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甘氨酸苄酯盐酸盐

甘氨酸苄酯盐酸盐用途

H-DL-Gly-OBzl公司。HCl是甘氨酸(HY-Y0966)衍生物[1]。

甘氨酸苄酯盐酸盐名称

[ CAS 号 ]:
2462-31-9

[ 中文名 ]:
甘氨酸苄酯盐酸盐

[ 英文名 ]:
H-Gly-OBZl.HCl

[中文别名 ]:

[英文别名 ]:

GLYCINE-OBZL HCL
GLYCINE BENZYL ESTER HCL
Benzyl glycinate HCl
Benzyl glycinate hydrochloride (1:1)
Benzyl glycinate hyd
N-Bn-glycine hydrochloride
GLYCINE BENZYL ESTERHCI
MFCD00035442
GLY-OBZLCL
Glycine, phenylmethyl ester, hydrochloride (1:1)

甘氨酸苄酯盐酸盐生物活性

[ 描述 ]:

H-DL-Gly-OBzl公司。HCl是甘氨酸(HY-Y0966)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.

甘氨酸苄酯盐酸盐物理化学性质

[ 密度 ]:
1.132g/cm3

[ 沸点 ]:
245.5ºC at 760 mmHg

[ 熔点 ]:
138-140°C

[ 分子式 ]:
C₉H₁₂ClNO₂

[ 分子量 ]:
201.650

[ 闪点 ]:
110.3ºC

[ 精确质量 ]:
201.055649

[ PSA ]:
52.32000

[ LogP ]:
2.19080

[ 外观性状 ]:
白色至灰白色粉末

[ 蒸汽压 ]:
0.0146mmHg at 25°C

[ 折射率 ]:
1.558

[ 储存条件 ]:
−20°C

甘氨酸苄酯盐酸盐MSDS

甘氨酸苄酯盐酸盐安全信息

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

[ 危害码 (欧洲) ]:
Xi

[ 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

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甘氨酸苄酯盐酸盐文献

The Benzyl Ester Group of Amino Acid Monomers Enhances Substrate Affinity and Broadens the Substrate Specificity of the Enzyme Catalyst in Chemoenzymatic Copolymerization.

Biomacromolecules 17 , 314-23, (2016)

The chemoenzymatic polymerization of amino acid monomers by proteases involves a two-step reaction: the formation of a covalent acyl-intermediate complex between the protease and the carboxyl ester gr...

Synthesis of a metabolite of metoclopramide and its detection in human urine.

Il Farmaco 49 , 805-808, (1994)

The synthesis of 2-(4-amino-5-chloro-2-methoxybenzamido)acetic acid 2, a metabolite of metoclopramide 1, has been accomplished through the coupling of 4-amino-5-chloro-2-methoxybenzoic acid 4 with gly...

[Lengthening of the peptide chain at the C-terminal end of a glycosylamino acid].

Carbohydr. Res. 50 , 15-22, (1976)

An O-glycodipeptide was synthesized by lengthening the peptide chain on the C-terminal side of a glycosylamino acid unit. N-(Benzyloxycarbonyl)-3-O-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)-L-thr...

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