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(S)-2-氨基-3-(5-氟-1H-吲哚-3-基)丙酸

(S)-2-氨基-3-(5-氟-1H-吲哚-3-基)丙酸名称

[ CAS 号 ]:
16626-02-1

[ 中文名 ]:
L-5-氟色氨酸

[ 英文名 ]:
DL-5-Fluorotryptophan

[中文别名 ]:

[英文别名 ]:

2-amino-3-(5-fluoro-1H-indol-3-yl)propanoic acid
5-Fluoro-DL-tryptophan
5-Fluoro D,L-tryptophan
5-Fluoro-D,L-tryptophan
5-Fluorotryptophan
UNII:5IC9663SHW
Tryptophan, 5-fluoro-

(S)-2-氨基-3-(5-氟-1H-吲哚-3-基)丙酸物理化学性质

[ 密度 ]:
1.4±0.1 g/cm3

[ 沸点 ]:
450.7±45.0 °C at 760 mmHg

[ 分子式 ]:
C₁₁H₁₁FN₂O₂

[ 分子量 ]:
222.216

[ 闪点 ]:
226.4±28.7 °C

[ 精确质量 ]:
222.080460

[ PSA ]:
79.11000

[ LogP ]:
1.17

[ 蒸汽压 ]:
0.0±1.2 mmHg at 25°C

[ 折射率 ]:
1.673

[ 储存条件 ]:
2-8°C，避光，保存于惰性气体中

(S)-2-氨基-3-(5-氟-1H-吲哚-3-基)丙酸MSDS

(S)-2-氨基-3-(5-氟-1H-吲哚-3-基)丙酸安全信息

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

[ 安全声明 (欧洲) ]:
22-24/25

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

[ 海关编码 ]:
2933990090

(S)-2-氨基-3-(5-氟-1H-吲哚-3-基)丙酸合成路线

(S)-2-氨基-3-(5-氟-1H-吲哚-3-基)丙酸上下游产品

(S)-2-氨基-3-(5-氟-1H-吲哚-3-基)丙酸上游产品

(S)-2-氨基-3-(5-氟-1H-吲哚-3-基)丙酸下游产品

(S)-2-氨基-3-(5-氟-1H-吲哚-3-基)丙酸海关

[ 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%

(S)-2-氨基-3-(5-氟-1H-吲哚-3-基)丙酸文献

Glucose recognition proteins for glucose sensing at physiological concentrations and temperatures.

ACS Chem. Biol. 9(7) , 1595-602, (2014)

Advancements in biotechnology have allowed for the preparation of designer proteins with a wide spectrum of unprecedented chemical and physical properties. A variety of chemical and genetic methods ca...

Substrate promiscuity of the cyclic dipeptide prenyltransferases from Aspergillus fumigatus ( section sign).

J. Nat. Prod. 72 , 44-52, (2009)

This study reports that a series of tryptophan derivatives with modifications on the side chain or at the indole ring were accepted by two cyclic dipeptide prenyltransferases, CdpNPT and FtmPT1, and c...

Hydrophobic effect and hydrogen bonds account for the improved activity of a complement inhibitor, compstatin.

J. Med. Chem. 49(15) , 4616-22, (2006)

Tryptophans at positions 4 and 7 of compstatin, a peptide complement inhibitor, are crucial for its interaction with C3. However, the nature of their involvement has not been studied to date. Here we ...

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