Tallimustine

Bioactivity Tallimustine (FCE 24517), a distamycin-A derivative, is an anticancer agent[1][2][4].
Invitro Tallimustine (0.1-10 μM, 4 h) induces damage to purified SV40 DNA[1].Tallimustine (72 h ) shows cytotoxicity in CEM Cells, with an IC50 of 3.5 nM[1].Tallimustine (25 and 100 nM, 6 days) induces erythroid differentiation of K562 cells[2].Tallimustine (100 nM, 6 days) increases accumulation of γ-globin mRNA in K562 cells[2].Tallimustine (0.5 μg/mL, 1 h) arrests SW626 cells in G2/M phase[3]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability Assay[2] Cell Line:
In Vivo Tallimustine (3 mg/kg, i.p.) shows antileukaemic activity in L1210 tumor bearing mice[4]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
Name Tallimustine
CAS 115308-98-0
Formula C32H38Cl2N10O4
Molar Mass 697.61
Transport Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Reference [1]. Herzig MC, et al. Tallimustine lesions in cellular DNA are AT sequence-specific but not region-specific. Biochemistry. 1999 Oct 19;38(42):14045-55. [2]. Bianchi N, et al. Accumulation of gamma-globin mRNA and induction of erythroid differentiation after treatment of human leukaemic K562 cells with tallimustine. Br J Haematol. 2001 Jun;113(4):951-61. [3]. Erba E, et al. Comparison of cell-cycle phase perturbations induced by the DNA-minor-groove alkylator tallimustine and by melphalan in the SW626 cell line. Int J Cancer. 1995 Jul 17;62(2):170-5. [4]. Tagliabue G, et al. Combination of the new minor groove alkylator tallimustine and melphalan. Eur J Cancer. 1997 Feb;33(2):284-7.

Tallimustine (FCE 24517), a distamycin-A derivative, is an anticancer agent.

 

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