Mal-L-Dap(Boc)-OH*DCHA

Nombre químico: N-alpha-MaleimidoN-beta-t-butyloxycarbonyl-L-2,3-diaminopropionic acid dicyclohexylamine // Sinónimos: Mal-Dap(Boc)*DCHA, Mal-Dpr(Boc)*DCHA CAS 1491152-23-8 net, Mal-Dap(Boc)-OH*DCHA

  • Nº Artículo:MAA1040
  • Nº CAS:2004724-16-5
  • Fórmula:C12H16N2O6*C12H23N
  • Storage temperature:2-8°C
  • Masa molecular:284,27*181,32 g/mol
  • Pureza:min. 99%
  • Pureza Enantiomérica:min. 99,7%

from 80,00 €

Grouped product items
Cantidad Unidad de venta Precio Unidad de almacenamiento de stock (SKU) Disponibilidad
250 mg
80,00 €
MAA1040.0250
<10 días laborables
500 mg
144,00 €
MAA1040.0500
<10 días laborables
1 g
224,00 €
MAA1040.0001
<10 días laborables
5 g
800,00 €
MAA1040.0005
<10 días laborables
25 g
3.200,00 €
MAA1040.0025
<10 días laborables
Hoja de seguridad
description

Building block, which can be used for conjugation with thiol groups. After removal of the Boc protecting group and conjugation with the mercaptane function the free methylamino side chain will open the maleimide ring under aqueous conditions. While the conjugation reaction between thiol and maleimid is reversible, it turns completely stable in the open ring structure. This becomes particularly important in the formation of conjugates with high value components, like in antibody-drug conjugation (ADC).

references

Self-hydrolyzing maleimides improve the stability and pharmacological properties of antibody-drug conjugates; R.P. Lyon, J.R. Setter, T.D. Bovee, S.O. Doronia, J.H. Hunter, M.E.

Anderson, C.L.Balasubramanian, S.M. Duniho, C.I. Leiske, F. Li, P.D. Senter; Nature Biotechnology. 2014; 32(10): 1059-1062. Doi:10.1038/nbt.2968.

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