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检测方案
≥99.0% (HPLC)
形式
solid
mp
156-160 °C (dec.)
应用
peptide synthesis
SMILES字符串
Cn1cc(NC(=O)OC(C)(C)C)cc1C(O)=O
InChI
1S/C11H16N2O4/c1-11(2,3)17-10(16)12-7-5-8(9(14)15)13(4)6-7/h5-6H,1-4H3,(H,12,16)(H,14,15)
InChI key
GOLAEMFBWAIGRX-UHFFFAOYSA-N
其他说明
用于制备在生物技术中调节基因表达所需杂环芳族低聚酰胺的非天然氨基酸
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
E.E. Baird et al.
Journal of the American Chemical Society, 118, 6141-6141 (1996)
S White et al.
Nature, 391(6666), 468-471 (1998-02-14)
The design of synthetic ligands that read the information stored in the DNA double helix has been a long-standing goal at the interface of chemistry and biology. Cell-permeable small molecules that target predetermined DNA sequences offer a potential approach for
Karine Nozeret et al.
Biochimie, 149, 122-134 (2018-04-08)
Pericentromeric heterochromatin plays important roles in controlling gene expression and cellular differentiation. Fluorescent pyrrole-imidazole polyamides targeting murine pericentromeric DNA (major satellites) can be used for the visualization of pericentromeric heterochromatin foci in live mouse cells. New derivatives targeting human repeated
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