Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Juha Juntunen"'
Autor:
Keijo Koski, Matti Sarkimo, Juha Juntunen, Kari Lahdenperä, Sauli Liukkonen, Aslak Siljander, Jarkko Tikka, Mika Bäckström, R. Lahtinen
Publikováno v:
Koski, K, Siljander, A, Bäckström, M, Liukkonen, S, Juntunen, J, Sarkimo, M, Lahdenperä, K, Tikka, J & Lahtinen, R 2009, ' Fatigue, residual strength and non-destructive tests of an aging aircraft's wing detail ', International Journal of Fatigue, vol. 31, no. 6, pp. 1089-1094 . https://doi.org/10.1016/j.ijfatigue.2008.05.015
This study concentrates on fatigue, residual strength and non-destructive tests of an aging aircraft’s wing detail of the Finnish Air Force’s Hawk Mk.51 jet trainer. The studied detail was the integral stiffener with a drain hole near the wing ro
Autor:
Karen Ulmer, Kenneth B. Sloan, Surjit Singh, Hema Devarajan, Donna Nickels, Scott Wasdo, Juha Juntunen, Thomas L. Murray, Thea Shanks
Publikováno v:
European Journal of Pharmaceutical Sciences. 34:321-332
Do the Roberts–Sloan (RS) or modified Kasting–Smith–Cooper (KSC) equations that provide good fit to data for maximum flux, from water through mouse or human skin also provide a good fit to data for maximum fluxes through silicone membranes (pol
Publikováno v:
International Journal of Pharmaceutics. 351:92-103
A database ( n = 50) consisting of values of solubility in water, S AQ , solubility in octanol, S OCT , molecular weight, MW, and maximum flux based on the delivery of total species containing a parent drug by its prodrugs through human skin in vitro
Autor:
Erik A.A. Wallén, Johannes A. M. Christiaans, Pekka T. Männistö, Jarkko I. Venäläinen, Elina M. Jarho, Tomi Järvinen, Juha Juntunen, Markus M. Forsberg, A. Leena Yli-Kokko, Jouko Vepsäläinen
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 16:5590-5593
A series of ionizable prolyl oligopeptidase inhibitors were developed through the introduction of a pyridyl group to the P3 position of the prolyl oligopeptidase inhibitor structure. The study was performed on previously developed prolyl oligopeptida
Autor:
Juha Juntunen, Tapio Nevalainen, Juhani Huuskonen, Krista Laine, Riku Niemi, David W. Pate, Hannu Taipale, Tomi Järvinen
Publikováno v:
European Journal of Pharmaceutical Sciences. 19:37-43
Phosphate esters of arachidonylethanolamide (AEA) and R-methanandamide were synthesized and evaluated as water-soluble prodrugs. Various physicochemical properties (pKa, partition coefficient, aqueous solubility) were determined for the synthesized p
Autor:
Kenneth B. Sloan, Juha Juntunen, Susruta Majumdar, Maren Mueller Spaeth, Joshua D. Thomas, Sashikala Sivendran
Publikováno v:
Tetrahedron Letters. 48:4609-4611
Synthesis of α-(1H-imidazol-1-yl)alkyl (IMIDA) carboxylic acid esters have been reported in 2–3 simple steps. α-(1H-Imidazol-1-yl)alkyl (IMIDA) carboxylic acid esters were found to be chemically labile and thus serve as novel prodrugs of carboxyl
Publikováno v:
The Journal of pharmacy and pharmacology. 57(9)
Topically administered cannabinoids have been shown to reduce intraocular pressure by interacting with the ocular cannabinoid receptor. Most cannabinoids have very poor aqueous solubility, which limits their pharmaceutical development and usefulness.
Publikováno v:
Journal of medicinal chemistry. 46(23)
The poor aqueous solubility of 2-arachidonyl glyceryl ether (noladin ether) 2 hinders both pharmacological studies and pharmaceutical development. The synthesized mono- and diphosphate esters of noladin ether (4 and 6) considerably increased the aque
Autor:
Séverine Vandevoorde, Kent-Olov Jonsson, Jeffrey C. Jerman, Darren Smart, Didier M. Lambert, Tomi Järvinen, Anna Andersson, Christopher J. Fowler, Juha Juntunen
Publikováno v:
Biochemical pharmacology. 66(5)
It has previously been shown that the endocannabinoids anandamide and 2-arachidonoylglycerol (2-AG) inhibit the proliferation of C6 glioma cells in a manner that can be prevented by a combination of capsazepine (Caps) and cannabinoid (CB) receptor an
Autor:
Juha, Juntunen, Juhani, Huuskonen, Krista, Laine, Riku, Niemi, Hannu, Taipale, Tapio, Nevalainen, David W, Pate, Tomi, Järvinen
Publikováno v:
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences. 19(1)
Phosphate esters of arachidonylethanolamide (AEA) and R-methanandamide were synthesized and evaluated as water-soluble prodrugs. Various physicochemical properties (pK(a), partition coefficient, aqueous solubility) were determined for the synthesized