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Anti-leukemic

Zee-Cheng KY, Cheng CC. Common receptor-complement feature among some anti-leukemic compounds. J Pharm Sci 1970 59 1630-4. [Pg.206]

The histone deacetylase inhibitor ITF2357 has anti-leukemic activity in vitro and in vivo and inhibits IL-6 and VEGF production by stromal cells. Leukemia,... [Pg.219]

Loss of the p53 tumor suppressor gene has been shown to impede the anti-leukemic response to BCR-ABLl inhibition (43). Another mechanism for resistance that is independent of BCR-ABLl and that has been demonstrated in vitro is over-expression of SRC-related kinases such as LYN (44). It appears that kinases from the SRC family mediate signaling of BCR-ABLL This has been demonstrated in vitro with the use of SRC kinase inhibitors and SRC mutants that are kinase defective (45,46,47). [Pg.137]

Gonzalez IC, Forsyth CJ (2000) Total Synthesis of Thyrsiferyl 23-Acetate, a Specific Inhibitor of Protein Phosphatase 2A and an Anti-Leukemic Inducer of Apoptosis. J Am Chem Soc 122 9099... [Pg.411]

Extracts of Amaryllidaceae alkaloids have long been used in traditional medicine for the treatment of a variety of illnesses. As early as the fourth century B.C., Hippocrates had reputedly advised the use of preparations of Amaryllidaceae plants to control uterine tumours [157]. More recently, a systematic bioassay of these alkaloids of different structural types has revealed a diversity of interesting biological properties. Thus, (+)-pretazettine (369) [158,159], and ungeremine (182) [160] show anti-leukemic activity. Cytotoxicity was observed for (-)-lycorine (245) [161], (-)-pseudolycorine (574) [162], 6-a-hydroxycrinamine (575) [163],... [Pg.558]

Furlong MT et al (2012) A validated LC-MS/MS assay for the simultaneous determination of the anti-leukemic agent dasatinib and two pharmacologically active metabolites in human plasma application to a clinical pharmacokinetic study. J Pharm Biomed Anal 58 ... [Pg.244]

The carbene-insertion pathway has recently been applied in total asymmetric syntheses of the anti-leukemic alkaloid, (—)-agelastatin A, and the dibromo analog, (-)-agelastatin B (02JA9060, 02JOC7096). Treatment of the (oxazolidinonyl)propynyliodonium triflate 250 with sodium />-toluenesulfinate leads to a mixture of the bicyclic oxazolidinone 251 and the carbenic rearrangement product 252 (Scheme 70) compound 251 is a key intermediate in the agelastatin synthesis. [Pg.268]

Shadidi, M. and M. Sioud (2001). An anti-leukemic single chain Fv antibody selected from a synthetic human phage antibody library. Biochem Biophys Res Commun 280(2) 548-552. [Pg.125]

G. Klopman and O. T. Macina, Mol. Pharmacol., 31, 457 (1987). Computer-Automated Structure Evaluation of Anti-leukemic 9-Anilinoacridines. [Pg.214]

Jones RJ, Sharkis SJ, Miller CB, Rowin-sky EK, Burke PJ, May WS. 1990. Bryostatin 1, a unique biologic response modifier anti-leukemic activity in vitro. Blood 75 1319-23... [Pg.227]

PP2A impaired activity is a common event in acute myeloid leukemia and its activation by forskolin has a potent anti-leukemic effect. Leukemia 25 606-614... [Pg.302]

Usnic acid (7.53)—a highly biologically active dibenzofuran—is a phenol oxidation product of an acylphlorogludnol. It is produced by numerous lichens, including several Usnea species. Apart from its antibiotic and anti-leukemic activity, it has insect anti-feedant activity. Its presence may account for the observation that many lichens are resistant to serious insect attack. [Pg.141]

Myers, D., Yanishevski, Y., Masson, E., Irvin, J., Evans, W., and Uckun, F. (1995) Favorable pharmacodynamic features and superior anti-leukemic activity of B43 (anti-CD19) immunotoxins containing two pokeweed antiviral protein molecules covalently linked to each monoclonal antibody molecule. Leuk. Lymphoma 18, 93-102. [Pg.36]

NR Ferringi, JL McLaughlin, RG Powel, CR Smith. Use of potato disk and brine shrimp bioassay to detect activity and isolate piceatanol as the anti-leukemic principle from the seeds of Euphobia lagascae. J Nat Prod Al 347-352, 1984. [Pg.621]

Table 8. Anti leukemic Activity of Bisbrusatolyl and Brusatolyl Esters and Related Compounds against P>388 Lymphocytic Leukemia Cell Growth in BDFl Mice... Table 8. Anti leukemic Activity of Bisbrusatolyl and Brusatolyl Esters and Related Compounds against P>388 Lymphocytic Leukemia Cell Growth in BDFl Mice...
See, for example, Andrivon, W., et ai. A new anthracycline with potent anti-leukemic activity overcomes P-glycoprotein multidrug resistance. Leuk. Res. 1998, 22, 719-725. [Pg.428]

Find the full chemical name, the drug name, and chemical structure of the anti-leukemic developed by Hitchings and Elion. [Pg.431]

Kupchan, S. M., a. L. Desserttne, B. T. Blaylock, and R. F. Bryan, Isolation and stmcture elucidation of allamandin, an anti-leukemic iridoid lactone from Allamanda cathartica, J. Org. Chem., 39, 2477-2482 (1974). [Pg.365]

Approximately 30% of patients with AML exhibit dys-regulation of the FLT3 oncogene, due either to mutation or amplification of internal tandem repeats (ITD) (Lee et al. 2005). Such abnormalities carry a relatively poor prognosis. This has prompted the development of FLT3 inhibitors for such patients (e.g., PKC-412), either as monotherapy, or more commonly, in combination with standard anti-leukemic regimens (Weisberg et al. 2002 Stone et al. 2005 Furukawa et al. 2007). [Pg.197]

Dirsch, V.M., Antlsperger, D.S., Hentze, H., and Vollmar, A.M. 2002. Ajoene, an experimental anti-leukemic drug mechanism of (tell death. Leukemia 7(5(1) 74—83. [Pg.450]

Chakrapani, H., Goodblatt, M.M., Udupi, V., Malaviya, S., Shami, P.J., Keefer, L.K., and Saavedra, J.E. (2008). Synthesis and in vitro anti-leukemic activity of structural analogues of js-k, an anti-cancer lead compound. Bioorg. Med. Chem. Lett. 18, 950-953. [Pg.124]


See other pages where Anti-leukemic is mentioned: [Pg.144]    [Pg.61]    [Pg.154]    [Pg.4694]    [Pg.661]    [Pg.188]    [Pg.903]    [Pg.217]    [Pg.4693]    [Pg.147]    [Pg.180]    [Pg.73]    [Pg.51]    [Pg.102]    [Pg.194]    [Pg.358]    [Pg.175]    [Pg.62]    [Pg.60]   
See also in sourсe #XX -- [ Pg.175 ]




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