Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Per Strande"'
1
Starch microspheres as carriers for X-ray imaging contrast agents: Synthesis and stability of new amino-acid linker derivatives
Autor: Jo Klaveness, Pal Rongved, Per Strande
Publikováno v: Carbohydrate Research. 297:325-331
The relative stability of particulate contrast agents for X-ray imaging, consisting of a succinic-acid derivative of a water-soluble X-ray contrast agent bound to starch particles through an amino-acid ester bond, has been studied. To investigate the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::560d93355d4d8aafe1d1f5be2376be15
https://doi.org/10.1016/s0008-6215(96)00286-8
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2
Polysaccharides as carriers for magnetic resonance imaging contrast agents: Synthesis and stability of a new amino acid linker derivative
Autor: Pal Rongved, Per Strande, Tone Hauk Fritzell, Jo Klaveness
Publikováno v: Carbohydrate Research. 287:77-89
The relative hydrolytic stability of contrast agents for magnetic resonance imaging (MRI), consisting of paramagnetic metal chelates bound to polysaccharides through an ester bond, has been investigated. Four preparations of biodegradable, cross-link
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0cbdb91d3d1ef70e6511d7d333cf0767
https://doi.org/10.1016/0008-6215(96)00062-6
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3
Pyrimidinones as reversible metaphase arresting agents
Autor: Reidar Oftebro, Per Strande, Tore Benneche, Kjell Undheim
Publikováno v: European Journal of Medicinal Chemistry. 28:463-472
5-Halo- N (1)-substituted 2(1 H )-pyrimidinones have the ability to cause reversible arrest of mitosis during metaphase. Highly active compounds have a heteroatom ( O , S or N ) in the β-position of the N (1)-carbon chain which is further substitute
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9989cd232673e71882e11dc54d43d1c9
https://doi.org/10.1016/0223-5234(93)90014-6
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8
Crystal and molecular structures of the isomeric dipeptides alpha-L-aspartyl-L-alanine and beta-L-aspartyl-L-alanine
Autor: C. H. Görbitz, Per Strande, Kjell Undheim, Robert W. Taft, G. W. Fischer
Publikováno v: Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry. 41(9)
The crystal and molecular structures of the alpha- and beta-L-Asp isomers of L-aspartyl-L-alanine have been determined at 120 K using 1226 and 1609 reflections (I greater than 2.5 sigma I), respectively. The space group for the alpha-isomer is P2(1),
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76816c21b2e80fe168b0b8752b13d87e
https://pubmed.ncbi.nlm.nih.gov/3442178
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