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

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Tallimustine Chemical Structure

Tallimustine Chemical Structure

CAS No. : 115308-98-0

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Description

Tallimustine (FCE 24517), a distamycin-A derivative, is an anticancer agent[1][2][4].

Cellular Effect
Cell Line Type Value Description References
L1210 IC50
208 ng/mL
Compound: 1h
Compound was tested in vitro for cytotoxicity after 48 hr of continuouse exposure against L1210 murine leukemia cells
Compound was tested in vitro for cytotoxicity after 48 hr of continuouse exposure against L1210 murine leukemia cells
10.1016/S0960-894X(97)10121-4
L1210 IC50
48.9 nM
Compound: tallimustine (TAM)
Cytotoxicity was determined after 48 hr of continuous exposure against L1210 murine leukemia cells,(cells resistant to melphalan (L-PAM)
Cytotoxicity was determined after 48 hr of continuous exposure against L1210 murine leukemia cells,(cells resistant to melphalan (L-PAM)
[PMID: 15115402]
L1210 IC50
50.3 ng/mL
Compound: 1a
Compound was tested in vitro for cytotoxicity after 48 hr of continuouse exposure against L1210 murine leukemia cells
Compound was tested in vitro for cytotoxicity after 48 hr of continuouse exposure against L1210 murine leukemia cells
10.1016/S0960-894X(97)10121-4
L1210 IC50
55.3 nM
Compound: tallimustine (TAM)
Cytotoxicity was determined after 48 hr of continuous exposure against L1210 murine leukemia cells
Cytotoxicity was determined after 48 hr of continuous exposure against L1210 murine leukemia cells
[PMID: 15115402]
In Vitro

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].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[2]

Cell Line: K562 cells
Concentration: 25 and 100 nM
Incubation Time: 4 days
Result: Inhibited cell proliferation.
In Vivo

Tallimustine (3 mg/kg, i.p.) shows antileukaemic activity in L1210 tumor bearing mice[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: L1210 tumor bearing mice[2].
Dosage: 3 mg/kg
Administration: Intraperitoneal injection (i.p.)
Result: Prolonged the survival of mice.
Clinical Trial
Molecular Weight

697.61

Formula

C32H38Cl2N10O4

CAS No.
SMILES

O=C(C1=CC=C(N(CCCl)CCCl)C=C1)NC2=CN(C)C(C(NC3=CN(C)C(C(NC4=CN(C)C(C(NCCC(N)=N)=O)=C4)=O)=C3)=O)=C2

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Room temperature in continental US; may vary elsewhere.

Storage

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

Purity & Documentation
References
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Tallimustine Related Classifications

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Tallimustine
Cat. No.:
HY-105270
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