Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Bela Ternai"'
Autor:
Gideon M. Polya, Bela Ternai, Mery Hasmeda, Wilawan Mahabusarakam, Zhe Xiong Lu, Prapaipit Chamsuksai Ternai
Publikováno v:
Chemico-Biological Interactions. 114:121-140
A series of prenylated xanthones are variously potent inhibitors of the catalytic subunit (cAK) of rat liver cyclic AMP-dependent protein kinase (PKA), rat brain Ca2+ and phospholipid-dependent protein kinase C (PKC), chicken gizzard myosin light cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f7e6de6c8c18ac2b1682c034532f9ac
https://doi.org/10.1016/s0009-2797(98)00049-0
https://doi.org/10.1016/s0009-2797(98)00049-0
Publikováno v:
Biological Chemistry Hoppe-Seyler. 375:527-536
The phenanthrenemethanol antimalarial halofantrine is a potent inhibitor of bovine heart and rat liver cyclic AMP-dependent protein kinase catalytic subunit (cAK) (IC50 values 2.1 microM and 0.6 microM, respectively). The inhibition of rat liver cAK
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1824526e4d5a9a4fd6b09ff8c46bfa68
https://doi.org/10.1515/bchm3.1994.375.8.527
https://doi.org/10.1515/bchm3.1994.375.8.527
Publikováno v:
Planta Medica. 59:525-528
Methanolic extracts of leaves, flowers, stems, bark, and other parts of representative plants of the Myrtaceae, specifically of the EUCALYPTUS, MELALEUCA, THRYPTOMENA, CALLISTOMEN, ACMENA, AND ANGOPHORA genera, variously contain high levels of inhibi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86700517e1a60d96a3d56f0683e987a9
https://doi.org/10.1055/s-2006-959753
https://doi.org/10.1055/s-2006-959753
Publikováno v:
Biological Chemistry Hoppe-Seyler. 373:205-212
Rat liver cyclic AMP-dependent protein kinase catalytic subunit (cAK), assayed using the synthetic peptide substrate, LRRASLG, is inhibited by a range of plant-derived flavonoids. In general, maximal inhibitory effectiveness (IC50 values 1 to 2 micro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b297a37719162011e0f30423e0d6f8c0
https://doi.org/10.1515/bchm3.1992.373.1.205
https://doi.org/10.1515/bchm3.1992.373.1.205
Publikováno v:
Plant Science. 78:165-175
Wheat embryo Ca2+-dependent protein kinase (CDPK) is inhibited by a variety of long chain amphiphilic compounds that also inhibit avian myosin light chain kinase (MLCK), namely by straight chain alkylamines, alkyltrimethylammonium halides and N- alky
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da29e4c8a4d3c2c1cb58457527ed2dfc
https://doi.org/10.1016/0168-9452(91)90195-e
https://doi.org/10.1016/0168-9452(91)90195-e
Publikováno v:
Phytochemistry. 44(5)
The prenylated isoflavone warangalone from the insecticidal plant Derris scandens is a selective and potent inhibitor of rat liver cyclic AMP-dependent protein kinase catalytic subunit (cAK) (IC50 3.5 microM). The inhibition of rat liver cAK by waran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::849140bf73c820bf3011b11b264cbf2d
https://pubmed.ncbi.nlm.nih.gov/9115691
https://pubmed.ncbi.nlm.nih.gov/9115691
Publikováno v:
Biological chemistry Hoppe-Seyler. 373(9)
A variety of anthraquinone (anthracene-9,10-dione) derivatives inhibits rat brain Ca(2+)- and phospholipid-activated protein kinase C (PKC) of which the most potent inhibitors are mitoxantrone (1,4-dihydroxy-5,8-bis[2-(hydroxyethylamino)-ethylamino]-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dee26eb81e046f39bbbebc6f5e3dde7
https://pubmed.ncbi.nlm.nih.gov/1466788
https://pubmed.ncbi.nlm.nih.gov/1466788
Publikováno v:
Biological chemistry Hoppe-Seyler. 372(9)
Avian myosin light chain kinase (MLCK) is inhibited by a range of plant-derived flavonoids. Maximal inhibition requires 2,3-unsaturation and polyhydroxylation of two of the three flavonoid rings. Phosphorylation of a synthetic myosin light chain-rela
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::325244bc8af5b4ed80a5c70c8e90c5a7
https://pubmed.ncbi.nlm.nih.gov/1772594
https://pubmed.ncbi.nlm.nih.gov/1772594
Publikováno v:
Medical Journal of Australia. 152:54-54
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a29d7705a972daa210e3aa0c388d776b
https://doi.org/10.5694/j.1326-5377.1990.tb124447.x
https://doi.org/10.5694/j.1326-5377.1990.tb124447.x
Autor:
Luisa Cook, Bela Ternai
Publikováno v:
Biological Chemistry Hoppe-Seyler. 370:11-20
Inhibition of human leucocyte elastase by oleic acid and the structurally related 3-(1'-oxo-7'-carboxyheptyl)-4-hydroxy-6-octyl-2-pyrone is considerably enhanced by the addition of Cu2+, Zn2+ and, to a lesser extent, Co2+ and Ca2+. Sulindac sulfide a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd90bb91e1443f865d0d8621d461db5a
https://doi.org/10.1515/bchm3.1989.370.1.11
https://doi.org/10.1515/bchm3.1989.370.1.11