2-氨基-3-(甲硫基)丁酸

2-氨基-3-(甲硫基)丁酸用途

DL-4-硫芥酸是一种异亮氨酸衍生物[1]。

2-氨基-3-(甲硫基)丁酸名称

[ CAS 号 ]:
443-80-1

[ 中文名 ]:
2-氨基-3-(甲硫基)丁酸

[ 英文名 ]:
2-AMINO-3-[METHYLTHIO]BUTYRIC ACID

[中文别名 ]:

[英文别名 ]:

DL-4-Thiaisoleucine
DL-thiaisoleucine
4-Thiaisoleucine
2-Amino-3-methylmercapto-buttersaeure
MFCD00056745

2-氨基-3-(甲硫基)丁酸生物活性

[ 描述 ]:

DL-4-硫芥酸是一种异亮氨酸衍生物[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.

2-氨基-3-(甲硫基)丁酸物理化学性质

[ 密度 ]:
1.202g/cm3

[ 沸点 ]:
280.1ºC at 760 mmHg

[ 分子式 ]:
C₅H₁₁NO₂S

[ 分子量 ]:
149.21100

[ 闪点 ]:
123.2ºC

[ 精确质量 ]:
149.05100

[ PSA ]:
88.62000

[ LogP ]:
0.85010

[ 蒸汽压 ]:
0.00103mmHg at 25°C

[ 折射率 ]:
1.528

2-氨基-3-(甲硫基)丁酸安全信息

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

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

[ WGK德国 ]:
3

[ 海关编码 ]:
2930909090

2-氨基-3-(甲硫基)丁酸海关

[ 海关编码 ]: 2930909090

[ 中文概述 ]:
2930909090. 其他有机硫化合物. 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:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

2-氨基-3-(甲硫基)丁酸文献

Validation of isoleucine utilization targets in Plasmodium falciparum.

Proc. Natl. Acad. Sci. U. S. A. 108 , 1627-1632, (2011)

Intraerythrocytic malaria parasites can obtain nearly their entire amino acid requirement by degrading host cell hemoglobin. The sole exception is isoleucine, which is not present in adult human hemog...

Isopenicillin N synthase binds δ-(L-α-aminoadipoyl)-L-cysteinyl-D-thia-allo-isoleucine through both sulfur atoms.

ChemBioChem. 12 , 1881-1885, (2011)

Isopenicillin N synthase (IPNS) catalyses the synthesis of isopenicillin N (IPN), the biosynthetic precursor to penicillin and cephalosporin antibiotics. IPNS is a non-heme iron(II) oxidase that media...

Incorporation of amino acid analogs interferes with the processing of the asparagine-linked oligosaccharide of the MOPC-46B kappa light chain.

J. Biol. Chem. 257 , 9039-9042, (1982)

The incorporation of the leucine analog, beta-hydroxyleucine, or the isoleucine analog, 4-thiaisoleucine, into the MPOC-46B kappa chain interfered with the processing of the oligosaccharide moiety of ...

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