The use of 3-bromopropionic acid for the determination of protein thiol groups
Keyword(s):
S-Carboxymethylcysteine, formed by the reaction of iodoacetic acid with cysteine, was found to undergo intramolecular cyclization to yield 3-oxo-(2H,3H,5H,6H-1,4-thiazine)-5-carboxylic acid. The cyclization was studied under various conditions and the product was isolated and characterized. S-Carboxyethylcysteine, formed by the reaction of 3-bromopropionic acid with cysteine, did not undergo the cyclization reaction. The use of 3-bromopropionic acid was examined as an alternative to iodoacetic acid for the protection and determination of protein thiol groups.
1969 ◽
Vol 32
(1)
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pp. 106-117
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1997 ◽
Vol 151
(1)
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pp. 47-55
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2008 ◽
Vol 864
(1-2)
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pp. 38-42
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2010 ◽
Vol 30
(7)
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pp. 675-684
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