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L-脯氨酰胺

L-脯氨酰胺用途

L-脯氨酸酰胺是脯氨酸衍生物[1]。

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L-脯氨酰胺名称

[ CAS 号 ]:
7531-52-4

[ 中文名 ]:
L-脯氨酰胺

[ 英文名 ]:
L-Prolinamide

[中文别名 ]:

[英文别名 ]:

(S)-Prolinamide
2-Pyrrolidinecarboxamide, (S)-
(2S)-2-Pyrrolidinecarboxamide
h-pro-nh2
2-Pyrrolidinecarboximidic acid, (2S)-
(S)-Pyrrolidine-2-carboxylic acid amide
MFCD00005253
(2S)-2-Pyrrolidinecarboximidic acid
EINECS 231-397-0
2-Pyrrolidinecarboxamide, (2S)-

L-脯氨酰胺生物活性

[ 描述 ]:

L-脯氨酸酰胺是脯氨酸衍生物[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):1793-1144.

L-脯氨酰胺物理化学性质

[ 密度 ]:
1.1±0.1 g/cm3

[ 沸点 ]:
303.6±31.0 °C at 760 mmHg

[ 熔点 ]:
95-97 °C(lit.)

[ 分子式 ]:
C₅H₁₀N₂O

[ 分子量 ]:
114.146

[ 闪点 ]:
137.4±24.8 °C

[ 精确质量 ]:
114.079315

[ PSA ]:
55.12000

[ LogP ]:
-1.51

[ 外观性状 ]:
白色结晶粉末

[ 蒸汽压 ]:
0.0±0.6 mmHg at 25°C

[ 折射率 ]:
1.491

[ 储存条件 ]:
室温，干燥，密封

[ 水溶解性 ]:
可溶于：甲醇

L-脯氨酰胺MSDS

L-脯氨酰胺安全信息

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

[ 危害码 (欧洲) ]:
Xn: Harmful;

[ 风险声明 (欧洲) ]:
R22

[ 安全声明 (欧洲) ]:
S22-S24/25

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

[ WGK德国 ]:
3

[ 海关编码 ]:
2933990090

L-脯氨酰胺合成路线

L-脯氨酰胺上下游产品

L-脯氨酰胺上游产品

L-脯氨酰胺下游产品

L-脯氨酰胺海关

[ 海关编码 ]: 2933990090

[ 中文概述 ]:
2933990090. 其他仅含氮杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乌洛托品请注明外观, 6－己内酰胺请注明外观, 签约日期

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

L-脯氨酰胺文献

Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...

Enantioseparation of amino acids and alpha-hydroxy acids on ligand-exchange continuous beds by capillary electrochromatography.

Electrophoresis 31 , 1517-1520, (2010)

A new chiral stationary phase based on continuous bed (CB) technology using L-prolinamide as a chiral selector was prepared. Its ability for enantioseparation of amino acids and alpha-hydroxy acids by...

d-Glucosamine in a chimeric prolinamide organocatalyst for direct asymmetric aldol addition

Carbohydr. Res. 356 , 273-7, (2012)

O-TBDPS D-glucosamine coupled with l-proline is reported to act as an efficient organocatalyst in the accomplishment of direct aldol reactions. Excellent results, in terms of chemical yields, as well ...

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