1945
DOI: 10.1016/s0021-9258(18)43108-0
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The Antiriboflavin Effect of Galactoflavin

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1946
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Cited by 25 publications
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“…(5) A quite different picture emerges on oxidation of L-cysteinyl.ocysteine or D-cysteinyl-L-cysteine at these two pH values. 4 The corre spending peptides of cystine, except for their optical enantiomorphism, appeared to be identical, and independent of the ¿H at which they were formed. They crystallized from water with no evidence of water of crystallization, yielded a single ninhydrin spot on the paper chromatogram with Rt * 0.16 (phenol) for each, and on HC1 hydrolysis gave good yields of DL-cystine.…”
Section: Resultsmentioning
confidence: 95%
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“…(5) A quite different picture emerges on oxidation of L-cysteinyl.ocysteine or D-cysteinyl-L-cysteine at these two pH values. 4 The corre spending peptides of cystine, except for their optical enantiomorphism, appeared to be identical, and independent of the ¿H at which they were formed. They crystallized from water with no evidence of water of crystallization, yielded a single ninhydrin spot on the paper chromatogram with Rt * 0.16 (phenol) for each, and on HC1 hydrolysis gave good yields of DL-cystine.…”
Section: Resultsmentioning
confidence: 95%
“…Preparation of Peptides.-The peptides of L-cystine were prepared substantially as described in part I of this series. 4 Both benzyl groups of S-benzyl-L-cysteinyl-L-cysteine were removed by reduction using sodium in liquid ammonia, and the resulting L-cysteinyl-L-cysteine purified as the insoluble mercury mercaptide. Decomposition of the mercury derivative was effected with hydrogen sulfide, and, after filtration from mercury sulfide, the solution was freed from excess hydrogen sulfide by evaporation in vacuo.…”
Section: Methodsmentioning
confidence: 99%
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