Identification | Back Directory | [Name]
Z-GLN-GLY-OH | [CAS]
6610-42-0 | [Synonyms]
Z-GLN-GLY NSC 186901 Z-GLN-GLY-OH na-cbz-gln-gly Z-GLN-GLY-OH,>98% -5-oxopentanamido) N-ALPHA-CBZ-GLN-GLY Z-L-GLUTAMINYL-GLYCINE Z-GLN-GLY-OH USP/EP/BP Z-L-GLUTAMINYL-L-GLYCINE -2-(5-Amino-2-(((benzyloxy) Nalpha-carbobenzyloxy-Gln-Gly Carbobenzoxy-L-glutaminylglycine Z-GLN-GLY, GAMMA-GLUTAMYL DONOR SUBS BENZYLOXYCARBONYL-L-GLUTAMINYLGLYCINE α-N-carbobenzyloxy-L-glutamine-glycine N-BENZYLOXYCARBONYL-L-GLUTAMINYLGLYCINE Z-Gln-Gly gamma-glutamyl donor substrate N2-[(Phenylmethoxy)carbonyl]-L-glutaminylglycine Glycine, N2-[(phenylmethoxy)carbonyl]-L-glutaminyl- 2-[(4-carbamoyl-2-phenylmethoxycarbonylamino-butanoyl)amino]acetic acid 2-[(2S)-2-{[(benzyloxy)carbonyl]amino}-4-carbamoylbutanamido]acetic acid 2-[[5-amino-5-oxo-2-(phenylmethoxycarbonylamino)pentanoyl]amino]aceticaci (S)-2-(5-aMino-2-(((benzyloxy)carbonyl)aMino)-5-oxopentanaMido)acetic acid 2-[[5-amino-5-oxo-2-(phenylmethoxycarbonylamino)pentanoyl]amino]acetic acid 2-[[(2S)-5-amino-5-oxo-2-(phenylmethoxycarbonylamino)pentanoyl]amino]acetic acid | [Molecular Formula]
C15H19N3O6 | [MDL Number]
MFCD00055926 | [MOL File]
6610-42-0.mol | [Molecular Weight]
337.33 |
Chemical Properties | Back Directory | [Melting point ]
131 - 132°C | [Boiling point ]
748.0±60.0 °C(Predicted) | [density ]
1.339 | [storage temp. ]
-20°C | [solubility ]
Chloroform (Slightly, Sonicated) Methanol (Slightly), Water (Slightly, Sonicated | [form ]
Solid | [pka]
3.38±0.10(Predicted) | [color ]
White to Off-White |
Hazard Information | Back Directory | [Uses]
γ-Glutamyl donor substrate used in spectrophotometric determination of transglutaminase (TGase) activity. Z-Gln-Gly was used to enzymatically synthesize N-linked neoglycoproteins. | [Biochem/physiol Actions]
N-Benzyloxycarbonyl-L-Glutaminylglycine (Z-Gln-Gly, Z-QG) is used as a substrate to differentiate and characterize transglutaminase(s) (TGase) that catalyzes the post-translational covalent cross-linking of Gln- and Lys-containing peptides. Z-QG supports glutamyl-level cross-linking applications thruough surface modification. |
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