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
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
EC Number:
228-333-9
Beilstein/REAXYS Number:
2212726
MDL number:
InChI key
GEYBMYRBIABFTA-VIFPVBQESA-N
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
SMILES string
COc1ccc(C[C@H](N)C(O)=O)cc1
assay
98%
optical activity
[α]25/D −7°, c = 0.5 in 1 M HCl
reaction suitability
reaction type: solution phase peptide synthesis
mp
259-261 °C (dec.) (lit.)
application(s)
peptide synthesis
storage temp.
2-8°C
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Debbie Dewaele et al.
Rapid communications in mass spectrometry : RCM, 30(6), 719-730 (2016-02-13)
Melphalan is a frequently used chemotherapeutical agent for the treatment of myeloma, breast cancer, ovarian cancer and sarcoma of soft tissue. A good knowledge of the reactivity of the drug toward the different amino acids, e.g. covalent adduct formation, is
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.
C Lee et al.
Biochemistry and molecular biology international, 31(5), 797-805 (1993-12-01)
An enzyme fraction with catalytic activities for the biosynthesis of the pipecolic acid containing cyclopeptolide SDZ 90-215 was partially purified and characterized from the genus Septoria. The crude cell homogenate was subjected to polyethyleneimine precipitation, ammonium sulfate precipitation and FPLC
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
Ning Wu et al.
Journal of the American Chemical Society, 126(44), 14306-14307 (2004-11-04)
We have developed a second orthogonal tRNA/synthetase pair for use in yeast based on the Escherichia coli tRNALeu/leucyl tRNA-synthetase pair. Using a novel genetic selection, we have identified a series of synthetase mutants that selectively charge the amber suppresor tRNA
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