50110
甘氨酸甲酯 盐酸盐
puriss., ≥99.0% (AT)
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关于此项目
线性分子式:
NH2CH2COOCH3 · HCl
化学文摘社编号:
分子量:
125.55
EC Number:
227-139-1
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
3593644
MDL number:
InChI key
COQRGFWWJBEXRC-UHFFFAOYSA-N
InChI
1S/C3H7NO2.ClH/c1-6-3(5)2-4;/h2,4H2,1H3;1H
SMILES string
Cl.COC(=O)CN
grade
puriss.
assay
≥99.0% (AT)
ign. residue
≤0.05%
mp
175 °C (dec.) (lit.), 175-176 °C (dec.)
法规信息
新产品
此项目有
L K Frankel et al.
Biochemistry, 38(43), 14271-14278 (1999-11-26)
The effects of the modification of carboxylate groups on the manganese-stabilizing protein of photosystem II were investigated. Carboxylate groups (including possibly the C-terminus) on the manganese-stabilizing protein were modified with glycine methyl ester in a reaction facilitated by 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide. The
K W Kuo et al.
International journal of peptide and protein research, 46(2), 181-185 (1995-08-01)
To study the functional involvements of the common interaction of the Leu-1 alpha-amino group and Asp-58 in cobrotoxin, the lysine epsilon-amino groups of cobrotoxin were initially guanidinated with o-methylisourea. The alpha-amino group of Leu-1 was them modified with TNBS after
D Levy
Biochimica et biophysica acta, 317(2), 473-481 (1973-08-30)
A procedure has been described for the modification of the amino group of glycine methyl ester, and the amino groups of the hormone, insulin, with the reagent p-nitrophenyl-p-chloromercuribenzoate, effecting the introduction of the chloromercuri group at various defined sites in
Glycine enolates: the large effect of iminium ion formation on alpha-amino carbon acidity.
A Rios et al.
Journal of the American Chemical Society, 123(32), 7949-7950 (2001-08-09)
D Solís et al.
Analytical biochemistry, 209(1), 117-122 (1993-02-15)
The usefulness of ricin as a research tool is handicapped by its extremely biohazardous nature. In this work, ricin toxicity has been reduced by chemical modification of carboxyl groups using 1-ethyl-3(3-dimethylaminopropyl) carbodiimide and [14C]glycine methyl ester. The reaction was carried
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