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47517

Sigma-Aldrich

Fmoc-Hyp(tBu)-OH

≥98.0% (HPLC)

Synonyme(s) :

Fmoc-O-tert-butyl-L-hydroxyproline

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About This Item

Formule empirique (notation de Hill):
C24H27NO5
Numéro CAS:
122996-47-8
Poids moléculaire :
409.47
Numéro Beilstein :
6161467
Numéro MDL:
MFCD00151930
Code UNSPSC :
12352209
eCl@ss :
32160406
ID de substance PubChem :
57650984
Nomenclature NACRES :
NA.26

Pureté

≥98.0% (HPLC)

Activité optique

[α]20/D −25±2.5°, c = 1% in methanol

Capacité de réaction

reaction type: Fmoc solid-phase peptide synthesis

Application(s)

peptide synthesis

Groupe fonctionnel

Fmoc

Température de stockage

2-8°C

Chaîne SMILES 

CC(C)(C)O[C@@H]1C[C@H](N(C1)C(=O)OCC2c3ccccc3-c4ccccc24)C(O)=O

InChI

1S/C24H27NO5/c1-24(2,3)30-15-12-21(22(26)27)25(13-15)23(28)29-14-20-18-10-6-4-8-16(18)17-9-5-7-11-19(17)20/h4-11,15,20-21H,12-14H2,1-3H3,(H,26,27)/t15-,21+/m1/s1

Clé InChI

WPBXBYOKQUEIDW-VFNWGFHPSA-N

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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Fmoc-tBu-Gly-OH ≥98.0%

Sigma-Aldrich

47524

Fmoc-tBu-Gly-OH

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International journal of molecular sciences, 19(11) (2018-11-08)
Herein, we describe a modified form of the antimicrobial hairpin-like peptide EcAMP1, isolated from barnyard grass (E. crusgalli) seeds, which is structurally characterized by a combination of high-pressure liquid chromatography, mass spectrometry, and automated Edman sequencing. This derivate has a
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Toxicon : official journal of the International Society on Toxinology, 130, 1-10 (2017-02-28)
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Lucas L Bennink et al.
Biomaterials, 183, 67-76 (2018-08-28)
Degradation of the extracellular matrix (ECM) is one of the fundamental factors contributing to a variety of life-threatening or disabling pathological conditions. However, a thorough understanding of the degradation mechanism and development of new ECM-targeting diagnostics are severely hindered by
Yang Li et al.
Macromolecular bioscience, 15(1), 52-62 (2014-12-06)
To address the downside of conventional photo-patterning which can alter the chemical composition of protein scaffolds, we developed a non-covalent photo-patterning strategy for gelatin (denatured collagen) hydrogels that utilizes UV activated triple helical hybridization of caged collagen mimetic peptide (caged

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