Quantification of L- and D-enantiomers of proline, trans-4-hydroxyproline and cis-4-hydroxyproline in natural samples using differential labelling with 12C- and 13C6-dabsyl chloride, chiral separation and liquid chromatography-mass spectrometry.

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Title: Quantification of L- and D-enantiomers of proline, trans-4-hydroxyproline and cis-4-hydroxyproline in natural samples using differential labelling with 12C- and 13C6-dabsyl chloride, chiral separation and liquid chromatography-mass spectrometry.
Authors: Rai B; Department of Nutrition, Koshien University, 10-1 Momijigaoka, Takarazuka, Hyogo 665-0006, Japan., Ishida T; Department of Nutrition, Koshien University, 10-1 Momijigaoka, Takarazuka, Hyogo 665-0006, Japan.
Source: Journal of biochemistry [J Biochem] 2026 Jul 01; Vol. 180 (1), pp. 33-48.
Publication Type: Journal Article
Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0376600 Publication Model: Print Cited Medium: Internet ISSN: 1756-2651 (Electronic) Linking ISSN: 0021924X NLM ISO Abbreviation: J Biochem Subsets: MEDLINE
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  Data: Quantification of L- and D-enantiomers of proline, trans-4-hydroxyproline and cis-4-hydroxyproline in natural samples using differential labelling with 12C- and 13C6-dabsyl chloride, chiral separation and liquid chromatography-mass spectrometry.
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  Data: <searchLink fieldCode="AU" term="%22Rai+B%22">Rai B</searchLink>; Department of Nutrition, Koshien University, 10-1 Momijigaoka, Takarazuka, Hyogo 665-0006, Japan.<br /><searchLink fieldCode="AU" term="%22Ishida+T%22">Ishida T</searchLink>; Department of Nutrition, Koshien University, 10-1 Momijigaoka, Takarazuka, Hyogo 665-0006, Japan.
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  Data: <searchLink fieldCode="JN" term="%220376600%22">Journal of biochemistry</searchLink> [J Biochem] 2026 Jul 01; Vol. 180 (1), pp. 33-48.
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        Value: 10.1093/jb/mvag020
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      – Code: eng
        Text: English
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        StartPage: 33
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      – TitleFull: Quantification of L- and D-enantiomers of proline, trans-4-hydroxyproline and cis-4-hydroxyproline in natural samples using differential labelling with 12C- and 13C6-dabsyl chloride, chiral separation and liquid chromatography-mass spectrometry.
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            NameFull: Rai B
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            NameFull: Ishida T
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              Text: 2026 Jul 01
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              Y: 2026
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