推荐产品
描述
1-heptadecanoyl-2-hydroxy-sn-glycero-3-phosphocholine
化驗
>99% (LPC; may contain up to 10% of the 2-LPC isomer, TLC)
形狀
powder
包裝
pkg of 1 × 200 mg (855676P-200mg)
pkg of 1 × 25 mg (855676P-25mg)
製造商/商標名
Avanti Research™ - A Croda Brand
運輸包裝
dry ice
儲存溫度
−20°C
SMILES 字串
O[C@](COP([O-])(OCC[N+](C)(C)C)=O)([H])COC(CCCCCCCCCCCCCCCC)=O
InChI
1S/C25H52NO7P/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-25(28)31-22-24(27)23-33-34(29,30)32-21-20-26(2,3)4/h24,27H,5-23H2,1-4H3/t24-/m1/s1
InChI 密鑰
SRRQPVVYXBTRQK-XMMPIXPASA-N
應用
- Serum lipids profiling perturbances in patients with ischemic heart disease and ischemic cardiomyopathy.: This study examines alterations in serum lipid profiles among patients with ischemic conditions, potentially highlighting roles of specific lipid molecules like 17:0 Lyso PC in the pathology of these diseases (Yang et al., 2020).
包裝
5 mL 棕色玻璃螺纹口样品瓶 (855676P-25mg)
5 mL 棕色玻璃螺纹口样品瓶(855676P-200mg)
法律資訊
Avanti Research is a trademark of Avanti Polar Lipids, LLC
也與該產品經常一起購買
产品编号
说明
价格
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
其他客户在看
International journal of molecular sciences, 20(24) (2020-01-01)
Metabolomics/lipidomics are important tools to identify novel biomarkers associated with liver damage. Patients with chronic liver disease (CLD) and hepatitis C virus (HCV) infection often have alterations in glucose, lipid and protein metabolism. The aim of this study was to
Biochimica et biophysica acta. Molecular and cell biology of lipids, 1865(4), 158609-158609 (2020-01-10)
STARD4, a member of the evolutionarily conserved START gene family, is a soluble sterol transport protein implicated in cholesterol sensing and maintenance of cellular homeostasis. STARD4 is widely expressed and has been shown to transfer sterol between liposomes as well
Biochemistry, 28(12), 5113-5120 (1989-06-13)
The critical micelle concentration (cmc) of several lysophospholipids and of a lysophospholipid analogue was determined from surface tension measurements using the maximum bubble pressure method and/or 31P NMR. The use of the maximum bubble pressure method has now been extended
Biochemistry, 57(39), 5759-5767 (2018-09-18)
Deleterious mutations in the serine hydrolase DDHD domain containing 1 (DDHD1) cause the SPG28 subtype of the neurological disease hereditary spastic paraplegia (HSP), which is characterized by axonal neuropathy and gait impairments. DDHD1 has been shown to display PLA1-type phospholipase
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