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Merck
CN

470058

Sigma-Aldrich

D-酪氨醇 盐酸盐

98%

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线性分子式:
4-(HO)C6H4CH2CH(NH2)CH2OH · HCl
CAS号:
分子量:
203.67
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

98%

旋光性

[α]22/D +18°, c = 1 in H2O

反应适用性

reaction type: solution phase peptide synthesis

mp

161-165 °C (lit.)

应用

peptide synthesis

SMILES字符串

Cl[H].N[C@@H](CO)Cc1ccc(O)cc1

InChI

1S/C9H13NO2.ClH/c10-8(6-11)5-7-1-3-9(12)4-2-7;/h1-4,8,11-12H,5-6,10H2;1H/t8-;/m1./s1

InChI key

PNGCRFWYSRUQTB-DDWIOCJRSA-N

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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M Angeles Gilabert et al.
Biological chemistry, 385(12), 1177-1184 (2005-01-18)
We report here on the stereospecificity observed in the action of horseradish peroxidase (HRPC) on monophenol and diphenol substrates. Several enantiomers of monophenols and o-diphenols were assayed: L-tyrosinol, D-tyrosinol, L-tyrosine, DL-tyrosine, D-tyrosine, L-dopa, DL-dopa, D-dopa, L-alpha-methyldopa, DL-alpha-methyldopa, DL-adrenaline, D-adrenaline, L-isoproterenol
C Monteilhet et al.
Journal of molecular biology, 173(4), 477-485 (1984-03-15)
Crystalline complexes of tyrosyl-tRNA synthetase from Bacillus stearothermophilus were prepared with adenosine, AMP, ATP and PPi, all in the presence of tyrosinol, which binds strongly to the tyrosine binding site but cannot be adenylated by ATP. The hydrolysis of ATP
Eric T Larson et al.
Journal of molecular biology, 409(2), 159-176 (2011-03-23)
The single tyrosyl-tRNA synthetase (TyrRS) gene in trypanosomatid genomes codes for a protein that is twice the length of TyrRS from virtually all other organisms. Each half of the double-length TyrRS contains a catalytic domain and an anticodon-binding domain; however
E M Newman et al.
Cancer research, 43(10), 4703-4708 (1983-10-01)
The effects of amino acid deprivation and treatment with amino alcohols upon the growth, viability, and susceptibility to methotrexate (MTX) cytotoxicity were examined in BALB/3T3 cells and their virally transformed counterparts, SV-T2 cells. Cells were deprived of either histidine or

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