Zobrazeno 1 - 10
of 154
pro vyhledávání: '"D.-E. SOK"'
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb3723d599f2cf1c4b419824c813882a
https://doi.org/10.1002/chin.199817101
https://doi.org/10.1002/chin.199817101
Autor:
Mee Ree Kim, D E Sok
Publikováno v:
Biochemical Journal. 286:435-440
p-Nitrophenylphosphocholine phosphodiesterase activity was purified 5000-fold from mouse brain by treatment of membranes with Bacillus cereus phospholipase C preparation and sequential chromatographies on concanavalin A-Sepharose and CM-Sephadex colu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd935aea69167642b889961d7a31cf06
https://doi.org/10.1042/bj2860435
https://doi.org/10.1042/bj2860435
Publikováno v:
Phytomedicine : international journal of phytotherapy and phytopharmacology. 14(10)
Neuroprotective effect of honokiol (HK), orally administered, on oxidative damage in the brain of mice challenged with N-methyl-d-aspartic acid (NMDA) was examined. HK (1-100 mg/kg) was administered to Institute of Cancer Research (ICR) male mice thr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::076eeaea28e3af6e41bc1fdba47e1fd3
https://pubmed.ncbi.nlm.nih.gov/17470388
https://pubmed.ncbi.nlm.nih.gov/17470388
Autor:
Mee Ree Kim, D E Sok
Publikováno v:
Biochemical Journal. 284:641-643
A Zn(2+)-glycerophosphocholine cholinephosphodiesterase (EC 3.1.4.38) purified from mouse brain was found to be reversibly inhibited by tellurium tetrachloride. This effect was characterized by a competitive pattern of inhibition, with apparent Ki va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f0e8286884d8c467179cb6abce6fb0d
https://doi.org/10.1042/bj2840641
https://doi.org/10.1042/bj2840641
Publikováno v:
Neurochemical research. 25(11)
5'-Nucleotidase, responsible for the conversion of adenosine-5'-monophosphate into adenosine, was purified from bovine brain membranes, and subjected to oxidative inactivation. The 5'-nucleotidase activity decreased slightly after the exposure to eit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c9e6877e7406d27be8078eb9488d7e93
https://pubmed.ncbi.nlm.nih.gov/11071366
https://pubmed.ncbi.nlm.nih.gov/11071366
Publikováno v:
Archiv der Pharmazie. 333(4)
2- or 6-(1-Hydroxyiminoalkyl)-5,8-dimethoxy-1,4-naphthoquin-one (DMNQ) and 6-(1-propyloxyimino- alkyl)-DMNQ derivatives were synthesized, and their inhibitory effects on DNA topoisomerase-I (TOPO-I) and antiproliferative activities against L1210 cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1ba4f90eb2977aca04e4c715ccf3d7a0
https://pubmed.ncbi.nlm.nih.gov/10816900
https://pubmed.ncbi.nlm.nih.gov/10816900
Publikováno v:
Neurochemical research. 24(12)
Brain glycosylphosphatidylinositol-specific phospholipase D (GPI-PLD)-catalyzed conversion of amphiphilic form of Zn2+ -glycerophosphocholine cholinephosphodiesterase (Amp-GPC PDE) into hydrophilic form was investigated in the presence of natural amp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c94955a9078dfcbccfb1ba684f9e8ce5
https://pubmed.ncbi.nlm.nih.gov/10591409
https://pubmed.ncbi.nlm.nih.gov/10591409
Publikováno v:
Neurochemical research. 24(8)
Enzymatic release of Zn(2+)-glycerophosphocholine (GPC)cholinephosphodiesterase, as an amphiphilic form, from bovine brain membranes was examined. Of various membrane hydrolases, bee PLA2 was the most effective in the release of the GPC cholinephosph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::949bc90aec3ce9f0e15dd70c986e9003
https://pubmed.ncbi.nlm.nih.gov/10478944
https://pubmed.ncbi.nlm.nih.gov/10478944
Publikováno v:
Bioorganicmedicinal chemistry letters. 9(16)
6-(1-Hydroxyalkyl)-5,8-dimethoxy-1,4-naphthoquinones, expressing a higher reactivity in conjugation with glutathione, showed a greater potency in the inhibition of DNA topoisomerase-I and the cytotoxicity against L1210 cells than 2-(1-hydroxyalkyl)-D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7283936b21e3615610f8f11eac0e1951
https://pubmed.ncbi.nlm.nih.gov/10476878
https://pubmed.ncbi.nlm.nih.gov/10476878
Publikováno v:
Archiv der Pharmazie. 331(12)
A series of 2-alkylated anthracene-1,4,9,10-tetraone (ATO) derivatives were synthesized, and their antitumor action in ICR mice bearing S-180 cells and antiproliferative activity against L1210 cells were evaluated. Overall, the introduction of an alk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6c38edef9a8273ddcefaf0bcac6e9c3f
https://pubmed.ncbi.nlm.nih.gov/9923192
https://pubmed.ncbi.nlm.nih.gov/9923192