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Lymphocytic leukemia

Griseofulvia [126-07-8] (54) coataias the pblorogluciaol aucleus. It is an important oral antifungal agent ia humans and animals, elaborated by certain strains of Penicillium. One synthesis of griseofulvia is based oa the appropriately substituted pblorogluciaol (196). Uvaretia [58449-06-2] (55), which is extracted from JJvaria acuminata inhibits lymphocytic leukemia (200). [Pg.386]

Biological Activity. The maytansinoids possess antitumor activity, particulady against P 388 lymphocytic leukemia, B 16 melanocarcinoma, and Lewis lung carcinoma. A number of semisynthetic esters of maytansinol have been prepared and exhibit good antileukemic activity (52,255). The maytansides lack antitumor activity, indicating that the ester at C-3 is a requirement for activity (50,52). The carbinolamide also appears to be necessary for... [Pg.505]

USP (Oncovin) vindesine sulfate [59917-39 ] C43H55N5O7 -H2S0 852.01 (50) chil-dren lymphocytic leukemia Hodgkin s disease non-Hodg-kin s lymphomas Wilm s tumor neuroblastoma rhabdomyosarcoma, investigational dmg (paresthesias, foot drop, double vision, etc) constipation ileus alopecia leu-kopenia (occasional) ... [Pg.441]

Leptosins D-F (258a-c, Scheme 39) [94JCS(P1)1859] were isolated by Takahashi and co-workers from the culture of a strain of Leptosphaeria sp. as cytotoxic substances against the P388 lymphocytic leukemia cell line comparable to that of mitomycin C. Utilizing the nucleophilic substitution reaction of 1-hydroxytryptamines, a simple methodology for the synthesis of core structures of leptosins has been developed (2000H1255). [Pg.139]

O Brien S, Moore JO, Boyd TE et al (2007) Randomized phase III trial of fludarabine plus cyclophosphamide with or without oblimersen sodium (Bcl-2 antisense) in patients with relapsed or refractory chronic lymphocytic leukemia. J Clin Oncol 25(9) 1114-1120... [Pg.188]

This is a humanized anti-CD52 monoclonal antibody. At present it is in clinical use after bone marrow transplantation and for the treatment of refractory chronic lymphocytic leukemia. [Pg.619]

A copper(II) complexes of 5-phenylazo-3-methoxy salicylidene thiosemicarbazone has been shown to have promising growth inhibition activity against P388 lymphocytic leukemia cells sensitive and resistant to adriamycin [196], The complex involves ON coordination of two deprotonated ligands and v(CS) is reported to be unaltered in intensity and position in the complex from its position in the spectrum of the ligand. Inhibition studies with the uncomplexed thiosemicarbazone indicating an important role for the copper(II). [Pg.30]

The electronic spectra and magnetic susceptibility of [Ni(21)Cl2] were found to be consistent with a five-coordinate high spin complex. This complex has greater antitumor activity against P388 lymphocytic leukemia test system in mice than cobalt(II), copper(II), zinc(II) and platinum(II) complexes of 21 [187],... [Pg.41]

Although 4-methyl-5-amino-1-formylisoquinoline thiosemicarbazone, 22, also forms [Ni(22)Cl2] with chemical properties similar to [Ni(21)Cl2], it, along with other metal complexes of 22, showed no activity against P388 lymphocytic leukemia test system in mice [202]. [Pg.41]

A series of paramagnetic [NiL-2H] complexes have been isolated in which L = 2,6-diacetylpyridine bis(azacyclothiosemicarbazones) with Ni(II) assuming a distorted five-coordinate structure with d-d bands at about 7250, 10510, 12500, 14400, 19200 and 20500 cm [153], None of these Ni(II) complexes were reported to have activity against the P388 lymphocytic leukemia test system in mice. [Pg.41]

Mercaptopurine (6-MP) is an oral purine analog that is converted to a ribonucleotide to inhibit purine synthesis. Mercaptopurine is converted into thiopurine nucleotides, which are catabolized by thiopurine S-methyltransferase (TPMT), which is subject to genetic polymorphisms and may cause severe myelosuppression. TPMT status may be assessed prior to therapy to reduce drug-induced morbidity and the costs of hospitalizations for neutropenic events. Mercaptopurine is poorly absorbed, with a time to peak concentration of 1 to 2 hours after an oral dose. The half-life is 21 minutes in pediatric patients and 47 minutes in adults. Mercaptopurine is used in the treatment of acute lymphocytic leukemia and chronic myelogenous leukemia. Significant side effects include myelosuppression, mild nausea, skin rash, and cholestasis. When allopurinol is used in combination with 6-MP, the dose of 6-MP must be reduced by 66% to 75% of the usual dose because allopurinol blocks the metabolism of 6-MP. [Pg.1285]

Teniposide, a topoisomerase II inhibitor, is administered as an infusion over 30 to 60 minutes to prevent hypotension. The pharmacokinetics are described by a three-compartment model, with an a half-life of 0.75 hours, a (5 half-life of 4 hours, and a terminal half-life of 20 hours. Considerable variability in clearance of teniposide in children has been reported.17 Teniposide has shown activity in the treatment of acute lymphocytic leukemia, neuroblastoma, and non-Hodgkin s lymphoma. Side effects include myelosuppression, nausea, vomiting, mucositis, and venous irritation. Hypersensitivity reactions may be life-threatening. [Pg.1288]

Alemtuzumab is the antibody to the CD52 receptor present on B and T lymphocytes. The pharmacokinetics of alemtuzumab demonstrate a terminal half-life of 7 days. Alemtuzumab has shown clinical activity in the treatment of chronic lymphocytic leukemia. Severe and prolonged (6 months) immunosuppression may result, which necessitates prophylaxis with cotrimox-azole and antivirals to prevent opportunistic infections. [Pg.1294]

Precursor B-cell neoplasm Precursor B-lymphoblastic leukemia/lymphoma Mature (peripheral) B-cell neoplasms B-cell chronic lymphocytic leukemia/small lymphocytic lymphoma... [Pg.1374]

Compare the classification systems for acute lymphocytic leukemia (ALL) and acute nonlymphocytic leukemia (ANLL). [Pg.1397]


See other pages where Lymphocytic leukemia is mentioned: [Pg.489]    [Pg.434]    [Pg.437]    [Pg.443]    [Pg.309]    [Pg.327]    [Pg.72]    [Pg.140]    [Pg.60]    [Pg.87]    [Pg.129]    [Pg.54]    [Pg.150]    [Pg.1261]    [Pg.576]    [Pg.584]    [Pg.585]    [Pg.585]    [Pg.590]    [Pg.591]    [Pg.647]    [Pg.78]    [Pg.609]    [Pg.88]    [Pg.104]    [Pg.41]    [Pg.1286]    [Pg.1286]    [Pg.1286]    [Pg.1287]    [Pg.1289]    [Pg.1290]    [Pg.1292]    [Pg.1293]    [Pg.1295]    [Pg.1374]   
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See also in sourсe #XX -- [ Pg.158 ]

See also in sourсe #XX -- [ Pg.925 ]

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Acute lymphocytic leukemia

Acute lymphocytic leukemia case study

Acute lymphocytic leukemia chemotherapy

Acute lymphocytic leukemia classification

Acute lymphocytic leukemia incidence

Acute lymphocytic leukemia infection

Acute lymphocytic leukemia maintenance therapy

Acute lymphocytic leukemia relapsed

Acute lymphocytic leukemia remission induction

Acute lymphocytic leukemia treatment

B-cell chronic lymphocytic leukemia

Baccharis gaudichaudiana in P-388 lymphocytic leukemia

Brain Tumors and Acute Lymphocytic Leukemia

Chronic lymphocytic leukemia

Chronic lymphocytic leukemia Alemtuzumab

Chronic lymphocytic leukemia Rituximab

Chronic lymphocytic leukemia case study

Chronic lymphocytic leukemia chemotherapy

Chronic lymphocytic leukemia clinical presentation

Chronic lymphocytic leukemia diagnosis

Chronic lymphocytic leukemia evaluation

Chronic lymphocytic leukemia monoclonal antibodies

Chronic lymphocytic leukemia prognosis

Chronic lymphocytic leukemia staging

Chronic lymphocytic leukemia treatment

Chronic lymphocytic leukemia/small

Common acute lymphocyte leukemia

Duocarmycin in lymphocyte leukemia

Leukemia, P388 mouse lymphocytic

Lymphocyte leukemia

Lymphocyte leukemia

Lymphocytic leukemia system

Lymphomas chronic lymphocytic leukemia/small

Mouse lymphocytic leukemia

Murine lymphocytic leukemia

Non-lymphocytic leukemia

P-388 (murine lymphocytic leukemia

P-388 lymphocytic leukemia

P-388 lymphocytic leukemia cell

Small lymphocytic leukemia

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