Examples of 'cystamine' in a sentence
Meaning of "cystamine"
Cystamine is a chemical compound used in biochemical research and pharmaceuticals. In English, it is used in the context of science, medicine, or chemistry
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- The disulfide 2,2'-dithiobis(ethylamine)
How to use "cystamine" in a sentence
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cystamine
Enterically coated cysteamine bitartrate and cystamine.
Cystamine itself is a liquid at ambient temperatures.
A preferred reagent is cystamine dihydrochloride.
Cystamine and cystamine derivatives include sulfated cysteamnine.
An example of a linking group is cystamine.
Cystamine and genistein were both not effective in wt littermates.
Peptide synthesis is performed on the free amine of the cystamine.
Cystamine is an organic disulfide.
An excess amount of PAAc was used to ensure the complete reaction of cystamine.
Our research showed cystamine to facilitate biological and therapeutical effects of GSSG.
A suitable example of the linkers is cysteamine or its oxidised form cystamine.
The FGF analogue may be prepared with a cystamine protecting the thiol group of the cysteine.
The tablets are manufactured by first enterically coating the cysteamine or cystamine.
Cystamine and cysteamine were from Sigma.
An example of a suitable homobifunctional reagent for use in the invention includes cystamine.
See also
Enterically coated cysteamine, cystamine and derivatives thereof.
The electrode was then rinsed thoroughly with water to remove the unabsorbed cystamine.
That is, the cystamine molecules are strongly linked to the electrode surface.
Different pH conditions were used to test the conjugation efficiency between PAAc and cystamine.
In addition, cystamine was found to increase the levels of certain neuroprotective proteins.
The disclosure provides composition comprising enterically formulated cysteamine and cystamine derivatives.
Cystamine has similar side-effects and dosing difficulties to that of cysteamine.
The electrode was then rinsed thoroughly with water to remove the physically adsorbed cystamine.
Further, since cystamine is a primary amine, its use does not produce stable nitrosamines.
The stability was quantified by the fluorescamine assay which detected the amount of unreacted cystamine.
Coupling with Cystamine.
The following results were obtained with a representative compound of formula I in comparison with cystamine.
Cystamine shows faster rates and high states of cure, with minimum reversion.
A process according to claim 7 wherein the disulfide compound is cystamine.
The synthesis of the cystamine derivatives can be carried out according to two different methods,.
A composition according to claim 1, wherein the amine is cystamine or a salt thereof.
Reacting the activated saccharide with cystamine or cysteamine or a salt thereof, to produce a thiolated saccharide ;.
Scheme 5 shows a chemical reaction scheme for preparing a polyamidoamine containing cystamine residues ;.
Specific examples thereof include cysteine, cysteamine, cystamine and methionine, with cysteine being preferably used herein.
In a further preferred embodiment said disulfide containing compound is oxidized glutathione, cystine or cystamine.
Exemplary of suitable dendrimers are the starbust dendrimers, such as a cystamine core poly ( amidoamine ) PAMAM dendrimer.
Cystamine hydrochloride was added to a final concentration of 10 mM cystamine.
Once thiolated, a dialysis was performed to extract the excess of DTT and of cystamine.
The TG2 inhibitor cystamine is particularly preferred.
For example, such the derivative is GSSG • Pt covalently bound to phenylalanine or to cystamine.
The solution is made 40 mM cystamine dihydrochloride and stirred for one hour.
The activated saccharide is reacted with 1 mol . eq . of cystamine dihydrochloride.
Cystamine dihydrochloride is freshly prepared in anhydrous DMSO at a concentration of 50 mg / mL.
Second method, reaction between BOC-glycine activated by an ester and cystamine.
Unlabelled crystalline phenol ( 2 mg ) reacted smoothly with cystamine in HBr solution in a small scale reaction.
The unreacted cystamine is removed by size exclusion chromatography on a G-50 Sephadex column.
IGFBP-3 was refolded overnight following the addition of cystamine to a final concentration of 6 mM.
The disclosure provides enteric-coated cysteamine compositions ( sulfhydryl / Cystagon ™ ) and cystamine compositions.
However, it was possible to remove cystamine and accomplish preliminary purification using a Sep-pak C18 cartridge.
Figure 95, Dissolved oxygen and redox potential after cystamine addition.
