모든 사진(2)
About This Item
실험식(Hill 표기법):
C27H44O
CAS Number:
Molecular Weight:
384.64
MDL number:
UNSPSC 코드:
12352211
NACRES:
NA.25
추천 제품
설명
5α-cholesta-8,24-dien-3β-ol
분석
>99% (TLC)
양식
powder
포장
pkg of 1 × 1 mg (700068P-1mg)
pkg of 1 × 10 mg (700068P-10mg)
pkg of 1 × 5 mg (700068P-5mg)
제조업체/상표
Avanti Research™ - A Croda Brand
배송 상태
dry ice
저장 온도
−70°C
SMILES string
O[C@@H]1C[C@H]2[C@](CC1)(C3=C([C@H]4[C@@]([C@H](CC4)[C@@H](CCC=C(C)C)C)(CC3)C)CC2)C
InChI
1S/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h7,19-21,23-24,28H,6,8-17H2,1-5H3/t19-,20+,21+,23-,24+,26+,27-/m1/s1
InChI key
CGSJXLIKVBJVRY-XTGBIJOFSA-N
일반 설명
Zymosterol acts as an intermediate in the biosynthesis of cholesterol from lanosterol.
애플리케이션
- The ATPase activity of ABCA1 is increased by cholesterol in the presence of anionic lipids.: This study investigates the modulation of ATPase activity by cholesterol and anionic lipids, with a focus on the role of zymosterol in this biochemical pathway. The findings contribute to our understanding of lipid transport mechanisms and their implications in metabolic syndromes, emphasizing the potential therapeutic targets within these pathways (Sakata K et al., 2024).
- Effects of continuous intravenous infusion with propofol on intestinal metabolites in rats.: This research utilizes zymosterol as a biomarker to study the effects of propofol on intestinal metabolites, providing insights into the metabolic impacts of anesthesia on lipid biosynthesis pathways. The results are crucial for optimizing anesthesia protocols and understanding their systemic effects (Li J et al., 2024).
포장
5 mL Amber Glass Screw Cap Vial (700068P-10mg)
5 mL Amber Glass Screw Cap Vial (700068P-1mg)
5 mL Amber Glass Screw Cap Vial (700068P-5mg)
법적 정보
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
No data available
Flash Point (°C)
No data available
가장 최신 버전 중 하나를 선택하세요:
이미 열람한 고객
Sterol synthesis: a simple method for the isolation of zymosterol (5 alpha-cholesta-8, 24-dien-3 beta-ol) from yeast and spectral properties of zymosterol.
Taylor UF, et al.
Journal of Lipid Research, 22(1), 171-177 (1981)
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