* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
cytolytic compounds such as: bleomycin, dacarbazine, hydroxycarbamide, asparaginase, mitoguazone, plicamycin,
is administered intravenously as in Test Procedure A, supra, in conjunction with a chemotherapeutic amount of one of the following antineoplastic agents capable of causing emesis: dacarbazine, nitrogen mustard, cyclophosphamide, dactinomycin, 6-thioguanidine, carmustine, lomustine, methotrexate, 5-fluorouracil, ...
Chemotherapeutic agents that are bound to monoclonal antibodies of the present invention to drive the cytotoxic activity include the following: ... carboplatin, cladribine, cyclophosphamide, cytarabine, dacarbazine, docetaxel, dactinomycin, daunomycin glucuronide, ...
Illustrative examples of chemotherapeutic agents which may be conjugated with the antibody of the invention and have a cytotoxic effect include: ... carboplatin, cladribine, cyclophosphamide, cytarabine, dacarbazine, docetaxel, dactinomycin, daunomycin glucuronide, ...
take 378 mg (3.0 mmol) of 5-amino-4-imidazolecarboxamide in a 50 mL round bottom flask, add 1.0 mL of distilled water and stir in an ice bath; take 1.2 mL (about 12.0 mmol) of concentrated hydrochloric acid and use After diluting with 2.0mL of water, it was slowly added to the reaction flask. The reaction was always carried out in an ice bath. 207mg (3.0mmol) of sodium nitrite (NaNO2) was dissolved in 1.0mL of distilled water and slowly added to the reaction system. Potassium starch iodide Test strips confirmed the excess of sodium nitrite during the reaction. At this time, the reaction solution turned dark red, and the reaction was always performed under an ice bath. After stirring for 0.5 h, 0.5 mL (4.5 mmol) of an aqueous solution containing 40% dimethylamine was added dropwise to the reaction system, and the reaction was continued at a low temperature for 2 h. After completion of the reaction, the reaction solution was lyophilized. The lyophilized residue was dissolved in water and passed through a solid-phase chromatography column and a 0.25 mum filter membrane. The sample was purified by RP-HPLC [eluent: V (methanol): V (water) = 15: 85]. The fractions were combined and the temperature was low. The methanol was removed by rotary evaporation, and the residual liquid was lyophilized to obtain 415 mg of a pale red solid powder with a yield of 76.2%.