![]() n-octyl-beta-d-maltopyranoside structure
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Common Name | n-octyl-beta-d-maltopyranoside | ||
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CAS Number | 82494-08-4 | Molecular Weight | 454.50900 | |
Density | 1.37g/cm3 | Boiling Point | 676.4ºC at 760 mmHg | |
Molecular Formula | C20H38O11 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 362.9ºC |
A large conformational change of the translocation ATPase SecA.
Proc. Natl. Acad. Sci. U. S. A. 101(30) , 10937-10942, (2004) The ATPase SecA mediates the posttranslational translocation of a wide range of polypeptide substrates through the SecY channel in the cytoplasmic membrane of bacteria. We have determined the crystal structure of a monomeric form of Bacillus subtilis SecA at ... |
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Comparison of alkylglycoside surfactants in enantioseparation by capillary electrophoresis.
Electrophoresis 18(6) , 912-918, (1997) Three alkylglycoside surfactants, namely n-octyl-beta-D-glucopyranoside (OG), n-nonyl-beta-D-glucopyranoside (NG), and n-octyl-beta-D-maltopyranoside (OM), were compared in the enantiomeric separation of dansyl amino acids, binaphthyl phosphate, bupivacaine a... |
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Binding of alkyl polyglucoside surfactants to bacteriorhodopsin and its relation to protein stability.
Biophys. J. 94(9) , 3647-3658, (2008) The binding of alkyl polyglucoside surfactants to the integral membrane protein bacteriorhodopsin (BR) and the formation of protein-surfactant complexes are investigated by sedimentation equilibrium via analytical ultracentrifugation and by small-angle neutro... |
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Capillary electrophoresis of herbicides: IV. Evaluation of octylmaltopyranoside chiral surfactant in the enantiomeric separation of fluorescently labeled phenoxy acid herbicides and their laser-induced fluorescence detection.
Electrophoresis 18(2) , 220-6, (1997) A novel chiral nonionic surfactant, namely octyl-b-D-maltopyranoside (OM), was evaluated in chiral capillary electrophoresis of fluorescently labeled phenoxy acid herbicides. The labeling of the analytes with 7-aminonaphthalene-1,3-disulfonic acid (ANDSA) per... |
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Nanocomposite formation between alpha-glucosyl stevia and surfactant improves the dissolution profile of poorly water-soluble drug.
Int. J. Pharm. 428(1-2) , 183-6, (2012) The formation of a hybrid-nanocomposite using α-glucosyl stevia (Stevia-G) and surfactant was explored to improve the dissolution of flurbiprofen (FP). As reported previously, the dissolution amount of FP was enhanced in the presence of Stevia-G, induced by t... |
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Capillary electrophoresis of herbicides. III. Evaluation of octylmaltopyranoside chiral surfactant in the enantiomeric separation of phenoxy acid herbicides.
Chirality 8(7) , 518-524, (1996) A chiral alkylglucoside surfactant, namely n-octyl-beta-D-maltopyranoside (OM), was evaluated in the enantiomeric separation of phenoxy acid herbicides. The enantiomeric resolution of the phenoxy acid herbicides could be manipulated readily by adjusting the s... |
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Alkylglycosides as artificial primers for glycogen biosynthesis.
Cell Mol. Biol. 43(3) , 369-81, (1997) Glycogenin is a 37 kDa self-glycosylating protein which has been demonstrated to be the initiating enzyme and primer for glycogen biosynthesis in liver, skeletal muscle and other tissues. We have recently shown that glycogenin will use alkylglucosides and alk... |