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FMOC-D-苯丙氨酸

FMOC-D-苯丙氨酸用途

Fmoc-D-Phe-OH是苯丙氨酸衍生物[1]。

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FMOC-D-苯丙氨酸名称

[ CAS 号 ]:
86123-10-6

[ 中文名 ]:
Fmoc-D-苯丙氨酸

[ 英文名 ]:
Fmoc-D-Phe-OH

[中文别名 ]:

[英文别名 ]:

Fmoc-(D)-Phe-NH2
(R)-Fmoc-phenylalanine
fmoc-d-phe
N-Fmoc-D-phenylalanine
Fmoc-D-Phe-OH
Fmoc-D-phenylalanine-OH
MFCD00062955
Fmoc-D-phenylalanine
Fmoc-phenylalanine

FMOC-D-苯丙氨酸生物活性

[ 描述 ]:

Fmoc-D-Phe-OH是苯丙氨酸衍生物[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):1793-815.

FMOC-D-苯丙氨酸物理化学性质

[ 密度 ]:
1.3±0.1 g/cm3

[ 沸点 ]:
620.1±50.0 °C at 760 mmHg

[ 熔点 ]:
181-185ºC

[ 分子式 ]:
C₂₄H₂₁NO₄

[ 分子量 ]:
387.428

[ 闪点 ]:
328.8±30.1 °C

[ 精确质量 ]:
387.147064

[ PSA ]:
75.63000

[ LogP ]:
5.41

[ 外观性状 ]:
白色粉末

[ 蒸汽压 ]:
0.0±1.9 mmHg at 25°C

[ 折射率 ]:
1.633

[ 储存条件 ]:
2-8°C

FMOC-D-苯丙氨酸MSDS

FMOC-D-苯丙氨酸安全信息

[ 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

[ 海关编码 ]:
2924299090

FMOC-D-苯丙氨酸合成路线

FMOC-D-苯丙氨酸上下游产品

FMOC-D-苯丙氨酸上游产品

FMOC-D-苯丙氨酸下游产品

FMOC-D-苯丙氨酸海关

[ 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%

FMOC-D-苯丙氨酸文献

1,4-disubstituted-[1,2,3]triazolyl-containing analogues of MT-II: design, synthesis, conformational analysis, and biological activity.

J. Med. Chem. 57(22) , 9424-34, (2014)

Side chain-to-side chain cyclizations represent a strategy to select a family of bioactive conformations by reducing the entropy and enhancing the stabilization of functional ligand-induced receptor c...

Solid-phase synthesis of C-terminal azapeptides.

J. Pept. Sci. 21 , 387-91, (2015)

The solid-phase synthesis of azapeptides possessing a C-terminal aza-residue has been accomplished by a protocol featuring regioselective alkylation of benzhydrylidene-aza-glycinamide and illustrated ...

Preclinical evaluation of a high-affinity 18F-trifluoroborate octreotate derivative for somatostatin receptor imaging.

J. Nucl. Med. 55(9) , 1499-505, (2014)

Recent studies have highlighted the high sensitivity of PET imaging with (68)Ga-labeled octreotide derivatives for the detection and staging of neuroendocrine tumors. A somatostatin receptor ligand th...

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