Zobrazeno 1 - 10
of 23
pro vyhledávání: '"John E. Schurig"'
Publikováno v:
Journal of Medicinal Chemistry. 33:2184-2188
The antitumor and DNA-binding properties of a group of oligomeric platinum(II) and platinum(IV) complexes are described. The compounds, having the stoichiometry [cis-Pt II (X) 2 (μ-OH] 2 (NO 3 ) 2 , where X is NH 3 , NH 2 CH 2 CH 3 , and NH 2 CH(CH
Publikováno v:
The Journal of Antibiotics. 43:125-127
Although rebeccamycin exhibits significant in vivo antitumor activity against P388 leukemia and B16 melanoma, its limited solubility in aqueous media posed some problems in further evaluation. In order to find more water-soluble analogues wa have car
Autor:
Dale A. Stringfellow, Hideo Kamei, John E. Schurig, Yuji Nishiyama, William C. Rose, William T. Bradner
Publikováno v:
Investigational new drugs. 8(1)
BMY-28175 is a novel antitumor antibiotic produced in fermentation by Actinomadura verrucosospora. The cytotoxic effects of BMY-28175 were determined using murine and human tumor cell lines in vitro. Following 72 hour exposure, the drug had IC50 valu
Publikováno v:
Investigational new drugs. 8
BMY-25067, N-7[2-(4-nitrophenyldithio)-ethyl] mitomycin C was selected from a number of disulfide derivatives of the highly active compound RR150, N-7(thioethyl) mitomycin C for further study. BMY-25067 had tumor inhibitory effects equivalent to mito
Publikováno v:
International Archives of Allergy and Immunology. 67:101-108
BL-5255 exhibited potent activity in several models of antigen-induced immediate hypersensitivity reactions in rats and guinea pigs. The compound was effective whether administered by oral or parenteral routes and in passively and actively sensitized
Publikováno v:
Investigational New Drugs. 7:173-178
BMY-28090 is a novel actinomycete fermentation derived antitumor agent. The cytotoxic effect of BMY-28090 was evaluated in two murine and eight human tumor cell lines in vitro. Following 72-hour exposures, BMY-28090 was cytotoxic for all of these cel
Publikováno v:
Journal of Medicinal Chemistry. 30:716-719
The synthesis and characterization of a group of platinum(IV) compounds containing the various isomeric forms of 1,2-diaminocyclohexane (DACH) are described. Antitumor tests with the new complexes, as well as with other platinum(II) compounds contain
Autor:
John E. Schurig, William C. Rose
Publikováno v:
Cancer Treatment Reviews. 12:1-19
Carboplatin, an analog of the antitumor drug Platinol, was selected for clinical evaluation on the basis of its experimental antitumor and toxicologic profile in animal models. Described in this review is a detailed summary of selected preclinical da
Autor:
William T. Bradner, John E. Schurig
Publikováno v:
Cancer Treatment Reviews. 8:93-102
Autor:
William C. Rose, Robert S. Hirth, William T. Bradner, John E. Schurig, Abraham Schlein, J B Huftalen, Alexander P. Florczyk
Publikováno v:
Cancer Chemotherapy and Pharmacology. 13:164-170
Tallysomycin S10b (TLM S10b), a structural analog of bleomycin (BLM), was evaluated and compared with BLM for antitumor activity in several murine tumor systems and for toxic effects in mice and rats. Neither TLM S10b nor BLM was effective against IP