772054
Fmoc-D-Lys(Boc)-OH
98%, for peptide synthesis
别名:
Nα-Fmoc-N-ε-Boc-D-lysine
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关于此项目
经验公式（希尔记法）:
C26H32N2O6
化学文摘社编号:
分子量:
468.54
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26
MDL number:
产品名称
Fmoc-D-Lys(Boc)-OH, 98%
SMILES string
CC(C)(C)OC(=O)NCCCC[C@@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
InChI key
UMRUUWFGLGNQLI-JOCHJYFZSA-N
InChI
1S/C26H32N2O6/c1-26(2,3)34-24(31)27-15-9-8-14-22(23(29)30)28-25(32)33-16-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h4-7,10-13,21-22H,8-9,14-16H2,1-3H3,(H,27,31)(H,28,32)(H,29,30)/t22-/m1/s1
assay
98%
form
powder or crystals
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
mp
128-131 °C
application(s)
peptide synthesis
functional group
Boc
Fmoc
storage temp.
2-8°C
Quality Level
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Nicholas J Kenyon et al.
PloS one, 8(10), e77730-e77730 (2013-11-10)
Nanocarriers can deliver a wide variety of drugs, target them to sites of interest, and protect them from degradation and inactivation by the body. They have the capacity to improve drug action and decrease undesirable systemic effects. We have previously
Jingfang Li et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(54), 13510-13517 (2017-07-12)
A series of cationic peptides with alternating hydrophilic and hydrophobic residues were elaborately designed and synthesized. These kinds of short peptides with protonated lysine groups can interact with anionic polyoxometalate nanoclusters through multivalent ionic bonds and hydrogen bonds, resulting in
Si Chen et al.
Biomaterials, 117, 92-104 (2016-12-13)
In this work, mitochondria-targeting gold nanostar (AuNS) and anticarcinogen DOX were co-encapsulated in hyaluronic acid (HA) protective shell for tumor-targeting synergistic photothermal/chemo-therapy. Cationic peptide R
Andreas Pech et al.
Nucleic acids research, 45(7), 3997-4005 (2017-02-06)
Biological evolution resulted in a homochiral world in which nucleic acids consist exclusively of d-nucleotides and proteins made by ribosomal translation of l-amino acids. From the perspective of synthetic biology, however, particularly anabolic enzymes that could build the mirror-image counterparts
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