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78485

Sigma-Aldrich

N,N′-(1,4-Phenylene)dimaleimide

≥98.0% (HPLC)

Sinônimo(s):

1,4-Dimaleimidobenzene, N,N′-(p-Phenylene)dimaleimide

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About This Item

Fórmula empírica (Notação de Hill):
C14H8N2O4
Número CAS:
3278-31-7
Peso molecular:
268.22
Beilstein:
249631
Número CE:
221-910-6
Número MDL:
MFCD00005505
Código UNSPSC:
12162002
ID de substância PubChem:
24887314

Ensaio

≥98.0% (HPLC)

pf

>300 °C (lit.)

cadeia de caracteres SMILES

O=C1C=CC(=O)N1c2ccc(cc2)N3C(=O)C=CC3=O

InChI

1S/C14H8N2O4/c17-11-5-6-12(18)15(11)9-1-2-10(4-3-9)16-13(19)7-8-14(16)20/h1-8H

chave InChI

AQGZJQNZNONGKY-UHFFFAOYSA-N

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Outras notas

Bifunctional thiol reagent for the cross-linking of proteins; Efficient procedure for the conjugation of an antibody with an enzyme

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S Yoshitake et al.
Scandinavian journal of immunology, 10(1), 81-86 (1979-01-01)
An efficient procedure for the conjugation of rabbit Fab' with beta-D-galactosidase from Escherichia coli using N,N-o-phenylenedimaleimide is described. Thiol groups of Fab' were stabilized by the presence of ethylenediaminetetraacetate, and malemide groups were shown to be stable at pH 5
P Knight
The Biochemical journal, 179(1), 191-197 (1979-04-01)
To understand the extent of the cross-linking of proteins by the bifunctional reagent p-NN'-phenylenebismaleimide, a quantitative study of competing reactions has been undertaken. The two reactive maleimide rings of the bismaleimide are hydrolysed in mildly alkaline aqueous solutions much more
P Knight et al.
Biochemistry, 19(20), 4682-4687 (1980-09-30)
The hypothesis that the subunits of F-actin rotate during interactin with myosin and ATP has been tested by using the specific cross-linking reagent p-phenylene-N,N'-bis(maleimide) (PM). The insertion of cross-links between F-actin subunits does not change the ability of the F-actin
J A Wells et al.
Proceedings of the National Academy of Sciences of the United States of America, 76(10), 4966-4970 (1979-10-01)
Studies with reagents that crosslink two thiol groups have shown that it is possible to trap nucleotides at the active site of myosin chymotryptic subfragment 1. Subfragment 1 incorporates nearly stoichiometric quantities of [14C]ATP or [14C]ADP in a manner that

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