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Merck
CN

158259

O-甲基-L-酪氨酸

98%

别名:

4-甲氧基-L-苯丙氨酸

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关于此项目

线性分子式:
CH3OC6H4CH2CH(NH2)CO2H
化学文摘社编号:
分子量:
195.22
Beilstein:
2212726
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.22
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方案

98%

旋光性

[α]25/D −7°, c = 0.5 in 1 M HCl

反应适用性

reaction type: solution phase peptide synthesis

mp

259-261 °C (dec.) (lit.)

应用

peptide synthesis

储存温度

2-8°C

SMILES字符串

COc1ccc(C[C@H](N)C(O)=O)cc1

InChI

1S/C10H13NO3/c1-14-8-4-2-7(3-5-8)6-9(11)10(12)13/h2-5,9H,6,11H2,1H3,(H,12,13)/t9-/m0/s1

InChI key

GEYBMYRBIABFTA-VIFPVBQESA-N

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储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Rapid communications in mass spectrometry : RCM, 30(6), 719-730 (2016-02-13)
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Ma Diarey Tianero et al.
Nature microbiology, 4(7), 1149-1159 (2019-04-03)
Marine sponges often house small-molecule-producing symbionts extracellularly in their mesohyl, providing the host with a means of chemical defence against predation and microbial infection. Here, we report an intriguing case of chemically mediated symbiosis between the renieramycin-containing sponge Haliclona sp.
Jed N Lampe et al.
Journal of the American Chemical Society, 130(48), 16168-16169 (2008-11-13)
Conformational dynamics are thought to play an important role in ligand binding and catalysis by cytochrome P450 enzymes, but few techniques exist to examine them in molecular detail. Using a unique isotopic labeling strategy, we have site specifically inserted a
M Manning et al.
Journal of peptide science : an official publication of the European Peptide Society, 7(9), 449-465 (2001-10-06)
We report the solid phase synthesis of four pairs of L- and D-thienylalanine (Thi/D-Thi) position two modified analogues of the following four oxytocin (OT) antagonists: des-9-glycinamide [1-(beta-mercapto-beta,beta-pentamethylene propionic acid), 2-O-methyltyrosine, 4-threonine]ornithine-vasotocin (desGly(NH2)9,d (CH2)5[Tyr(Me)2,Thr4]OVT) (A); the Tyr-(NH2)9 analogue of (A), d(CH2)5[Tyr(Me)2,Thr4,Tyr-(NH2)9]OVT
Jeffrey K Takimoto et al.
ACS chemical biology, 6(7), 733-743 (2011-05-07)
Unnatural amino acids (Uaas) can be translationally incorporated into proteins in vivo using evolved tRNA/aminoacyl-tRNA synthetase (RS) pairs, affording chemistries inaccessible when restricted to the 20 natural amino acids. To date, most evolved RSs aminoacylate Uaas chemically similar to the

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