Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Juho Hokkanen"'
Publikováno v:
Frontiers in Pharmacology, Vol 1 (2010)
Liquid chromatography-mass spectrometry (LC/MS) with generic gradient elution for a large number of chemically different compounds is a common approach in drug development, used to acquire a large amount of data in a short time frame for drug candida
Externí odkaz:
https://doaj.org/article/5d7b104c8e164552bc435f534e53ff33
Autor:
Juho Hokkanen, Maxi Heyner, Juana Díez, Valtteri Rinne, Mark Brönstrup, Kirsten Harmrolfs, Yuichi Sugiyama, Katharina Rox, Rolf Müller, Andrea Kröger, Jana Krull, Gemma Perez Vilaro
Publikováno v:
ACS Pharmacol Transl Sci
[Image: see text] While a drug treatment is unavailable, the global incidence of Dengue virus (DENV) infections and its associated severe manifestations continues to rise. We report the construction of the first physiologically based pharmacokinetic/
Autor:
Juho Hokkanen, Olayemi M. Adegbolagun, Titilayo O. Fakeye, Ari Tolonen, Sharon I. Igbinoba, Marena Kajula, Johnson Segun Showande
Publikováno v:
Journal of Basic and Clinical Physiology and Pharmacology. 30
Background Hibiscus sabdariffa beverage (HSB) is widely consumed as a medicinal herb and sometimes used concomitantly with drugs. This study evaluated the in vitro inhibitory potential of the aqueous extract of H. sabdariffa calyces (AEHS) on selecte
Autor:
Hans-Georg Sahl, Pere Picart, Ari Turpeinen, Marena Kajula, Janne A. Ihalainen, Mysore V. Tejesvi, Anna Maria Pirttilä, Sampo Mattila, Ari Tolonen, Juho Hokkanen, Joshua M. Ward, Heikki Häkkänen
Publikováno v:
Journal of Natural Products. 79:685-690
Three new epithiodiketopiperazine natural products [outovirin A (1), outovirin B (2), and outovirin C (3)] resembling the antifungal natural product gliovirin have been identified in extracts of Penicillium raciborskii, an endophytic fungus isolated
Autor:
Juho Hokkanen, John Z. Cao, Tuukka Ihantola, William G. Kaelin, Christopher J. Mariani, Lucy A. Godley, Peppi Koivunen, Tuomas Laukka
Publikováno v:
Journal of Biological Chemistry. 291:4256-4265
The TET enzymes are members of the 2-oxoglutarate-dependent dioxygenase family and comprise three isoenzymes in humans: TETs 1-3. These TETs convert 5-methylcytosine to 5-hydroxymethylcytosine (5-hmC) in DNA, and high 5-hmC levels are associated with
Publikováno v:
Food Science & Nutrition, 7(1):44-55
Food Science & Nutrition
Food Science & Nutrition
Background Increasing use of medicinal herbs as nutritional supplements and traditional medicines for the treatment of diabetes, hypertension, hyperlipidemia, and malaria fever with conventional drugs poses possibilities of herb–drug interactions (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::302c07650a5664eb27d7850d8454e576
Wiley Online Library
Wiley Online Library
Publikováno v:
Chemical Research in Toxicology. 28:2292-2303
Many carboxylic acid-containing drugs are associated with idiosyncratic drug toxicity (IDT), which may be caused by reactive acyl glucuronide metabolites. The rate of acyl migration has been earlier suggested as a predictor of acyl glucuronide reacti
Publikováno v:
Journal of Agricultural and Food Chemistry. 57:9437-9447
Phenolic compounds from leaves of lingonberry (Vaccinium vitis-idaea L.), bilberry (Vaccinium myrtillus L.), and the natural hybrid of bilberry and lingonberry (Vaccinium x intermedium Ruthe L., hybrid bilberry) were identified using LC/TOF-MS and LC
Autor:
Sampo Mattila, Anja Hohtola, Ari Tolonen, Anna Maria Pirttilä, Juho Hokkanen, Janne J. Koskimäki, Laura Jaakola, Marja Suorsa
Publikováno v:
European Journal of Plant Pathology. 125:629-640
Bilberry (Vaccinium myrtillus) represents one of the richest flavonoid sources among plants. Flavonoids play variable, species-dependent roles in plant defences. In bilberry, flavonoid metabolism is activated in response to solar radiation but not ag
Publikováno v:
FEBS Journal. 275:4329-4342
Hypericins are biologically active constituents of Hypericum perforatum (St John's wort). It is likely that emodin anthrone, an anthraquinone precursor of hypericins, is biosynthesized via the polyketide pathway by type III polyketide synthase (PKS).