Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Irene Kylänlahti"'
Autor:
Virpi Talman, Heinrich Lang, Jari Yli-Kauhaluoma, Irene Kylänlahti, Raimo K. Tuominen, Henri Xhaard, Elina Ekokoski, Timo Ruotsalainen, Gustav Boije af Gennäs, Tobias Rüffer, Gloria Wissel, Alexandros Kiriazis
Publikováno v:
Tetrahedron. 67:8665-8670
Protein kinase C (PKC) is a widely studied molecular target for the treatment of cancer and other diseases. We have approached the issue of modifying PKC function by targeting the C1 domain in the regulatory region of the enzyme. By using the X-ray c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17cab306f93ee2bc47d6850d862255c0
https://doi.org/10.1016/j.tet.2011.09.044
https://doi.org/10.1016/j.tet.2011.09.044
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 15:3717-3719
A convenient method for the synthesis of 1,5-disubstituted imidazoles has been developed on a polymeric support using base-promoted 1,3-dipolar cycloaddition reaction of p-toluenesulfonylmethyl isocyanide (TOSMIC) with immobilized imines under microw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47a091971e86d43de66d08f3f16d2cd8
https://doi.org/10.1016/j.bmcl.2005.05.066
https://doi.org/10.1016/j.bmcl.2005.05.066
Autor:
Jari Yli-Kauhaluoma, Tero Wennberg, Irene Kylänlahti, Kalevi Pihlaja, Pia Vuorela, Teemu H. Teeri, Tiina Auerma, Karel D. Klika, Satu Koskela, P.P. Söderholm, Vladimir V. Ovcharenko, Miia Ainasoja
Publikováno v:
Planta. 233(1)
A previously isolated cDNA molecule from Gerbera hybrida (Asteraceae) codes for a new chalcone synthase-like polyketide synthase, 2-pyrone synthase (2PS). 2PS is able to synthesise 4-hydroxy-6-methyl-2-pyrone (triacetolactone), a putative precursor f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::240dac1741d94896a37dd3c94d7809e9
https://pubmed.ncbi.nlm.nih.gov/20878179
https://pubmed.ncbi.nlm.nih.gov/20878179
Autor:
Eija Kalso, Irene Kylänlahti, Kaarin Viljakka, Vesa K. Kontinen, Kim Lemberg, Jari Yli-Kauhaluoma
Publikováno v:
Anesthesia and analgesia. 102(6)
We studied the effects of the commonly used mu-opioid receptor agonists morphine, oxycodone, methadone and the enantiomers of methadone in thermal and mechanical models of acute pain and in the spinal nerve ligation model of neuropathic pain in rats.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0bb91daafd5f823e9afb9181e19d449
https://pubmed.ncbi.nlm.nih.gov/16717324
https://pubmed.ncbi.nlm.nih.gov/16717324
Autor:
Jari Yli-Kauhaluoma, Kirsi Harju, John Nielsen, Timo S. Paananen, Irene Kylänlahti, Mika Polamo
Publikováno v:
Journal of combinatorial chemistry. 8(3)
Study was made of the 1,3-dipolar cycloaddition of polymer-bound alkynes to azomethine imines generated in situ from N-aminopyridine iodides. Aromatization of the cycloadducts gives polymer-bound pyrazolopyridines that can be released from the resin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae360c87fc2d80d83a20770a98a8fd6d
https://pubmed.ncbi.nlm.nih.gov/16677003
https://pubmed.ncbi.nlm.nih.gov/16677003
Autor:
Jian Hong Peng, Liisa Ahtee, Irene Kylänlahti, Jari Yli-Kauhaluoma, Ronald J. Lukas, Esa R. Korpi, Heli Nousiainen, Jukka S. Pakkanen, Raimo K. Tuominen, Tommi Möykkynen
Publikováno v:
Journal of neurochemistry. 94(5)
(-)-Methadone acts as an agonist at opioid receptors. Both (+)- and (-)-enantiomers of methadone have been suggested to be potent non-competitive antagonists of alpha3beta4 neuronal nicotinic acetylcholine receptors (nAChRs). In the present study, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8da2512250ed259d8cbca77a36917c26
https://pubmed.ncbi.nlm.nih.gov/16000156
https://pubmed.ncbi.nlm.nih.gov/16000156
Autor:
Irene Kylänlahti, Tsutomu Sugeta, Katsuto Otake, Yoshihiro Takebayashi, Jari Yli-Kauhaluoma, Antero Laitinen
Publikováno v:
Laitinen, A, Takebayashi, Y, Kylanlahti, I, Yli-Kauhaluoma, J, Sugeta, T & Otake, K 2004, ' Ene reaction of allylbenzene and N-methylmaleimide in subcritical water and ethanol ', Green Chemistry, vol. 6, no. 1, pp. 49-52 . https://doi.org/10.1039/b304959k
Ene reaction of allylbenzene and N-methylmaleimide was studied in water and ethanol solvents at subcritical temperatures (220–310 °C). Subcritical water was inappropriate for this reaction, because it rapidly hydrolyzed N-methylmaleimide. Subcriti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::831600edb1adc6c4bb2550f8f08e843f
https://cris.vtt.fi/en/publications/da5faf53-56b4-48b0-b4dd-da1fb3cbc60b
https://cris.vtt.fi/en/publications/da5faf53-56b4-48b0-b4dd-da1fb3cbc60b
Publikováno v:
Journal of combinatorial chemistry. 3(6)
The Vilsmeier formylation has been introduced for the solid-phase functionalization of five different 2-carboxyindoles. The aldehyde functionality has been utilized in the preparation of O-benzylhydroxyureas.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9d2a174e71f48c2d7c1f1717458bcd0
https://pubmed.ncbi.nlm.nih.gov/11703149
https://pubmed.ncbi.nlm.nih.gov/11703149
Autor:
Antero Laitinen, Yoshihiro Takebayashi, Irene Kylänlahti, Jari Yli-Kauhaluoma, Tsutomu Sugeta, Katsuto Otake
Publikováno v:
Green Chemistry; Jan2004, Vol. 6 Issue 1, p49-52, 4p
Autor:
Antero Laitinen, Yoshihiro Takebayashi, Irene Kylänlahti, Jari Yli-Kauhaluoma, Tsutomu Sugeta, Katsuto Otake
Publikováno v:
Scopus-Elsevier
University of Helsinki
University of Helsinki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ad96612e4a57037f7febab0aa192fb16
http://www.scopus.com/inward/record.url?eid=2-s2.0-1442351241&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-1442351241&partnerID=MN8TOARS