant sources instead of animals. It is known for its potential health benefits, such as its cholesterol-lowering properties and its role in maintaining cardiovascular health. Campestanol is often consumed as part of a balanced diet and is considered a valuable component of plant-based nutrition.

Reference

1: Connor WE, Lin DS, Pappu AS, Frohlich J, Gerhard G. Dietary sitostanol and campestanol: accumulation in the blood of humans with sitosterolemia and xanthomatosis and in rat tissues. Lipids. 2005 Sep;40(9):919-23. PubMed PMID: 16331855.
2: Salen G, Xu G, Tint GS, Batta AK, Shefer S. Hyperabsorption and retention of campestanol in a sitosterolemic homozygote: comparison with her mother and three control subjects. J Lipid Res. 2000 Nov;41(11):1883-9. PubMed PMID: 11060358.
3: Xu G, Salen G, Tint GS, Batta AK, Shefer S. Campestanol (24-methyl-5alpha-cholestan-3beta-ol) absorption and distribution in New Zealand White rabbits: effect of dietary sitostanol. Metabolism. 1999 Mar;48(3):363-8. PubMed PMID: 10094114.
4: Kircher HW, Rosenstein FU. Purification of campesterol and preparation of 7-dehydrocampesterol, 7-campestenol and campestanol. Lipids. 1974 May;9(5):333-7. PubMed PMID: 4857275.