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pro vyhledávání: '"C. Nerenberg"'
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Akademický článek
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Publikováno v:
Pharmaceutical research. 3(2)
A procedure is described that is suitable for the radioimmunoassay (RIA) of 9-[(l,3-dihydroxy-2-propoxy)-methyl]guanine (DHPG) in plasma or serum at concentrations as low as 0.7 ng/ml (2.75 × 10(-9) M). Antiserum was prepared by coupling DHPG monohe
Publikováno v:
Journal of Immunoassay. 9:245-255
A procedure for the radioimmunoassay (RIA) of detirelix in plasma or serum at concentrations as low as 0.15 ng/ml is described. Antiserum was produced by deacetylation of the N-terminus amino groups of detirelix and coupling this analog to bovine ser
Publikováno v:
Canadian Journal of Chemistry. 40:133-142
The preparation of 3,4-methylenedioxy-α-aminomethylbenzyl alcohol and a number of its N-alkyl and N,N-dialkyl derivatives by the reduction or reductive alkylation of 3,4-methylenedioxy-α-nitromethylbenzyl alcohol is described.
Autor:
C. Nerenberg, Roland Fischer
Publikováno v:
Stain Technology. 38:75-84
Column and paper chromatography of four thiazin dyes revealed both inorganic and organic impurities. In thionin, azure A, azure B and methylene blue, sodium and other metal cations were found as inorganic impurities. The analysis for organic impuriti
Publikováno v:
Canadian Journal of Chemistry. 39:1143-1147
not available
Publikováno v:
Canadian Journal of Chemistry. 36:853-857
The preparation of adrenochrome in a pure stable crystalline form has been carried out by the silver oxide oxidation of adrenaline in methanol with the use of an anion-exchange resin (Dowex-1(Cl−)) to remove heavy metal ions from the reaction mixtu
Autor:
C. Nerenberg, S.B. Matin
Publikováno v:
Journal of pharmaceutical sciences. 70(8)
A simple radioimmunoassay was developed for the measurement of flunisolide in human plasma or serum. Plasma extraction was not required. Antiserums were produced in rabbits by immunization against the flunisolide 21-hemisuccinate-bovine serum albumin
Publikováno v:
LHRH and Its Analogs ISBN: 9789401089630
The delivery of polypeptide and protein drugs by a convenient and effective method is a major challenge in the development of these compounds as therapeutic agents. Due to degradation and/or lack of absorption in the gastrointestinal tract, large, un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55a63046129f0cecb73b2412c2ea96d8
https://doi.org/10.1007/978-94-009-5588-2_33
https://doi.org/10.1007/978-94-009-5588-2_33