Results 21 to 30 of about 229,143 (305)

Kajian Farmakoinformatika Senyawa Alkaloid Anggur Laut (Caulerpa racemose) Sebagai Inhibitor Collagenase Dalam Mekanisme Antiaging

open access: yesFlorea: Jurnal Biologi dan Pembelajarannya, 2022
Caulerpa racemosa or sea grape is an edible macroalgae, cultivated and wild species in Asia ocean. Sea grapes also well known as functional food source from marine, contains high protein, fibers and secondari metabolites.
Dewi Ratih Tirto Sari   +2 more
doaj   +1 more source

Detection of substrate binding motifs for morphine biosynthetic pathway intermediates in novel wound inducible (R,S)-reticuline 7-O-methyltransferase of Papaver somniferum [PDF]

open access: yes, 2011
The benzylisoquinoline alkaloids (BIA) comprise a large and diverse group of nitrogen-containing secondary metabolites with about 2500 compounds identified in plants.
Abha Meena   +5 more
core   +2 more sources

Validation of analytical method for determination of microbiological quality of antifungal shampoo containing 2% ketoconazole: Enumeration test and tests for specified microorganisms (Method suitability test) [PDF]

open access: yesMakedonsko Farmacevtski Bilten
Microbiological quality screening of non - sterile product is conducted by suitable enumeration tests and tests for absence of specified microorganisms. The European Pharmacopoeia offers several methods for conducting these tests.
Nadica Gjurichikj   +5 more
doaj   +1 more source

Fast and selective HPLC-DAD method for determination of pholcodine and related substances

open access: yesMacedonian Journal of Chemistry and Chemical Engineering, 2011
Quality control of pharmaceuticals requires development of fast, efficient and reliable methods for determination of active compounds as well as known and very often unknown impurities within defined concentration ranges. In this work, a simple and rapid
Ana Petkovska   +2 more
doaj   +1 more source

Pd-catalyzed enantioselective aerobic oxidation of secondary alcohols: Applications to the total synthesis of alkaloids [PDF]

open access: yes, 2008
Enantioselective syntheses of the alkaloids (-)-aurantioclavine, (+)-amurensinine, (-)-lobeline, and (-)- and (+)-sedamine are described. The syntheses demonstrate the effectiveness of the Pd-catalyzed asymmetric oxidation of secondary alcohols in ...
Bagdanoff, Jeffrey T.   +5 more
core   +2 more sources

Piperine Reduces Neoplastic Progression in Cervical Cancer Cells by Downregulating the Cyclooxygenase 2 Pathway

open access: yesPharmaceuticals, 2023
Cervical cancer is the fourth-most common type of cancer in the world that causes death in women. It is mainly caused by persistent infection by human papillomavirus (HPV) that triggers a chronic inflammatory process.
Luana Pereira Cardoso   +8 more
doaj   +1 more source

Total Synthesis and Structural Revision of the Alkaloid Incargranine B [PDF]

open access: yes, 2013
Seeing double: Consideration of the biosynthetic origins of incargranineB, which was originally assigned an unprecedented indolo[1.7]naphthyridine structure, led to the proposal of a dipyrroloquinoline framework as a more biosynthetically feasible ...
Bates   +8 more
core   +1 more source

Validacija na metod za opredeluvanje mikrobioloska cistota na Kafetin® tableti [PDF]

open access: yesMakedonsko Farmacevtski Bilten, 2003
Izvrsena e validacija na metodot za opredeluvawe mikrobioloska cistota na Kafetin® tableti. Za taa cel koristeni se test-mikroorganizmi: Escherichia coli, Pseudomonas aeruginosa ,Staphylococcus aureus, Candida albicans i Aspergillus niger, od ...
Dragi Todorovik   +2 more
doaj  

Network-analysis-guided synthesis of weisaconitine D and liljestrandinine. [PDF]

open access: yes, 2015
General strategies for the chemical synthesis of organic compounds, especially of architecturally complex natural products, are not easily identified. Here we present a method to establish a strategy for such syntheses, which uses network analysis.
Gallego, GM   +8 more
core   +2 more sources

Novel pyrrolizidine alkaloid [PDF]

open access: yes, 1991
The present invention involves a purified bioactive compound of the formula: ##STR1## wherein at least one of R.sub.1, R.sub.2, R.sub.3 and R.sub.4 are H or an acyl having less than about five carbon atoms.
Elbein, Alan D., Tropea, Joseph E.
core   +1 more source

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