
CAS 2566-19-0: N-cbz-gly-gly
Formula:C12H14N2O5
InChI:InChI=1/C12H14N2O5/c15-10(13-7-11(16)17)6-14-12(18)19-8-9-4-2-1-3-5-9/h1-5H,6-8H2,(H,13,15)(H,14,18)(H,16,17)
SMILES:c1ccc(cc1)COC(=NCC(=NCC(=O)O)O)O
Synonyms:- Z-Gly-Gly-OH
- N-CBZ-Glycylglycine N-Carbobenzyloxy-glycylglycine
- N-[(benzyloxy)carbonyl]glycylglycine
- Cbz-Gly-Gly
- Cbz-Glycine-Glycine
- Cbz-Gly-Gly-OH
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Found 7 products.
Z-Gly-Gly-OH
CAS:Bachem ID: 4000488.Formula:C12H14N2O5Purity:97.3%Color and Shape:WhiteMolecular weight:266.25Glycine, N-[N-[(phenylmethoxy)carbonyl]glycyl]-
CAS:Formula:C12H14N2O5Purity:95%Color and Shape:SolidMolecular weight:266.25(Carbobenzoxy)glycylglycine
CAS:Formula:C12H14N2O5Purity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:266.252-(2-(((Benzyloxy)carbonyl)amino)acetamido)acetic acid
CAS:Purity:95.0%Color and Shape:Solid, White to off-white powderMolecular weight:266.25299072265625N-[(Benzyloxy)carbonyl]glycylglycine
CAS:Applications N-[(Benzyloxy)carbonyl]glycylglycine is a reagent in the synthesis of Glycylglycyl-L-tyrosine (G718500), which is a fungal tyrosinases and their capability to oxidize peptide-bound tyrosine residues is important in a view of applicability of tyrosinases. References Bowness, J., et al.: Biochem. J., 53, 620 (1953), Cuff, M., et al.: J. Mol. Biol., 278, 855 (1998), Kubo, I., et al.: Bioorg. Med. Chem., 12, 5349 (2004),Formula:C12H14N2O5Color and Shape:NeatMolecular weight:266.25Z-Gly-Gly-OH
CAS:Z-Gly-Gly-OH is a soybean trypsin inhibitor that has been synthesized from wheat germ, and is used as an enzyme inhibitor. It has hydrolytic activity against soybean trypsin. The reaction time for the hydrolysis of Z-Gly-Gly-OH is about 10 minutes in an organic solvent at pH 7.5 and 25°C, with a ph optimum of about 8.5 to 9.5. The product is more stable than the substrate at high temperatures and low pH values, but less stable at high pH values, so it can be used as an enzyme inhibitor in a variety of conditions. Z-Gly- Gly-OH can also be immobilized on Sephadex G100 or sephadex G50 using ionic or covalent binding methods, which increases its stability and decreases the amount of byproducts produced during hydrolysis of the substrate.Formula:C12H14N2O5Purity:Min. 95%Molecular weight:266.25 g/mol