Results 161 to 170 of about 6,839 (201)
Some of the next articles are maybe not open access.
Role of ornithine decarboxylase antizyme inhibitor in vivo
Genes to Cells, 2008Ornithine decarboxylase (ODC) antizyme inhibitor (AZI) has been shown to regulate ODC activity in cell cultures. However, its biological functions in an organism remain unknown. An embryonic stem (ES) cell clone was established, in which the Azin1 gene was disrupted by the gene trap technique.
Hua, Tang +6 more
openaire +2 more sources
Ornithine decarboxylase inhibitors and fetal growth retardation in mice
Teratology, 1983AbstractPutrescine (PUT) and the putrescine analogues, 1,3‐diaminopropane (DAP) and 1,6‐diaminohexane (DAH), were administered to pregnant female mice during the time of maximal fetal ornithine decarboxylase (ODC) activity, days 10–14 of gestation.
C A, Manen, R D, Hood, J, Farina
openaire +2 more sources
Kinetics of α-difluoromethylornithine: An irreversible inhibitor of ornithine decarboxylase
Clinical Pharmacology and Therapeutics, 1981We gave alpha-difluoromethylornithine (DFMO), a selective, irreversible inhibitor of ornithine decarboxylase, to six health men in single intravenous doses of 5 and 10 mg/kg body weight and oral doses of 10 and 20 mg/kg. Plasma concentrations were monitored during the 24 hr after each dose.
K D, Haegele +4 more
openaire +2 more sources
Allicin, a Potent New Ornithine Decarboxylase Inhibitor in Neuroblastoma Cells
Journal of Natural Products, 2020The natural product allicin is a reactive sulfur species (RSS) from garlic (Allium sativum L.). Neuroblastoma (NB) is an early childhood cancer arising from the developing peripheral nervous system. Ornithine decarboxylase (ODC) is a rate-limiting enzyme in the biosynthesis of polyamines, which are oncometabolites that contribute to cell proliferation ...
Chad R. Schultz +3 more
openaire +2 more sources
Biochimica et Biophysica Acta (BBA) - General Subjects, 1977
When spermidine, putrescine or 1,3-diaminopropane was injected (12.5 mumol/100 g body weight) into rats 1 h before thyrotropin, ornithine decarboxylase activity was increased by 75--150% over control levels. However, when greater than or equal to 75 mumol polyamine/100 g body weight was injected, thyrotropin-activated activity was inhibited by 70--95%.
Y, Friedman +3 more
openaire +2 more sources
When spermidine, putrescine or 1,3-diaminopropane was injected (12.5 mumol/100 g body weight) into rats 1 h before thyrotropin, ornithine decarboxylase activity was increased by 75--150% over control levels. However, when greater than or equal to 75 mumol polyamine/100 g body weight was injected, thyrotropin-activated activity was inhibited by 70--95%.
Y, Friedman +3 more
openaire +2 more sources
Histochemical localization of ornithine decarboxylase with a labelled suicidal enzyme inhibitor
Biochemical and Biophysical Research Communications, 1980Abstract We describe a new technique for cytochemical localization of ornithine decarboxylase by the use of a synthesized conjugate of rhodamine bound to α-difluoromethylornithine a suicidal inhibitor of the enzyme. The labelled inhibitor retained its specificity and irreversibility towards ornithine decarboxylase inhibition.
G M, Gilad, V H, Gilad
openaire +2 more sources
Journal of Enzyme Inhibition, 1989
Two fluorescent derivatives have been made from alpha-difluoromethyl ornithine by linking the carboxyl group of the ornithine derivatives to fluorescent amines. alpha-difluoromethyl ornithine is a potent inhibitor of ornithine decarboxylase, an enzyme which plays an essential role in cell division.
F S, Steven +3 more
openaire +2 more sources
Two fluorescent derivatives have been made from alpha-difluoromethyl ornithine by linking the carboxyl group of the ornithine derivatives to fluorescent amines. alpha-difluoromethyl ornithine is a potent inhibitor of ornithine decarboxylase, an enzyme which plays an essential role in cell division.
F S, Steven +3 more
openaire +2 more sources
Life Sciences, 1983
The subcellular localisation of ornithine decarboxylase and of its synthetic irreversible inhibitor, alpha-difluoromethylornithine, was investigated in control rat livers and in livers of animals in which the enzyme was induced by partial hepatectomy or by treatment with dexamethasone.
openaire +2 more sources
The subcellular localisation of ornithine decarboxylase and of its synthetic irreversible inhibitor, alpha-difluoromethylornithine, was investigated in control rat livers and in livers of animals in which the enzyme was induced by partial hepatectomy or by treatment with dexamethasone.
openaire +2 more sources
[Aminooxypropylamine--an effective inhibitor of ornithine decarboxylase in vitro and in vivo].
Bioorganicheskaia khimiia, 1986Hydroxylamine-containing analogues of putrescine and cadaverine have been found effective in inhibiting the mouse liver ornithine decarboxylase, the best among synthesized were 1-aminooxy-3-aminopropane (I50 2.10(-8) M) and 1-aminooxy-4-aminobutane (I50 2.10(-7) M). The inhibitory effect of these substances on the mouse liver ornithine-transaminase and
R M, Khomutov +4 more
openaire +2 more sources
Chemischer Informationsdienst, 1974
Abstract5‐Chlor‐2‐pentanon (I) reagiert mit Phthalimidkalium (II) zum Imid (III), aus dem das Hydantoin (IV) erhalten wird.′Die Hydrolyse liefert die geschützten Methylomithin‐Derivate (V) und (VI), die zum Ornithin (VII) verseift werden.
M. M. ABDEL‐MONEM +2 more
openaire +1 more source
Abstract5‐Chlor‐2‐pentanon (I) reagiert mit Phthalimidkalium (II) zum Imid (III), aus dem das Hydantoin (IV) erhalten wird.′Die Hydrolyse liefert die geschützten Methylomithin‐Derivate (V) und (VI), die zum Ornithin (VII) verseift werden.
M. M. ABDEL‐MONEM +2 more
openaire +1 more source

