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47317

Sigma-Aldrich

Fmoc-Lys(Fmoc)-OH

≥98.0% (HPLC)

Sinónimos:

Nα,Nε-di-Fmoc-L-lysine

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About This Item

Fórmula empírica (notación de Hill):
C36H34N2O6
Número de CAS:
78081-87-5
Peso molecular:
590.66
Beilstein/REAXYS Number:
6034060
MDL number:
MFCD00080275
UNSPSC Code:
12352209
PubChem Substance ID:
57650922
NACRES:
NA.26

Quality Level

100

assay

≥98.0% (HPLC)

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

OC(=O)[C@H](CCCCNC(=O)OCC1c2ccccc2-c3ccccc13)NC(=O)OCC4c5ccccc5-c6ccccc46

InChI

1S/C36H34N2O6/c39-34(40)33(38-36(42)44-22-32-29-17-7-3-13-25(29)26-14-4-8-18-30(26)32)19-9-10-20-37-35(41)43-21-31-27-15-5-1-11-23(27)24-12-2-6-16-28(24)31/h1-8,11-18,31-33H,9-10,19-22H2,(H,37,41)(H,38,42)(H,39,40)/t33-/m0/s1

InChI key

BMJRTKDVFXYEFS-XIFFEERXSA-N

Categorías relacionadas

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
BCCJ5359
BCBW9055
BCBF8531V
BCBT4641
BCBR8529V

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Joseph R Merrill et al.
Biomaterials, 84, 241-249 (2016-02-04)
Tumor angiogenesis, the formation of new tumor blood supply, has been recognized as a hallmark of cancer and represents an important target for clinical management of various angiogenesis-dependent solid tumors. Previously, by screening a bacteriophage peptide library we have discovered
Alex Abramov et al.
Molecules (Basel, Switzerland), 24(1) (2018-12-24)
In this work we have investigated the potential benefits of using supramolecular gel networks as reaction media to carry out air-sensitive metal-free light-induced trifluoromethylation of six-membered (hetero)arenes under aerobic conditions. This reaction was performed at room temperature (RT) using sodium
Shafq Al-Azzawi et al.
International journal of molecular sciences, 19(10) (2018-10-21)
Alzheimer's disease (AD) is a progressive brain disorder and age-related disease characterised by abnormal accumulation of β-amyloid (Aβ). The development of drugs to combat AD is hampered by the lack of therapeutically-active molecules able to cross the blood-brain barrier (BBB).
Andrew G Cheetham et al.
Acta pharmacologica Sinica, 38(6), 874-884 (2017-03-07)
The conjugation of small molecular hydrophobic anticancer drugs onto a short peptide with overall hydrophilicity to create self-assembling drug amphiphiles offers a new prodrug strategy, producing well-defined, discrete nanostructures with a high and quantitative drug loading. Here we show the
Jumpei Omi et al.
Nature communications, 11(1), 162-162 (2020-01-11)
The emergence of drug-resistant influenza type A viruses (IAVs) necessitates the development of novel anti-IAV agents. Here, we target the IAV hemagglutinin (HA) protein using multivalent peptide library screens and identify PVF-tet, a peptide-based HA inhibitor. PVF-tet inhibits IAV cytopathicity
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