1. Cell Cycle/DNA Damage Others
  2. Topoisomerase Others
  3. MSN8C

MSN8C, an analog of mansonone E, is a novel catalytic inhibitor of human DNA topoisomerase II. MSN8C induces cancer cell apoptosis. MSN8C shows significant anti-tumor cell proliferation activity in vitro.

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MSN8C Chemical Structure

MSN8C Chemical Structure

CAS No. : 1314798-31-6

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Description

MSN8C, an analog of mansonone E, is a novel catalytic inhibitor of human DNA topoisomerase II. MSN8C induces cancer cell apoptosis. MSN8C shows significant anti-tumor cell proliferation activity in vitro[1].

Cellular Effect
Cell Line Type Value Description References
CNE-2 IC50
2.05 μM
Compound: 7
Antitumor against human CNE2 cells assessed as cell survival after 48 hrs by MTT assay
Antitumor against human CNE2 cells assessed as cell survival after 48 hrs by MTT assay
[PMID: 21600681]
In Vitro

MSN8C prevents supercoiled DNA from entering the catalytic cycle to avoid capture by Topo II poisons and reduces fragmented DNA generation[1].
MSN8C (1-10 μM, 24 h) induces HL-60 cancer cell apoptosis via increases caspases-3 expression in a dose-dependent manner.[1].
MSN8C (1, 5, 10, 20 μM, 12 h) increases caspase-8 and caspase-9 activity in HL-60 cells[1].
MSN8C (48 h) inhibits human 11 tumor cell lines from various origins with an average IC50 value of 2.6 µM[1].
MSN8C has strong antiproliferative effects on the human breast cancer adriamycin (HY-15142)-resistant cell line MCF-7/Adr and mitoxantrone (HY-13502)-resistant cell line HL-60/MX2[1].

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

Western Blot Analysis[1]

Cell Line: HL-60 cells
Concentration: 10 μM
Incubation Time: 1 h
Result: Reduced γ-H2AX expression levels.
Weakened the production of γ-H2AX by VP-16.

Western Blot Analysis[1]

Cell Line: HL-60 cells
Concentration: 1, 5, 10, 20 μM
Incubation Time: 1, 5, 10, 20 μM
Result: Induced caspases-3 express in a dose-dependent manner.

Apoptosis Analysis[1]

Cell Line: HL-60 cells
Concentration: 5, 10 μM
Incubation Time: 12 h
Result: Promoted caspase-8 and caspase-9 activity in a dose-dependent manner.
In Vivo

MSN8C (10 mg/kg, i.p, two-day intervals for 2 weeks) in a A549 tumor xenograft model inhibits tumor growth with less toxic[1].

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

Animal Model: A549 tumor xenograft model, female BALB/c nude mice[1]
Dosage: 10 mg/kg
Administration: Intraperitoneal injection (i.p.), two-day intervals for 2 weeks
Result: Inhibits tumor with the tumor weight inhibition (TWI) value of 74.2%.
Molecular Weight

214.22

Formula

C13H10O3

CAS No.
SMILES

CC(CO1)C2=C(C1=CC(C3=O)=O)C3=CC=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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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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MSN8C
Cat. No.:
HY-149410
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