B2251
5-Benzyloxy-DL-tryptophan
crystalline
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关于此项目
经验公式（希尔记法）:
C18H18N2O3
化学文摘社编号:
分子量:
310.35
UNSPSC Code:
12352200
PubChem Substance ID:
EC Number:
228-980-7
MDL number:
InChI key
DFGNDJBYANKHIO-UHFFFAOYSA-N
InChI
1S/C18H18N2O3/c19-16(18(21)22)8-13-10-20-17-7-6-14(9-15(13)17)23-11-12-4-2-1-3-5-12/h1-7,9-10,16,20H,8,11,19H2,(H,21,22)
SMILES string
NC(Cc1c[nH]c2ccc(OCc3ccccc3)cc12)C(O)=O
assay
≥98% (TLC)
form
crystalline
color
light yellow
storage temp.
−20°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)
法规信息
新产品
此项目有
T M Crone et al.
Carcinogenesis, 16(8), 1687-1692 (1995-08-01)
Although the human O6-alkylguanine-DNA alkyltransferase (AGT) is very sensitive to inactivation by O6-benzylguanine (BG) or 2,4-diamino-6-benzyloxy-5-nitrosopyrimidine (5-nitroso-BP), the equivalent protein formed by the carboxyl terminal domain of the product of the Escherichia coli ada gene (Ada-C) is unaffected by these
L T Kushashvili et al.
Antibiotiki i khimioterapiia = Antibiotics and chemoterapy [sic], 33(1), 16-22 (1988-01-01)
The process of asymmetric deacylation of an acetyl derivative of 5-benzyl hydroxytryptophan racemate in the presence of native microbial aminoacylase was studied. The effect of pH, temperature, concentration of the enzyme and substrate were investigated. Conditions for preparation and isolation
K Iseki et al.
Biochimica et biophysica acta, 1146(1), 121-126 (1993-02-23)
The uptake mechanisms of organic cations such as tryptamine, tyramine, 5-benzyloxytryptamine (BOTA) and their zwitterionic derivatives (tyrosine, tryptophan, 5-benzyloxytryptophan (BOTP)) by rat intestinal brush-border membrane vesicles and liposome containing phosphatidylserine were studied and compared. As compared to their zwitterionic derivatives
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