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L3877

D-Leu-Tyr

Name: <SC>D</SC>-Leu-Tyr
Brand: SIGMA

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About This Item

Formule empirique (notation de Hill):

C₁₅H₂₂N₂O₄

Numéro CAS:

3303-29-5

Poids moléculaire :

294.35

Numéro MDL:

MFCD00063034

Code UNSPSC :

12352200

ID de substance PubChem :

24896357

Température de stockage

−20°C

Chaîne SMILES

CC(C)C[C@@H](N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O

InChI

1S/C15H22N2O4/c1-9(2)7-12(16)14(19)17-13(15(20)21)8-10-3-5-11(18)6-4-10/h3-6,9,12-13,18H,7-8,16H2,1-2H3,(H,17,19)(H,20,21)/t12-,13+/m1/s1

Clé InChI

LHSGPCFBGJHPCY-OLZOCXBDSA-N

Actions biochimiques/physiologiques

D-Leucyltyrosine (D-Leu-Tyr) may be used to support the study of the uptake of oligopeptides by various peptide transport mechanisms.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number

072H0149

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Selective effect of zinc on uphill transport of oligopeptides into kidney brush border membrane vesicles.

H Daniel et al.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 9(11), 1112-1117 (1995-08-01)

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 concentrations

Reactivity of Tyr-Leu and Leu-Tyr dipeptides: identification of oxidation products by liquid chromatography-tandem mass spectrometry.

Conceição Fonseca et al.

Journal of mass spectrometry : JMS, 44(5), 681-693 (2009-01-07)

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-tyrosine (LY), by the hydroxyl

Molecular structures of L-Leu-L-Tyr, Gly-D,L-Met.p-toluenesulfonate and L-His-L-Leu.

J A Krause et al.

Acta crystallographica. Section B, Structural science, 49 ( Pt 1), 123-130 (1993-02-01)

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 =

Glycerol and glycerol carbonate as ultraviscous solvents for mixture analysis by NMR.

Pedro Lameiras et al.

Journal of magnetic resonance (San Diego, Calif. : 1997), 212(1), 161-168 (2011-08-02)

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

Identification of isomeric spin adducts of Leu-Tyr and Tyr-Leu free radicals using liquid chromatography-tandem mass spectrometry.

Pedro Domingues et al.

Biomedical chromatography : BMC, 26(1), 51-60 (2011-03-25)

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 during the oxidation of isomeric

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