Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Ernesto Santandrea"'
Autor:
Jialei Gu, Yingtao Tian, Xingmin Zhang, Marian Lanz, Pascale Hoehn, Luisa Heinz, Ernesto Santandrea, Guido Jordine, Xigui Jiang, Hao Zhang, Liangxing Wang, Chongfeng Pan, Fengfeng Guo, Jialiang Li
Publikováno v:
Organic Process Research & Development. 26:2908-2914
Publikováno v:
Organic Process Research & Development. 25:1190-1205
The development of the late-phase manufacturing process of the drug candidate ZPL389 and the strategies for the control of impurities are outlined in detail. Selective salt formation at several sta...
Autor:
Ralf Jockers, Nicola Antonio Colabufo, Anna Floriana Sciarroni, Ferdinando Maria Milazzo, Paola Vitale, Ernesto Santandrea, Laura Bleve, Antonio Scilimati, Maria Grazia Perrone
Publikováno v:
Bioorganic & Medicinal Chemistry. 16:2473-2488
Since it is widely distributed into the body, beta(3)-adrenoceptor is becoming an attractive target for the treatment of several pathologies such as obesity, type 2 diabetes, metabolic syndrome, cachexia, overactive bladder, ulcero-inflammatory disor
Publikováno v:
Advanced Synthesis & Catalysis. 349:1111-1118
A yeast alcohol dehydrogenase (ADH) has been purified up to a purification factor value of 21,731-fold from Kluyveromyces marxianus CBS 6556. The purification procedure consisted of two chromatographic steps (DEAE-anion exchange and affinity chromato
Autor:
Antonio Scilimati, Ernesto Santandrea, Paolo Tortorella, Laura Bleve, Erika Giorgio, Maria Grazia Perrone
Publikováno v:
Bioorganic & Medicinal Chemistry. 14:1207-1214
Enantiomerically pure (R)-2-chloro-1-(pyridin-3-yl)ethanol has been prepared by kinetic resolution performed in the presence of Candida antarctica SP435-L lipase immobilized on a macroporous polyacrylate resin (Novozym 435®). It was converted into (
Autor:
Antonio Scilimati, Vincenzo Tortorella, Ernesto Santandrea, Christoph Syldatk, Maria Grazia Perrone
Publikováno v:
Tetrahedron: Asymmetry. 16:1473-1477
Reduction of oxoesters 1b – d and 1f , g in the presence of different yeast strains ( Saccharomyces cerevisiae DSM 11285, S. cerevisiae CBS 7336, Cryptococcus curvatus ATCC 20509, Candida bombicola ATCC 22214, Trigonopsis variabilis DSM 70714, Kluy
Autor:
Maria Grazia Perrone, Fabio Giannessi, Natalina Dell'uomo, Ernesto Santandrea, Anna Floriana Sciarroni, Ferdinando Maria Milazzo, Vincenzo Tortorella, Antonio Scilimati
Publikováno v:
European Journal of Medicinal Chemistry. 40:143-154
Clofibrate is a lipid-profile modifying agent belonging to the fibrate class of drugs. Fibrates are known to exhibit their beneficial effects by activating peroxisome proliferator-activated receptor-α (PPARα) and used in the treatment of dyslipidem
Autor:
Ernesto Santandrea, Christoph Syldatk, Valerio Bertolasi, Francesco Capitelli, Vincenzo Tortorella, Maria Grazia Perrone, Antonio Scilimati
Publikováno v:
Tetrahedron: asymmetry
15 (2004): 3511–3517. doi:10.1016/j.tetasy.2004.08.028
info:cnr-pdr/source/autori:Perrone M.G. 1, Santandrea E. 1, Scilimati A. 1, Syldatk C. 2, Tortorella V. 1, Capitelli F. 3, Bertolasi V. 4/titolo:Diastero-and enantioselective bioreduction of ethyl 2-(4-chlophenoxy)-3-oxobutanoate clofibrate analogues by Kluyveromyces marxianus and other whole cell biocatalysts/doi:10.1016%2Fj.tetasy.2004.08.028/rivista:Tetrahedron: asymmetry (Print)/anno:2004/pagina_da:3511/pagina_a:3517/intervallo_pagine:3511–3517/volume:15
15 (2004): 3511–3517. doi:10.1016/j.tetasy.2004.08.028
info:cnr-pdr/source/autori:Perrone M.G. 1, Santandrea E. 1, Scilimati A. 1, Syldatk C. 2, Tortorella V. 1, Capitelli F. 3, Bertolasi V. 4/titolo:Diastero-and enantioselective bioreduction of ethyl 2-(4-chlophenoxy)-3-oxobutanoate clofibrate analogues by Kluyveromyces marxianus and other whole cell biocatalysts/doi:10.1016%2Fj.tetasy.2004.08.028/rivista:Tetrahedron: asymmetry (Print)/anno:2004/pagina_da:3511/pagina_a:3517/intervallo_pagine:3511–3517/volume:15
Growing and resting cells of several yeasts, which catalyze the hydride transfer to a carbonyl, were screened and used in conditions to find out the suitable methodology to prepare clofibrate analogues. Clofibrate is an antilipidemic drug. In particu
Autor:
Paola Vitale, Ernesto Santandrea, Maria Grazia Perrone, Mauro Niso, Laura Bleve, Antonio Scilimati
Publikováno v:
ChemMedChem. 4(12)
Novel compounds were prepared in fair to good yields as human beta(3)-adrenoceptor (beta(3)-AR) agonists. In particular, aryloxypropanolamines 7 a-d (EC(50)=0.57-2.1 nM) and arylethanolamines 12 a,b,e (EC(50)=6.38-19.4 nM) were designed to explore th
Autor:
Anna Floriana Sciarroni, Maria Grazia Perrone, Antonio Scilimati, Natalina Dell'uomo, Ferdinando Maria Milazzo, Fabio Giannessi, Vincenzo Tortorella, Ernesto Santandrea
Publikováno v:
ChemInform. 36
Clofibrate is a lipid-profile modifying agent belonging to the fibrate class of drugs. Fibrates are known to exhibit their beneficial effects by activating peroxisome proliferator-activated receptor-α (PPARα) and used in the treatment of dyslipidem