| Identification | Back Directory | [Name]
H-HIS-BETANA | [CAS]
7424-15-9 | [Synonyms]
H-His-bNA
L-His-βNA
H-His-βNA
H-His-βNA
H-HIS-BETANA
HISTIDINE-BETANA
L-histidine B-naphthylamide
L-Histidine β-naphthylamide
L-histidine 2-naphthylamide
l-histidine β-naphthylamide
L-HISTIDYL-BETA-NAPHTHYLAMIDE
L-HISTIDINE BETA-NAPHTHYLAMIDE
L-Histidine β-naphthylaMide powder
(S)-alpha-amino-N-2-naphthyl-1H-imidazole-4-propionamide
(S)-α-Amino-N-(2-naphthalenyl)-1H-imidazole-4-propanamide
1H-Imidazole-5-propanamide, α-amino-N-2-naphthalenyl-, (αS)- | [EINECS(EC#)]
231-052-4 | [Molecular Formula]
C16H16N4O | [MDL Number]
MFCD00051166 | [MOL File]
7424-15-9.mol | [Molecular Weight]
280.32 |
| Hazard Information | Back Directory | [Uses]
L-Histidine β-naphthylamide is a histidine derivative[1]. | [Definition]
ChEBI: An L-histidine derivative that is the amide obtained by formal condensation of the carboxy group of L-histidine with the amino group of 2-naphthylamine. | [Biological Activity]
L-Histidine β-naphthylamide is an analogue of L-histidine used to study structural roles of L-histidine in functions such as the activation of HutP protein transcription. L-Histidine β-naphthylamide may also be used to study the specificity and kinetics of various proteases and peptidases. | [References]
[1] Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. DOI:10.1080/10408398.2012.708368 |
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| Company Name: |
Energy Chemical
|
| Tel: |
021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
| Company Name: |
Merck KGaA
|
| Tel: |
21-20338288 |
| Website: |
www.sigmaaldrich.cn |
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