Zobrazeno 1 - 10
of 114
pro vyhledávání: '"I B Linden"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Psychopharmacology. 156:402-409
Rationale:L-Dopa induces dyskinesias during the treatment of Parkinson's disease and also in primates with nigrostriatal lesions produced by MPTP, but it is claimed that L-dopa does not provoke dyskinesia in humans or monkeys with an intact or mildly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c76c25bf00f4d1dcc0b579b3a60df9b9
https://doi.org/10.1007/s002130100733
https://doi.org/10.1007/s002130100733
Publikováno v:
Acta Neurologica Scandinavica. 65:188-189
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b2aa9710d3e79900ae7c6a14ee5bf64
https://doi.org/10.1111/j.1600-0404.1982.tb03445.x
https://doi.org/10.1111/j.1600-0404.1982.tb03445.x
Autor:
H, Haikala, I B, Linden
Publikováno v:
Journal of cardiovascular pharmacology. 26
This review compares the mechanisms of action of the calcium-sensitizing agents levosimendan, pimobendan, MCI-154, and EMD 53998. By using purified human recombinant troponin-C (cTnC), the role of cTnC as a target protein for these compounds was inve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ef7e0107081ec3ec4127856f0c90d2b
https://pubmed.ncbi.nlm.nih.gov/8907127
https://pubmed.ncbi.nlm.nih.gov/8907127
Autor:
P. A. Aho, I.-B. Linden
Publikováno v:
Scandinavian journal of gastroenterology. 27(2)
Nitecapone (3-100 mg/kg orally) dose-dependently (40-97%) decreased the macroscopic gastric lesions induced by ethanol, NaOH, or HCl in the rat. The duration of protection was long, being still 70% at 6 h after dosing. Nitecapone (10-100 mg/kg orally
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29d21511c0dec9bd6c8694529af2f94d
https://pubmed.ncbi.nlm.nih.gov/1561527
https://pubmed.ncbi.nlm.nih.gov/1561527
Publikováno v:
Journal of Pharmaceutical Sciences. 73:106-108
□ A series of 2-acylaminoethanesulfonamides were synthesized by treating the corresponding sulfonyl chlorides with ammonia, a primary, or a secondary amine. A few compounds displayed marked anticonvulsant activity in mice when tested for their pote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf5d3c75fe9bced95ddad8a1520b5d08
https://doi.org/10.1002/jps.2600730128
https://doi.org/10.1002/jps.2600730128
Autor:
Sudrik, Vilas1 (AUTHOR), Bodkhe, Arjun2 (AUTHOR), Lawande, Shamrao1 (AUTHOR), Suryawanshi, Manohar1 (AUTHOR)
Publikováno v:
Polycyclic Aromatic Compounds. 2023, Vol. 43 Issue 3, p2071-2079. 9p.
Autor:
R, Bäckström, E, Honkanen, A, Pippuri, P, Kairisalo, J, Pystynen, K, Heinola, E, Nissinen, I B, Linden, P T, Männistö, S, Kaakkola
Publikováno v:
Journal of medicinal chemistry. 32(4)
A series of disubstituted catechol derivatives was synthesized and tested as potential COMT inhibitors. The most active compounds were more than 1000 times more potent (IC50 = 3-6 nM) in vitro than the known COMT inhibitor, 3',4'-dihydroxy-2-methylpr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e201e8ee3e95eb7c1861edcb46cd63fb
https://pubmed.ncbi.nlm.nih.gov/2704029
https://pubmed.ncbi.nlm.nih.gov/2704029
Publikováno v:
Acta dermato-venereologica. 59(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a025f8030b285b3d696f60505cb2f569
https://pubmed.ncbi.nlm.nih.gov/93372
https://pubmed.ncbi.nlm.nih.gov/93372
Publikováno v:
Neurochemistry international. 5(3)
A number of 2-phthalimidoethanesulphonamides, new derivatives of the inhibitory neuromodulator taurine, were tested for their anticonvulsant activity in maximal electroshock seizure and pentetrazole seizure threshold tests in mice. Certain lower N-al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ae5e759377b4af6ae0bfc982003a0b6
https://pubmed.ncbi.nlm.nih.gov/20487955
https://pubmed.ncbi.nlm.nih.gov/20487955