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Leukemia K562 cells

Ask A, Persson L, Rehnholm A, Frostesjo L, Holm I, Heby O (1993) Development of resistance to hydroxyurea during treatment of human myelogenous leukemia K562 cells with alpha-difluoromethylornithine as a result of coamplification of genes for ornithine decarboxylase and ribonucleotide reductase R2 subunit. Cancer Res 53 5262-5268... [Pg.61]

Cao P, Ding H, Ge HM et al. (2007) Synthesis and cytotoxic evaluation of substituted urea derivatives as inhibitors of human-leukemia K562 cells. Chem Biodivers 4 881-186... [Pg.13]

Oyama Y, Tonemori S. Cytotoxic activity of maytanprine isolated from M. diversifolia in human leukemia K562 cells. Biol. Pharm. [Pg.1195]

SIN-1 induced higher antiproliferation activity in BCR-ABL+ leukemia K562 cells when compared to normal hemopoietic cells [52]. NO-mediated apoptosis is shown to be inhibited in myeloid leukemia cells by the elevation of intracellular iron. [Pg.144]

Luxemburgia nobilis Eichl. (leaves) Ochnaflavone (I-3, 0,II-4 —flavone-flavanone)-. 11-2,3-Dihydroochnaflavone (225). Inhibitor of DNA topoisomerases. (225) was cytotoxic to murine Ehrlich carcinoma and human leukemia K562 cells. (225) inhibited the activity of human DNA topoisomerases I and Il-a. (225) is a DNA interacting agent, which causes DNA unwinding in an assay with topoisomerase I. Likhitwitayawuid e al., 2001 [290] D Oliveira et al 2002[291],2005[59]. [Pg.127]

SWCNT composite was found to be homogenous, hydrophilic, conductive, and biocompatible and was further utilized for immobilization of leukemia K562 cells on a gold electrode to form an impedance ceU sensor with a relatively low detection limit. By using ILs as intermediary solvents, the fabricated composite from cellulose and CNTs effectively combines the biocompatibUity of the former and the conductivity of the latter. It is believed that these methods would have great potential from the creation of novel biocomposites to the use as scaffolds, biosensors, drug carriers, and biological transporters. [Pg.406]

Li B-Z, Zhuang W-Z, Oien P, Fu J-X (2008) Effects of RNA interference targeting hypoxia-inducible factor-la (HIF-la) on chemosensitivity of leukemia K562 cells towards homoharringtonine. Qiin J Cancer 27(7) 47-52... [Pg.1465]

Figure 10.9 (a) Scheme of thei-Motif telomeric DNA-based electrochemical DNA (E-DNA) sensor, (b) E-DNA sensor that detects intracellular SWNTs In extracts of the human chronic myelogenous leukemia K562 cells. (Inset) Calibration curve measured in 1 x KT cell mb cell supernatant (cells were cultured In the absence of SWNTs). Reproduced with permission from [76]. Copyright 2009, American Chemical Society... [Pg.310]

Wang, C. L.,Ng, T. B., Yuan, F., Liu, Z. K., Liu,F. Induction of apoptosis in human leukemia K562 cells by cyclic lipo peptide from Bacillus subtilis natto T-2. Peptides 2007, 28, 1344-1350. [Pg.109]

Aoki, S., Kong, D., Matsui, K, Rachmat, R., and Kobayashi, M. (2004b) Sesquiterpene anfhraquinones, from a marine sponge, induce erythroid differentiation in human chronic myelogenous leukemia, K562 cells. Chem. Pharm. Butt., 52, 935-937. [Pg.1207]

Some of the acetoxylated derivatives are cytotoxic to leukemia K562 cells, with IC50 values varying from 0.7 to 24 [xM (Morris et al., 1998b). [Pg.1800]

Sakurada K, Zheng B, Kuo JF (1992) Comparative effects of protein phosphatase inhibitors (okadaic acid and calyculin A) on human leukemia HL60, HL60/ADR and K562 cells. Biochem Biophys Res Commun 187 488-492... [Pg.88]

Ikegawa T, Ushigome F, Koyabu N, et al. Inhibition of P-glycoprotein by orange juice components, polymethoxyflavones in adriamycin-resistant human myelogenous leukemia (K562/ADM) cells. Cancer Lett 2000 160(l) 21-28. [Pg.181]

The antiproliferative activity of 1,2,3-dithiazoles 168-176 has been tested in vitro on human myeloid leukemia K562 and L1210 murine leukemia cell lines and compared to the antiproliferative effects of the natural product distamycin A. All the imines 168-176 are active at concentration ranging from 3 to 10 pM and they retain antiproliferative activities comparable to those exhibited by distamycin A. [Pg.32]

M. Nakamura, K. Kirito, J. Yamanoi, T. Wainai, H. Nojiri, and M. Saito, Gang-lioside GM3 can induce megakaryocytoid differentiation of human leukemia cell line K562 cells, Cancer Res., 51 (1991) 1940-1945. [Pg.470]

The cytotoxicities of these compounds (Figure 8) were examined in leukemia cell line K562 cells and colon cancer cell line SW620 cells with MTS... [Pg.28]

Amagasaki, T., Green, R., Jacobsen, D. W. 1990. Expression of transcobalamin II receptors by human leukemia K562 and HL-60 cells. Blood, 76, 1380-6. [Pg.252]

Vegetable TSPS Camelia sinensis (tea) K562 cells (human myelogenous leukemia) in-vivo [40]... [Pg.5]

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See also in sourсe #XX -- [ Pg.76 ]

See also in sourсe #XX -- [ Pg.285 ]



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