Results 241 to 250 of about 855,762 (278)
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Canadian Journal of Biochemistry, 1976
A group of substituted 5,8-quinolinequinones which exhibit antineoplastic activity and which are structurally related to the antitumor antibiotic streptonigrin induce single strand cleavage of PM2 covalently-closed circular-DNA (ccc-DNA) when reductively
J. Lown, S. Sim
semanticscholar +1 more source
A group of substituted 5,8-quinolinequinones which exhibit antineoplastic activity and which are structurally related to the antitumor antibiotic streptonigrin induce single strand cleavage of PM2 covalently-closed circular-DNA (ccc-DNA) when reductively
J. Lown, S. Sim
semanticscholar +1 more source
The Toxicologic Evaluation of Marcellomycin—An Antineoplastic Anthracycline Antibiotic
Drug and Chemical Toxicology, 1983Dose-related toxicologic effects of marcellomycin, an antineoplastic anthracycline antibiotic, were observed in single-dose studies in mice iv (43.05-67.65 mg/m2) and dogs iv (41.0-90.2 mg/m2), and in multiple-dose studies in dogs iv (9.8-29.6 mg/m2 2X/week for 6 weeks) and rats sc (9 weekly doses at 26.2-72.2 mg/m2).
R A, Buroker+5 more
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Chronic toxicity of adriamycin: A new antineoplastic antibiotic
Toxicology and Applied Pharmacology, 1972Abstract Adriamycin, a new antitumor antibiotic, was administered for 3 mo to rabbits and dogs by iv injection of daily single doses of 0.125, 0.250 and 0.5 mg/kg body weight. The lowest dose caused neither mortality nor any sign of toxicity with reference to body weight, blood picture and function and morphology of the liver, kidneys, heart and skin
Tea Chieli+4 more
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The Toxicological Evaluation of Carminomycin - An Antineoplastic Anthracycline Antibiotic
Drug and Chemical Toxicology, 1981Carminomycin, an anthracycline antibiotic discovered in the Soviet Union, possesses antitumor activity and is chemically related to adriamycin and daunorubicin. The toxic effects of carminomycin observed in single-dose toxicologic studies in mice iv (4.5-13.5 mg2) and po (18.9-52.2 mg/m2), rats iv (6.0-21.0 mg/m2), dogs iv (1.0-16.0 mg/m2) and po (16.0-
R A, Buroker, D F, Johnson, H, Madissoo
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International Journal of Oncology, 1994
The antibacterial and interactive effects of doxorubicin, cisplatin, cytarabine, vincristine, carmustine, mitoxantrone, methotrexate, bleomycin, 5-fluorouracil, epirubicin, DTIC, mitomycin, etoposide and estramustine phosphate on the antibacterial ...
P. Bergstrom+3 more
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The antibacterial and interactive effects of doxorubicin, cisplatin, cytarabine, vincristine, carmustine, mitoxantrone, methotrexate, bleomycin, 5-fluorouracil, epirubicin, DTIC, mitomycin, etoposide and estramustine phosphate on the antibacterial ...
P. Bergstrom+3 more
semanticscholar +1 more source
Compatibility of antineoplastic, antibiotic and corticosteroid drugs in intravenous admixtures
American Journal of Health-System Pharmacy, 1976Through the use of absorption spectroscopy and visual observations, the compatibility of selected oncologic, antibiotic and corticosteroid drugs in intravenous admixtures was determined. The six drugs used in this study were methotrexate sodium, prednisolone sodium phosphate, sodium cephalothin, 5-fluorouracil, cytarabine and vincristine sulfate. These
James C. King, MP McRae
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ChemInform Abstract: FR901228: Antineoplastic Antibiotic
ChemInform, 1999AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
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Enzymatic release of nitric oxide from L-alanosine, an antineoplastic antibiotic
Biochemical and Biophysical Research Communications, 1982Abstract L-Alanosine is an antineoplastic drug which is the 3-isonitramino analog of L -aspartic acid. The drug is known to be metabolized to the corresponding 2-oxo acid. Unlike the parent amino acid, the 2-oxo acid is unstable under mild conditions.
Theodore A. Alston, Harold J. Bright
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Daunomycin: A New Antibiotic with Antitumor Activity
Tumori Journal, 1963Daunomycin is a new antibiotic isolated from cultures of Streptomyces peucetius. For its physicochemical characteristics it may belong to the group of antibiotics described by Ollis and Sutherland (11). The toxico-pharmacologic studies of Daunomycin administered i.v. to mice and rats indicated an acute LD50 value of 15-20 mg/kg.
Gaetani M+4 more
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Preliminary Pharmacokinetics of Streptozotocin, an Antineoplastic Antibiotic
The Journal of Clinical Pharmacology, 1977A. J. Weiss+4 more
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