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Cbz-L-苯丙氨醇

Cbz-L-苯丙氨醇用途

Z-苯丙氨酸是丙氨酸衍生物[1]。

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Cbz-L-苯丙氨醇名称

[ CAS 号 ]:
6372-14-1

[ 中文名 ]:
Z-L-苯丙氨醇

[ 英文名 ]:
(S)-Cbz-Phenylalaninol

[中文别名 ]:

[英文别名 ]:

Benzyl (1-hydroxy-3-phenylpropan-2-yl)carbamate
MFCD00191138
Z-Phenylalaninol
Z-Phe-ol

Cbz-L-苯丙氨醇生物活性

[ 描述 ]:

Z-苯丙氨酸是丙氨酸衍生物[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):1793-1110.

Cbz-L-苯丙氨醇物理化学性质

[ 密度 ]:
1.2±0.1 g/cm3

[ 沸点 ]:
489.0±45.0 °C at 760 mmHg

[ 熔点 ]:
90-94ºC

[ 分子式 ]:
C₁₇H₁₉NO₃

[ 分子量 ]:
285.338

[ 闪点 ]:
249.6±28.7 °C

[ 精确质量 ]:
285.136505

[ PSA ]:
58.56000

[ LogP ]:
3.25

[ 外观性状 ]:
固体;White to Almost white powder to crystal

[ 蒸汽压 ]:
0.0±1.3 mmHg at 25°C

[ 折射率 ]:
1.583

[ 储存条件 ]:
2~8°C

Cbz-L-苯丙氨醇MSDS

详细MSDS(安全技术说明书)

Cbz-L-苯丙氨醇安全信息

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

[ 危害码 (欧洲) ]:
T+

[ 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 ]:
2924299090

Cbz-L-苯丙氨醇上下游产品

Cbz-L-苯丙氨醇上游产品

Cbz-L-苯丙氨醇下游产品

Cbz-L-苯丙氨醇海关

[ 海关编码 ]: 2924299090

[ 中文概述 ]:
2924299090. 其他环酰胺（包括环氨基甲酸酯）（包括其衍生物以及他们的盐）. 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:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 包装

[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Cbz-L-苯丙氨醇文献

Preparation of Aminoalkyl Chlorohydrin Hydrochlorides: Key Building Blocks for Hydroxyethylamine-Based HIV Protease Inhibitors.

J. Org. Chem. 61 , 3635, (1996)

Enantiomerically pure N,N-dibenzyl-alpha-amino aldehydes reacted with (chloromethyl)lithium, generated in situ from bromochloromethane and lithium metal, to give predominantly erythro aminoalkyl epoxi...

Stereoselective Synthesis of HIV-1 Protease Inhibitor, DMP 323.

J. Org. Chem. 61 , 444, (1996)

DMP 323, a potent HIV-1 protease inhibitor, has been synthesized by an efficient stereoselective process, amenable to large scale preparations. The core C(2) symmetric diol was synthesized by a stereo...

Cyclic HIV protease inhibitors: synthesis, conformational analysis, P2/P2' structure-activity relationship, and molecular recognition of cyclic ureas.

J. Med. Chem. 39 , 3514, (1996)

High-resolution X-ray structures of the complexes of HIV-1 protease (HIV-1PR) with peptidomimetic inhibitors reveal the presence of a structural water molecule which is hydrogen bonded to both the mob...

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