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47628

Sigma-Aldrich

Fmoc-Ile-OH

≥98.0% (T)

Sinônimo(s):

N-(9-Fluorenylmethoxycarbonyl)-L-isoleucine, Fmoc-L-isoleucine

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About This Item

Fórmula empírica (Notação de Hill):
C21H23NO4
Número CAS:
71989-23-6
Peso molecular:
353.41
Beilstein:
4716717
Número CE:
276-255-9
Número MDL:
MFCD00037125
Código UNSPSC:
12352209
eCl@ss:
32160406
ID de substância PubChem:
57651048
NACRES:
NA.26

Nível de qualidade

100

Ensaio

≥98.0% (T)

forma

solid

atividade óptica

[α]20/D −12±1°, c = 1% in DMF

adequação da reação

reaction type: C-H Activation
reaction type: Fmoc solid-phase peptide synthesis
reagent type: ligand
reaction type: Peptide Synthesis

pf

145-147 °C (lit.)

aplicação(ões)

peptide synthesis

grupo funcional

Fmoc
amine
carboxylic acid

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

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

InChI

1S/C21H23NO4/c1-3-13(2)19(20(23)24)22-21(25)26-12-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,13,18-19H,3,12H2,1-2H3,(H,22,25)(H,23,24)/t13-,19-/m0/s1

chave InChI

QXVFEIPAZSXRGM-DJJJIMSYSA-N

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Categorias relacionadas

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number
BCCD7459
BCCD7457
BCCD5472
BCBZ6720
BCBT4068

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We have previously described the photoactivated depot (PAD) approach for the light-stimulated release of therapeutic proteins such as insulin. The aim of this method is to release insulin from a shallow dermal depot in response to blood glucose information, using
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To apply motor proteins as natural nanomolecular machines to transporting systems in nanotechnology, complete temporal control over ON/OFF switching of the motility is necessary. We have studied the photoresponsive inhibition properties of azobenzene-tethered peptides for regulation of kinesin-microtubule motility. Although
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