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Merck
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文件

772054

Sigma-Aldrich

Fmoc-D-Lys(Boc)-OH

98%, for peptide synthesis

别名:

Nα-Fmoc-N-ε-Boc-D-lysine

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About This Item

经验公式（希尔记法）:
C26H32N2O6
CAS号:
92122-45-7
分子量:
468.54
MDL號碼:
MFCD00065660
分類程式碼代碼:
12352209
PubChem物質ID:
329767535
NACRES:
NA.26

product name

Fmoc-D-Lys(Boc)-OH, 98%

品質等級

100

化驗

98%

形狀

powder or crystals

反應適用性

reaction type: Fmoc solid-phase peptide synthesis

mp

128-131 °C

應用

peptide synthesis

官能基

Boc
Fmoc

儲存溫度

2-8°C

SMILES 字串

CC(C)(C)OC(=O)NCCCC[C@@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

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

InChI 密鑰

UMRUUWFGLGNQLI-JOCHJYFZSA-N

相关类别

相關產品

产品编号
说明
价格

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

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Nicholas J Kenyon et al.
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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
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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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