1948-71-6
- Product Name:N-Acetyl-L-tyrosinamide
- Molecular Formula:C11H14N2O3
- Purity:99%
- Molecular Weight:
Product Details;
CasNo: 1948-71-6
Molecular Formula: C11H14N2O3
Appearance: white crystalline powder
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N-Acetyl-L-tyrosinamide 1948-71-6 In Bulk Supply
- Molecular Formula:C11H14N2O3
- Molecular Weight:222.244
- Appearance/Colour:white crystalline powder
- Vapor Pressure:3.49E-14mmHg at 25°C
- Melting Point:223-225 °C(lit.)
- Refractive Index:1.576
- Boiling Point:459.53 °C at 760 mmHg
- Flash Point:231.716 °C
- PSA:92.42000
- Density:1.253 g/cm3
- LogP:1.01590
1948-71-6 Usage
N-Acetyl-L-tyrosinamide is a monomer model compound for PLT, while it's Molecular Formula is C11H14N2O3. N-Acetyl-L-tyrosine Amide is an analogue of L-tyrosine which stimulate the transport of L-Tyr, mainly by the ASC system. N-acetyl-l-tyrosinamide is a model for Tyr present in proteins. In the N-acetyl-l-tyrosinamide system, only Tyr amino acids are present and only π...π aromatic interactions are possible.
InChI:InChI=1/C11H14N2O3/c1-7(14)13-10(11(12)16)6-8-2-4-9(15)5-3-8/h2-5,10,15H,6H2,1H3,(H2,12,16)(H,13,14)/t10-/m0/s1
1948-71-6 Relevant articles
Three-photon excitation of N-acetyl-L-tyrosinamide
I Gryczynski, H Malak, JR Lakowicz
, Biophysical chemistry, 1999
We observed emission from the tyrosine derivative N-acetyl-l-tyrosinamide (NATyrA) when excited with the fundamental output of a femtosecond Ti:Sapphire laser from 780 to 855 nm. …
Reaction of Diisopropylphosphorofluoridate with N-Acetyl-L-tyrosinamide
T Inagami, T MURACHI
, The Journal of Biochemistry, 1970
The alkylphosphorylation of the phenolic oxy gen of tyrosine by DFP** was first reported by Ashbolt and Rydon (1). Later on, similar reaction involving tyrosyl residues of proteins has …
1948-71-6 Process route
- 537-55-3
N-acetyl-L-tyrosine
- 1948-71-6
N-acetyl-L-tryrosinamide
Conditions | Yield |
---|---|
With dmap; ammonium chloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 0 - 20 ℃;
|
- 2440-79-1
N-acetyl-L-tyrosine methyl ester
- 1948-71-6
N-acetyl-L-tryrosinamide
Conditions | Yield |
---|---|
With ammonia; at -40 ℃;
|
|
With ammonia;
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1948-71-6 Upstream products
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N-acetyl-L-tyrosine ethyl ester
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2440-79-1
N-acetyl-L-tyrosine methyl ester
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DL-tryptophanamide radical
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1948-71-6 Downstream products
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503157-91-3
N-α-acetyl-O-(tert-butyl(dimethyl)silyl)-L-tyrosinamide
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503157-93-5
N-α-(acetyl-tert-butoxycarbonyl)-N,N-di(tert-butoxycarbonyl)-L-tyrosinamide
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