Zobrazeno 1 - 10
of 48
pro vyhledávání: '"D J Buurman"'
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0208922 (2018)
IntroductionTNF-α-neutralizing antibodies, such as infliximab (IFX) and adalimumab (ADA), are effective in the treatment of inflammatory bowel diseases (IBD), but they are expensive and become ineffective when patients develop anti-IFX or anti-ADA a
Externí odkaz:
https://doaj.org/article/ee266d4620e84cd8b0bd9a322485b04a
Autor:
Elisabeth Brouwer, Eleonora A. M. Festen, Tjasso Blokzijl, Klaas Nico Faber, B T Pham, Gerard Dijkstra, D. J. Buurman
Publikováno v:
PLoS ONE, 13(12):0208922. PUBLIC LIBRARY SCIENCE
PLoS ONE, Vol 13, Iss 12, p e0208922 (2018)
PLoS ONE
PLoS ONE, Vol 13, Iss 12, p e0208922 (2018)
PLoS ONE
IntroductionTNF-alpha-neutralizing antibodies, such as infliximab (IFX) and adalimumab (ADA), are effective in the treatment of inflammatory bowel diseases (IBD), but they are expensive and become ineffective when patients develop anti-IFX or anti-AD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb120f7a3c4aa9a260892a9c95c65751
https://research.rug.nl/en/publications/9ab36a6e-d90f-4dc9-9b99-b03ba0c0a96f
https://research.rug.nl/en/publications/9ab36a6e-d90f-4dc9-9b99-b03ba0c0a96f
Autor:
D. J. Buurman, H. J. den Hertog
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 91:841-849
The isomeric aminobromoquinolines in which amino groups and bromine atoms are attached to the pyridine nucleus were reacted with potassium amide in liquid ammonia at −33°. 2-Amino-3-bromo- and 2-amino-4-bromo-quinoline are converted via 3,4-didehy
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 80:325-329
The reaction mixture formed during the heating of pyridine-N-oxide with p-toluenesulphonyl chloride contains, together with pyridine, 2,3′-dipyridyl ether, 3-pyridyl p-toluenesulphonate and N-(2Prime;-pyridyl)-pyridone-2 two chloro compounds, viz.
Autor:
D. J. Buurman, H. J. den Hertog
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 92:304-310
Aminations of 2,3-, 2,4- and 3,4-dibromoquinoline with potassium amide in different media have been investigated. Reactions of various types (bromine migration, dimerization, cine-substitutions and various ring transformations) were found to occur. M
Publikováno v:
Recueil des travaux chimiques des Pays-Bas = Journal of the Royal Netherlands Chemical Society, 101, 342-346
Recueil des travaux chimiques des Pays-Bas = Journal of the Royal Netherlands Chemical Society 101 (1982)
Recueil des travaux chimiques des Pays-Bas = Journal of the Royal Netherlands Chemical Society 101 (1982)
A method is described for the oxidation of some 1-alkyl-3-carbamoylpyridinium chlorides by reaction with immobilized rabbit liver aldehyde oxidase. With the 1-methyl-, 1-ethyl-and 1-n-propyl derivatives, only the 1-alkyl-1,6-dihydro-6-oxo-3-pyridinec
Autor:
H. J. den Hertog, D. J. Buurman
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 75:257-264
Syntheses of 2-hydroxy-4-methoxypyridine, 4-hydroxy-2-methoxypyridine, 4-methoxy-N-methylpyridone-2, and 2-methoxy-N-methylpyridone-4 are described. The ultraviolet absorption spectra of 50% aqueous ethanolic solutions of the above-mentioned compound
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 77:963-971
When pyridine is heated with 100% sulphuric acid in the presence of mercuric sulphate as a catalyst at about 275°, pyridine-3-sulphonic acid is formed as the chief product, together with very small amounts of byproducts. The course of the reaction i
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 102:331-336
Oxidation of 1-aryl-3-carbamoylpyridinium chlorides with immobilized rabbit liver aldehyde oxidase gave predominantly 1-aryl-1,6-dihydro-6-oxo-3-pyridinecarboxamides, together with the corresponding 1-aryl-1,4-dihydro-4-oxo-3-pyridinecarboxamides. In
Autor:
H. J. den Hertog, D. J. Buurman
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 86:187-192
Both 3- and 4-bromoquinoline when reacted with potassium amide in liquid ammonia, are converted into a mixture of 3- and 4-aminoquinoline probably via 3,4-quinolyne as an intermediate. 2-Bromoquinoline yields together with 2-aminoquinoline, 2-methylq