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Key Documents

Altri documenti

47378

Sigma-Aldrich

Fmoc-D-Phe-OH

≥98.0%

Sinonimo/i:

Fmoc-D-phenylalanine

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About This Item

Formula empirica (notazione di Hill):
C24H21NO4
Numero CAS:
86123-10-6
Peso molecolare:
387.43
Beilstein:
4767931
Numero MDL:
MFCD00062955
Codice UNSPSC:
12352209
eCl@ss:
32160406
ID PubChem:
57650934
NACRES:
NA.26

Saggio

≥98.0%

Impiego in reazioni chimiche

reaction type: Fmoc solid-phase peptide synthesis

applicazioni

peptide synthesis

Gruppo funzionale

Fmoc

Temperatura di conservazione

2-8°C

Stringa SMILE

OC(=O)[C@@H](Cc1ccccc1)NC(=O)OCC2c3ccccc3-c4ccccc24

InChI

1S/C24H21NO4/c26-23(27)22(14-16-8-2-1-3-9-16)25-24(28)29-15-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h1-13,21-22H,14-15H2,(H,25,28)(H,26,27)/t22-/m1/s1
SJVFAHZPLIXNDH-JOCHJYFZSA-N

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Descrizione
Determinazione del prezzo

914436

Fmoc-D-Lys(Biotin)-OH, ≥95%

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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Sigma-Aldrich

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D-Phenylalanine

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Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 55(9), 1499-1505 (2014-06-28)
Recent studies have highlighted the high sensitivity of PET imaging with (68)Ga-labeled octreotide derivatives for the detection and staging of neuroendocrine tumors. A somatostatin receptor ligand that is easily radiolabeled with (18)F-fluoride could improve the availability of PET imaging of
Charles A Galea et al.
Biochemistry, 56(4), 657-668 (2017-01-11)
Polymyxins remain one of the few antibiotics available for treating antibiotic resistant bacteria. Here we describe polymyxin B thioesterase which performs the final step in polymyxin B biosynthesis. Isolated thioesterase catalyzed cyclization of an N-acetylcystamine polymyxin B analogue to form
Oliver John V Belleza et al.
MedChemComm, 9(10), 1673-1678 (2018-11-16)
Nobilamide B, a TRPV1 antagonist, and a series of Ala-substituted analogues were synthesized and their neuroactivity was assessed in a primary culture of dorsal root ganglion (DRG) neurons. Analogues 4, 6, and 7 showed comparable activity, affecting capsaicin response in
Kazuma Ogawa et al.
Chemical & pharmaceutical bulletin, 66(6), 651-659 (2018-06-05)
Radiolabeled cyclic peptides containing the (Arg-Gly-Asp) RGD sequence for use in positron emission tomography (PET) imaging, single-photon emission computed tomography (SPECT) imaging, and targeted radionuclide therapy of cancer have been reported. In this study, RGD was used as a model
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
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