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关于此项目
经验公式(希尔记法):
C26H50O11
化学文摘社编号:
分子量:
538.67
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5458950
InChI
1S/C26H50O11/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-34-25-23(33)21(31)24(18(16-28)36-25)37-26-22(32)20(30)19(29)17(15-27)35-26/h17-33H,2-16H2,1H3/t17-,18-,19-,20+,21-,22-,23-,24-,25-,26-/m1/s1
SMILES string
CCCCCCCCCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O
InChI key
UKPROSIGWJBJGA-IWODYCRQSA-N
description
non-ionic
assay
≥99.0% (TLC)
form
solid
mol wt
538.67 g/mol
solubility
H2O: 10 mg/mL, clear, colorless
Quality Level
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
涉药品监管产品
此项目有
J Stöckel et al.
European journal of biochemistry, 248(3), 684-691 (1997-10-28)
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Dennis J Pillion et al.
Journal of pharmaceutical sciences, 91(6), 1456-1462 (2002-07-13)
A series of new glycosides with extended alkyl side-chains (C(13-16)) linked to maltose or sucrose were synthesized and tested for their efficacy in enhancing nasal insulin absorption in anesthetized rats. The new reagents were compared to previously tested alkylglycosides with
Modulation of acetylcholinesterase activity by glycoside-detergents and their solubilization efficiency for neuronal membranes from bovine nucleus caudatus.
P Landauer et al.
Biochemical and biophysical research communications, 106(3), 848-855 (1982-06-15)
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