![]() H-D-Leu-Tyr-OH structure
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Common Name | H-D-Leu-Tyr-OH | ||
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CAS Number | 3303-29-5 | Molecular Weight | 294.34600 | |
Density | 1.218 g/cm3 | Boiling Point | 560ºC at 760 mmHg | |
Molecular Formula | C15H22N2O4 | Melting Point | 260 °C | |
MSDS | USA | Flash Point | 292.5ºC |
Glycerol and glycerol carbonate as ultraviscous solvents for mixture analysis by NMR.
J. Magn. Reson. 212(1) , 161-8, (2011) NMR of weakly polar analytes in an apolar ultraviscous solvent has recently been proposed for mixture analysis as a pertinent alternative to the DOSY experiment. The present article reports the first use of glycerol and glycerol carbonate as polar solvents fo... |
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Identification of isomeric spin adducts of Leu-Tyr and Tyr-Leu free radicals using liquid chromatography-tandem mass spectrometry.
Biomed. Chromatogr. 26(1) , 51-60, (2012) Free radical species are generally short-lived due to their high reactivity and thus direct measurement and identification are often impossible. In this study we used a spin trap, 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), to trap radical intermediates formed d... |
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Molecular structures of L-Leu-L-Tyr, Gly-D,L-Met.p-toluenesulfonate and L-His-L-Leu.
Acta Crystallogr. B 49 ( Pt 1) , 123-30, (1993) L-Leu-L-Tyr, (I), C15H22N2O4, M(r) = 294.35, crystallizes from MeOH/5% dimethyl sulfoxide in the orthorhombic space group P2(1)2(1)2(1). a = 5.644 (1), b = 12.094 (3), c = 22.548 (4) A, V = 1539.0 (5) A3, Z = 4, Dx = 1.270 g cm-3, Cu K alpha, lambda = 1.54184... |
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Selective effect of zinc on uphill transport of oligopeptides into kidney brush border membrane vesicles.
FASEB J. 9 , 1112-1117, (1995) Based on the involvement of zinc in hydrolysis of peptides, we hypothesized that Zn2+ may also play a role in peptide transport. To investigate this hypothesis, kidney brush border membrane vesicles (BBMV) were incubated for 30 min with different concentratio... |
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Reactivity of Tyr-Leu and Leu-Tyr dipeptides: identification of oxidation products by liquid chromatography-tandem mass spectrometry.
J. Mass Spectrom. 44(5) , 681-93, (2009) The exposure of peptides and proteins to reactive hydroxyl radicals results in covalent modifications of amino acid side-chains and protein backbone. In this study we have investigated the oxidation the isomeric peptides tyrosine-leucine (YL) and leucine-tyro... |
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