CAS 17355-23-6: N,O-Diacetyl-L-tyrosine
Formula:C13H15NO5
InChI:InChI=1S/C13H15NO5/c1-8(15)14-12(13(17)18)7-10-3-5-11(6-4-10)19-9(2)16/h3-6,12H,7H2,1-2H3,(H,14,15)(H,17,18)/t12-/m0/s1
InChI key:InChIKey=ZUAVWNTVXZCOEL-LBPRGKRZSA-N
SMILES:C([C@H](NC(C)=O)C(O)=O)C1=CC=C(OC(C)=O)C=C1
Synonyms:- (S)-2-Acetamido-3-(4-acetoxyphenyl)propanoic acid
- <span class="text-smallcaps">L</span>-Tyrosine, N,O-diacetyl-
- <span class="text-smallcaps">L</span>-Tyrosine, N-acetyl-, acetate (ester)
- Ac-Tyr(Ac)-OH
- N,O-Diacetyl-<span class="text-smallcaps">L</span>-tyrosine
- N,O-diacetyl-L-tyrosine
- N-acetyl-O-acetyl-L-tyrosine
- O,N-Diacetyl-<span class="text-smallcaps">L</span>-tyrosine
- Tyrosine, N-acetyl-, acetate (ester), <span class="text-smallcaps">L</span>-
- L-Tyrosine, N,O-diacetyl-
- O,N-Diacetyl-L-tyrosine
- See more synonyms
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Found 5 products.
N,O-Bis-acetyl-L-tyrosine
CAS:N,O-Bis-acetyl-L-tyrosine is a bioreversible acetylated amino acid that is synthesized from L-tyrosine. It can be used in the preparation of creatine kinase. N,O-Bis-acetyl-L-tyrosine has been shown to bind to the aromatic residues on creatine kinase and inhibit its activity. The acetylation of lysine residues may be reversible, but this process requires the presence of a hydroxyl group on the tyrosine residue. This reaction is catalyzed by a lysine residue on creatine kinase. Studies have shown that the kinetic properties of N,O-Bis-acetyl-L-tyrosine are similar to those of L-tyrosine and therefore it can be used as an alternative substrate for creatine biosynthesis.Formula:C13H15NO5Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:265.26 g/molL-Tyrosine, N,O-diacetyl-
CAS:Formula:C13H15NO5Purity:95%Color and Shape:SolidMolecular weight:265.2619(S)-2-Acetamido-3-(4-acetoxyphenyl)propanoic acid
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:265.2650146484375
