Bisantrene is a highly effective antitumor agent, it exerts its cytotoxicity by affecting DNA intercalation. Bisantrene targets eukaryotic typeII topoisomerases. Bisantrene is a substrate of MDR1^[1][2][3][4].

Bisantrene promots DNase I cleavage at oligopurine-oligopyrimidine tracts and slightly reduces the cleavage activity at alternating purine-pyrimidine sequences^[1].
Bisantrene is an inhibitor of [³H]uridine incorporation into RNA and [³H]thymidine incorporation into DNA^[2].

Bisantrene is an antitumor agent active against a number of experimental tumors, including P388 leukemia, L1210 leukemia, Lieberman plasma cell tumor, B16 melanoma, colon tumor 26, and Ridgway osteogenic sarcoma^[3].
Bisantrene is effective over a dose range of 1.56 to 150 mg/kg depending upon the frequency, route, and schedule of the treatment and the tumor model used^[3].
Bisantrene (25, 50 and 100 mg/kg; i.p.; once) pretreats with macrophages shows antitumor effect to mice with P815 tumor cells injection^[3].
Bisantrene (10-150 mg/kg; i.v.; once) dose-dependently induces leukopenia in Neo mice. B cells and macrophages are targets for bisantrene toxicity^[4].

398.46

Solid

C₂₂H₂₂N₈

78186-34-2

比生群；必桑郡

Room temperature in continental US; may vary elsewhere.

DMSO : 1 mg/mL(2.51 mM;ultrasonic and warming and heat to 80℃)

H₂O : 0.1 mg/mL(0.25 mM;ultrasonic and warming and heat to 50℃)

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