914339

Fmoc-L-Lys(Nvoc)-OH

≥98%

• Sinónimos: (S)-2-(((9H-Fluoren-9-yl)methoxy)carbonylamino)-6-((4,5-dimethoxy-2-nitrobenzyloxy)carbonylamino)hexanoic acid, N₂-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N₆-(((4,5-dimethoxy-2-nitrobenzyl)oxy)carbonyl)-L-lysine, Lysine with photoremovable NVOC, Photocaged amino acid, Photocleavable lysine derivative
• Fórmula empírica (notación de Hill): C₃₁H₃₃N₃O₁₀
• Número de CAS: 150571-28-1
• Peso molecular: 607.61
• Número MDL: MFCD08064317
• Código UNSPSC: 12352209
• NACRES: NA.22

Propiedades

• Nivel de calidad: 100
• Ensayo: ≥98%
• Formulario: powder
• mp: 108 °C (decomp.)
• temp. de almacenamiento: 2-8°C
• cadena SMILES: [N+](=O)([O-])c1c(cc(c(c1)OC)OC)COC(=O)NCCCC[C@H](NC(=O)OCC2c3c(cccc3)c4c2cccc4)C(=O)O
• InChI: 1S/C31H33N3O10/c1-41-27-15-19(26(34(39)40)16-28(27)42-2)17-43-30(37)32-14-8-7-13-25(29(35)36)33-31(38)44-18-24-22-11-5-3-9-20(22)21-10-4-6-12-23(21)24/h3-6,9-12,15-16,24-25H,7-8,13-14,17-18H2,1-2H3,(H,32,37)(H,33,38)(H,35,36)/t25-/m0/s1
• Clave InChI: UOEGMVQGRMCJDM-VWLOTQADSA-N

Descripción

Aplicación

Fmoc-L-Lys(Nvoc)-OH is a lysine derivative compatible with solid-phase peptide synthesis (SPPS). The photolabile, N-terminal protecting group nitroveratryloxycarbonyl (NVOC) can be cleaved by photolysis at 350 nm. Photocaged amino acids such as these are useful in the synthesis of photocleavable chemical tools for spatial and temporal control over released molecules in biological applications.

Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)

Otras notas

Total chemical synthesis of photoactivatable proteins for light-controlled manipulation of antigen-antibody interactions

In situ cell manipulation through enzymatic hydrogel photopatterning

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable