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关于此项目
经验公式(希尔记法):
C16H20N2O4
化学文摘社编号:
分子量:
304.34
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
236-072-7
MDL number:
Beilstein/REAXYS Number:
39677
Quality Level
assay
≥99.0% (TLC)
optical activity
[α]20/D −20±1°, c = 1% in DMF
reaction suitability
reaction type: Boc solid-phase peptide synthesis
mp
136 °C (dec.) (lit.)
application(s)
peptide synthesis
SMILES string
CC(C)(C)OC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(O)=O
InChI
1S/C16H20N2O4/c1-16(2,3)22-15(21)18-13(14(19)20)8-10-9-17-12-7-5-4-6-11(10)12/h4-7,9,13,17H,8H2,1-3H3,(H,18,21)(H,19,20)/t13-/m0/s1
InChI key
NFVNYBJCJGKVQK-ZDUSSCGKSA-N
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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)
Peroxidase catalyzed nitration of tryptophan derivatives
Sala A, et al.
European Journal of Biochemistry, 271(13), 2841-2852 (2004)
Bailey T , et al. et al.
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 21 (2014)
Y Kato et al.
Biochemical and biophysical research communications, 234(1), 82-84 (1997-05-08)
The aim of this study was to clarify the mechanism of loss of Trp residues in proteins exposed to peroxynitrite. The Trp residues in bovine serum albumin and collagen IV were decreased by peroxynitrite treatment. To identify the degradation products
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 15512-1L-R | 04061838741912 |
| 15512-2.5L-R | 04061838125125 |
| 15512-5G-F | 04061832641621 |
| 15512-25KG-R | 04061838125132 |
| 15512-4X2.5L-R | 04061838741929 |
| 15512-5L-R | 04061838118127 |
| 15512-6X1L-R | 04061838118134 |