A6751
N-Acetyl-L-tyrosine ethyl ester monohydrate
≥98%, suitable for ligand binding assays
Synonym(s):
ATEE
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About This Item
Empirical Formula (Hill Notation):
C13H17NO4 · H2O
CAS Number:
Molecular Weight:
269.29
Beilstein:
2217900
EC Number:
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26
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Product Name
N-Acetyl-L-tyrosine ethyl ester monohydrate,
Assay
≥98%
Quality Level
form
powder
technique(s)
ligand binding assay: suitable
color
white
storage temp.
−20°C
SMILES string
CCOC(=O)[C@H](Cc1ccc(O)cc1)NC(C)=O
InChI
1S/C13H17NO4/c1-3-18-13(17)12(14-9(2)15)8-10-4-6-11(16)7-5-10/h4-7,12,16H,3,8H2,1-2H3,(H,14,15)/t12-/m0/s1
InChI key
SKAWDTAMLOJQNK-LBPRGKRZSA-N
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Application
N-Acetyl-L-tyrosine ethyl ester monohydrate has been used:
- as a substrate in transesterification reactions with 1 M propan-1-ol catalyzed by Carlsberg protease protein-coated microcrystals (PCMC)
- to test the performance of subtilisin Carlsberg protein-coated microcrystals (PCMC)
- as a substrate for cross-linked crystals (CLECs) of subtilisin activity screening
Biochem/physiol Actions
N-Acetyl-L-tyrosine ethyl ester is an N-terminal and C-terminal protected L-tyrosine that is used in crosslinking studies and as a substrate for the detection, differentiation and/or characterization various proteases and esterases.
Substrates
Substrate for chymotrypsin
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Acta crystallographica. Section C, Crystal structure communications, 63(Pt 10), o572-o575 (2007-10-06)
The crystal structure of a protected L-tyrosine, namely N-acetyl-L-tyrosine methyl ester monohydrate, C(12)H(15)NO(4).H(2)O, was determined at both 293 (2) and 123 (2) K. The structure exhibits a network of O-H...O and N-H...O hydrogen bonds, in which the water molecule plays
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To evaluate if unconjugated bilirubin (UB) inhibits C1 esterase activity. Esterase activity was evaluated by C1-mediated hydrolysis of N-acetyl-L-tyrosine ethyl ester, and binding of UB to C1r and C1s was assessed by dot-blot analysis. UB inhibited C1 enzymatic activity. C1r
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A study of the intermolecular interactions of tolmetin/N-acetyl-L-tyrosine ethyl ester complex.
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Spectrochimica Acta Part A: Molecular Spectroscopy, 72, 1000-1006 (2009)
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