Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Hans-Georg Häcker"'
Autor:
Claudia Vicente Martin, Stephan Stocker, Manel Bautista, Vincent Rogue, Caroline Steib-Lauer, Hans-Georg Häcker, Dirk Spickermann, Stefan Hirsch, Sundeep S. Dhareshwar
Publikováno v:
Drug Development and Industrial Pharmacy. 48:211-225
This work summarizes select methodology of twin-screw melt granulation (TSMG) and process analytical technology that were used in the successful scaling-up and commercial transfer of high drug load (80.5% w/w) immediate release fevipiprant tablets.Th
Autor:
Antje de la Haye, Michael Gütschow, Katja Sterz, Michael Wiese, Hans-Georg Häcker, Gregor Schnakenburg
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 19:6102-6105
P-glycoprotein (P-gp) is an important factor in the development of multidrug resistance (MDR) in cancer cells. In literature reports, a thieno[2,3-d]pyrimidine (QB13) was described as P-gp modulator and opposed effects on the cell accumulation of dis
Autor:
Gregor Schnakenburg, Markus Pietsch, Wilfried Hoffbauer, Hans-Georg Häcker, Michael Gütschow, Jörg Daniels
Publikováno v:
Journal of Molecular Structure. 934:23-27
The normal acid salt isopropylammonium tetrafluorohydrogenphthalate (3) was prepared and its structure was determined by X-ray crystallography. This salt is stabilized by N–H…O, O–H…O, C–H…O, and N–H…F hydrogen bonds. Compound 3 was c
Autor:
Susanne Michels, Michael Gütschow, Paul W. Elsinghorst, Jörg Daniels, Hans-Georg Häcker, Gregor Schnakenburg
Publikováno v:
Synthesis. 2009:1195-1203
The reactions of N-benzoyl-N'-(o-cyanoaryl)thioureas with ethyl bromoacetate under alkaline conditions led to the formation of either fused 2-(alkylsulfanyl)-4-aminopyrimidines or 2-(benzoylimino)-3-(o-cyanoaryl)thiazolidin-4-ones. The accurate appli
Autor:
Markus Pietsch, Gregor Schnakenburg, Michael Gütschow, Wilfried Hoffbauer, Hans-Georg Häcker, Martin Nieger
Publikováno v:
Journal of Molecular Structure. 878:131-138
An anomalous acid salt ( 2 ) in the 2:1 ratio of tetrafluorophthalic acid and isopropylamine was prepared from bis(isopropylammonium) tetrafluorophthalate ( 1 ). Both salts were characterized by 13 C NMR spectroscopy in solution and in solid state, a
Publikováno v:
Int. Journal of Clinical Pharmacology and Therapeutics. 48:445-447
Autor:
Paul W. Elsinghorst, Gregor Schnakenburg, Hans-Georg Häcker, Philipp A. Ottersbach, Michael Gütschow
Publikováno v:
Tetrahedron Letters. 51:2727-2729
The reaction of isatoic anhydride (1) with carbon disulfide at room temperature unexpectedly afforded 1,2-dihydro-2-thioxo-4H-3,1-benzothiazin-4-one (2). The use of 13C-labeled carbon disulfide elucidated that CS2 was entirely incorporated into the p
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 18:4761-4763
We present a novel lead for inhibitors of multidrug resistance-associated proteins (MRPs). Compound 1 (4-[(5,6,7,8-tetrahydro-4-oxo-4H-[1]benzothieno[2,3-d][1,3]thiazin-2-yl)amino]benzoic acid) was about six times more potent than the known inhibitor
Publikováno v:
Pharmacologytherapeutics. 132(2)
Caspases are proteolytic enzymes mainly involved in the induction and execution phases of apoptosis. This type of programmed cell death is an essential regulatory process required to maintain the integrity and homeostasis of multicellular organisms.
Publikováno v:
ACS combinatorial science. 13(1)
Acylureas (ureides) are valued for their important biological activities. Whereas cyclic acylureas have frequently been the object of solid-phase chemistry, only few reports have focused on the solid-supported preparation of acyclic representatives.