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生物来源
synthetic
检测方案
≥75% (TLC)
形式
crystalline
官能团
carboxylic acid
脂质类型
phosphoglycerides
储存温度
−20°C
SMILES字符串
[Na+].CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC
InChI
1S/C42H82NO10P.Na/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-40(44)50-35-38(36-51-54(48,49)52-37-39(43)42(46)47)53-41(45)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2;/h38-39H,3-37,43H2,1-2H3,(H,46,47)(H,48,49);/q;+1/p-1/t38-,39+;/m1./s1
InChI key
SJRBMGBLPUBGJL-MBAWARMDSA-M
应用
在胆固醇-磷脂混合物的相变研究中,胆固醇在凝胶相中与DSPS的混溶性要比液晶相中弱得多;最高50 mol%的胆固醇并不能消除烃链熔融相变。
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Journal of lipid research, 58(9), 1884-1892 (2017-07-27)
Compartmentalization of metabolism into specific regions of the cell, tissue, and organ is critical to life for all organisms. Mass spectrometric imaging techniques have been valuable in identifying and quantifying concentrations of metabolites in specific locations of cells and tissues
PloS one, 5(1), e8546-e8546 (2010-01-06)
We consider the problem of optimizing a liposomal drug formulation: a complex chemical system with many components (e.g., elements of a lipid library) that interact nonlinearly and synergistically in ways that cannot be predicted from first principles. The optimization criterion
PLoS pathogens, 9(3), e1003232-e1003232 (2013-04-05)
Human T-cell Immunoglobulin and Mucin-domain containing proteins (TIM1, 3, and 4) specifically bind phosphatidylserine (PS). TIM1 has been proposed to serve as a cellular receptor for hepatitis A virus and Ebola virus and as an entry factor for dengue virus.
Membranes, 10(11) (2020-11-19)
Pharmacological efficiency of active compounds is largely determined by their membrane permeability. Thus, identification of drug-membrane interactions seems to be a crucial element determining drug-like properties of chemical agents. Yet, knowledge of this issue is still lacking. Since chemoprevention based
Antimicrobial agents and chemotherapy, 63(4) (2019-02-06)
The present study aimed to clarify the mechanism underlying the high distribution of lascufloxacin in epithelial lining fluid (ELF). Involvement of transporters was examined by transcellular transport across Calu-3 and transporter-overexpressing cells; the binding of lascufloxacin to ELF components was
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