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- 英文名：
tert-Butyl 1-(3-Amino-5-fluoropyridin-4-yl)piperidine-4-carboxylate
- 库存：
100+
- 供应商：
上海维亦特生物
- CAS号：
1613192-01-0
tert-Butyl 1-(3-Amino-5-fluoropyridin-4-yl)piperidine-4-carboxylate
1613192-01-0
C₁₅H₂₂N₃O₂F
295.35
No Data Available
No Data Available
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文献和实验tert-Butyl 1-(3-Amino-5-fluoropyridin-4-yl)piperidine-4-carboxylate
1613192-01-0
C₁₅H₂₂N₃O₂F
295.35
No Data Available
No Data Available
Solid-Phase Synthesis of Neuropeptides by Fmoc Strategies
is used to protect the α-amino group of each residue. Those residues that have potentially reactive side chains are protected with acid-labile groups such as t-butyl. After removal of the Fmoc group with piperidine, the next protected amino
Synthesis and Probing of Membrane-bound Peptide Arrays
from their carboxyl termini using Fmoc-amino acid derivatives. After completion of the synthesis and cleavage of all side-chain protecting groups, the peptide array on the membrane is incubated with the potential interaction partners to identify their target sequences
Establishment of Stable Transfectant of CHO Lec Cells
mannose type, but differ in the number of mannoses, ranging from Man9 to Man5 . O-glycosylation is homogenous, with only a single GalNAc residue attached per site. When cultured in the presence of the alpha-glucosidase I inhibitor N-butyl
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