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3-(1-萘基)丙氨酸

3-(1-萘基)丙氨酸用途

2-氨基-3-(萘-1-基)丙酸是丙氨酸衍生物[1]。

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3-(1-萘基)丙氨酸名称

[ CAS 号 ]:
28095-56-9

[ 中文名 ]:
DL-3-(1-萘基)-L-丙氨酸

[ 英文名 ]:
1-Naphthalenealanine

[中文别名 ]:

3-(1-萘基)丙氨酸

[英文别名 ]:

L66J B1YZVQ
2-amino-3-naphthalen-1-ylpropanoic acid
1-naphthalanine
3-(1-Naphthyl)-DL-alanine
3-(1-Naphthyl)alanine
D,L-β-(1-Naphthyl)alanine
1-Naphthalenealanine
D,L-1-naphthylalanine
2-Amino-3-(1-naphthyl)propanoic acid
1-Naphthalenepropanoic acid, α-amino-

3-(1-萘基)丙氨酸生物活性

[ 描述 ]:

2-氨基-3-(萘-1-基)丙酸是丙氨酸衍生物[1]。

[ 相关类别 ]:

研究领域 >> 其他

信号通路 >> 其他 >> 其他

[体外研究]

氨基酸和氨基酸衍生物已被商业化用作能量补充剂。它们影响合成代谢激素的分泌、运动期间的燃料供应、压力相关任务期间的精神表现,并防止运动引起的肌肉损伤。它们被认为是有益的能生膳食物质[1]。

[参考文献]

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1077.

3-(1-萘基)丙氨酸物理化学性质

[ 密度 ]:
1.3±0.1 g/cm3

[ 沸点 ]:
412.3±33.0 °C at 760 mmHg

[ 熔点 ]:
239℃

[ 分子式 ]:
C₁₃H₁₃NO₂

[ 分子量 ]:
215.248

[ 闪点 ]:
203.2±25.4 °C

[ 精确质量 ]:
215.094635

[ PSA ]:
63.32000

[ LogP ]:
2.34

[ 蒸汽压 ]:
0.0±1.0 mmHg at 25°C

[ 折射率 ]:
1.660

[ 储存条件 ]:
2-8°C

3-(1-萘基)丙氨酸MSDS

3-(1-萘基)丙氨酸安全信息

[ 个人防护装备 ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ 海关编码 ]:
2922499990

3-(1-萘基)丙氨酸合成路线

3-(1-萘基)丙氨酸上下游产品

3-(1-萘基)丙氨酸上游产品

3-(1-萘基)丙氨酸下游产品

3-(1-萘基)丙氨酸海关

[ 海关编码 ]: 2922499990

[ 中文概述 ]:
2922499990 其他氨基酸及其酯及它们的盐（含有一种以上含氧基的除外）. 增值税率:17.0% 退税率:9.0% 监管条件:AB(入境货物通关单,出境货物通关单) 最惠国关税:6.5% 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乙醇胺及其盐应报明色度, 乙醇胺及其盐应报明包装

[ 监管条件 ]: A.入境货物通关单 B.出境货物通关单

[ 检验检疫 ]: P.进境动植物、动植物产品检疫 Q.出境动植物、动植物产品检疫 R.进口食品卫生监督检验 S.出口食品卫生监督检验 M.进口商品检验 N.出口商品检验

[ Summary ]:
HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0%

3-(1-萘基)丙氨酸文献

Synthesis and characterization of more potent analogues of hirudin fragment 1-47 containing non-natural amino acids.

Biochemistry 37(39) , 13507-15, (1998)

Hirudin is the most potent and specific inhibitor of thrombin, a key enzyme in the coagulation process existing in equilibrium between its procoagulant (fast) and anticoagulant (slow) form. In a previ...

The A14 position of insulin tolerates considerable structural alterations with modest effects on the biological behavior of the hormone.

J. Protein Chem. 11(5) , 571-7, (1992)

As part of our aim to investigate the contribution of the tyrosine residue found in the 14 position of the A-chain to the biological activity of insulin, we have synthesized six insulin analogues in w...

Adding L-3-(2-Naphthyl)alanine to the genetic code of E. coli.

J. Am. Chem. Soc. 124 , 1836-1837, (2002)

An unnatural amino acid, L-3-(2-naphthyl)alanine, has been site-specifically incorporated into proteins in Escherichia coli. An orthogonal aminoacyl-tRNA synthetase was evolved that uniquely aminoacyl...

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