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Acetyl-histidine

Protection was determined as described in Table 11. S026-B is from T4 lysozyme, P is from BPTl, (iNCT-pl and Fos-pl are leucine zippers Ac, acetyl. Histidines were ignored in determining net charge. Adapted from Randall (1992). C opyright 1992 by the AAAS. [Pg.179]

Neurosine N-acetyl-histidine Central nervous system and eyes 1964... [Pg.203]

As standards for spectrophotometric measurements, Traylor and Singer (1967) prepared the monoazo derivatives of histidine and tyrosine with the various diazonium salts. The spectra of the products of reaction of N-acetyl histidine with the diazonium salt were obtained after reaction of a 100-fold excess of N-acetyl histidine with the diazonium salt in 0.1 M borate at pH 9.0. The spectral constants for the histidine and tyrosine derivatives are recorded in Table 5.1. [Pg.161]

Park JS, Han TH, Lee KY, Han SS, Hwang JJ, Moon DH, Kim SY, Cho YW. N-acetyl histidine-conjugated glycol chitosan self-assembled nanoparticles for intracytoplasmic delivery of drugs Endocytosis, exocytosis and drug release. J Control Release 2006 115 37-45. [Pg.241]

Figure 3. 360 MHz H FT nmr spectra (10 pulsesl of 2.5 x 10"2 M N-acetyl histidine and 2 x lO" m flavin I at pH = 7.5 taken with the pulse sequence of Figure 1, (a) light spectrum, (bl dark spectrum, (c) difference a-b. The lower trace is a part of spectrum c with the vertical scale reduced by a factor 8. Figure 3. 360 MHz H FT nmr spectra (10 pulsesl of 2.5 x 10"2 M N-acetyl histidine and 2 x lO" m flavin I at pH = 7.5 taken with the pulse sequence of Figure 1, (a) light spectrum, (bl dark spectrum, (c) difference a-b. The lower trace is a part of spectrum c with the vertical scale reduced by a factor 8.
In N-acetyl-hlstidine such an Interaction between the positively charged a amino group and the lone pair at the N ir position Is not possible. The deprotonatlon of the Imidazole ring of that compound should result In shifts of Its N ir and N T resonances which are similar to those observed for histidine after deprotonatlon of the a amino group. Indeed we obtained values of the chemical shifts (-2oo.8 ppm and -169.o ppm) for the N ir zuid N t resonances of N-acetyl-histidine... [Pg.235]

Hence we have to consider a stacking association of a positively charged and a neutral imidazole ring of histidine. Ue obtain very similar results in the case of N-acetyl-histidine also which provides further evidence for this type of interaction. [Pg.246]

N-acetyl histidine-conjugated glycol chitosan self-assembled NPs For intracytoplasmic delivery of drugs [162]... [Pg.75]

The general procedure used in these studies is to trace-label samples of the protein with H-FDNB at several pH-values in the presence of N-acetyl-histidine or imidazole lactic acid as internal standard. The reaction mixture is then made chemically homogeneous by fully reacting with unlabelled or " C-FDNB. In the case of proteins containing more than one histidine residue, peptides are isolated so than an unequivocal assignment of parameters can be made. For proteins containing a solitary histidine residue, imidazolyl-DNP-histidine is isolated after acid hydrolysis. The internal standard is purified separately and the data from scintillation counting is substituted into Equations (1) or (2) to derive rate constants. [Pg.411]

Examples of micellar systems are given below where the surfactant provides the medium for catalysis but does not directly participate in the reaction. For instance, JV-acetyl histidine can bring about the hydrolysis of p-nitro-phenyl esters via an acyl-imidazole intermediate. [Pg.275]

N-Dodecyl-JV, N -dimethyl aminoethyl carbonate ion is hydrolyzed 2240 times faster with the following surfactant than with N-acetyl histidine. [Pg.278]

Bombesin peptide Bombesin was conjugated to JV-acetyl histidine-modified GC for targeting gastric-releasing peptide receptors overexpressed in prostate cancer cells. Iron oxide was loaded to be tested as a probe for MRI [34]... [Pg.145]


See other pages where Acetyl-histidine is mentioned: [Pg.181]    [Pg.541]    [Pg.547]    [Pg.556]    [Pg.755]    [Pg.225]    [Pg.585]    [Pg.215]    [Pg.215]    [Pg.236]    [Pg.242]    [Pg.219]    [Pg.245]    [Pg.175]    [Pg.61]    [Pg.145]    [Pg.282]   
See also in sourсe #XX -- [ Pg.240 ]




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N-Acetyl-L-histidine

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