1. Cell Cycle/DNA Damage Cytoskeleton Apoptosis
  2. Microtubule/Tubulin Apoptosis
  3. MPT0B002

MPT0B002 is a potent microtubule inhibitor with anticancer activities. MPT0B002 disrupts tubulin polymerization, induces apoptosis, and arrests cell cycle at the G2/M phase.

For research use only. We do not sell to patients.

MPT0B002 Chemical Structure

MPT0B002 Chemical Structure

CAS No. : 946077-08-3

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Description

MPT0B002 is a potent microtubule inhibitor with anticancer activities. MPT0B002 disrupts tubulin polymerization, induces apoptosis, and arrests cell cycle at the G2/M phase[1].

Cellular Effect
Cell Line Type Value Description References
A549 IC50
0.12 μM
Compound: XIII
Cytotoxicity against human A549 cells after 72 hrs by XTT assay
Cytotoxicity against human A549 cells after 72 hrs by XTT assay
[PMID: 19939521]
A549 IC50
0.12 μM
Compound: 4d
Cytotoxicity against human A549 cells after 72 hrs by XTT assay
Cytotoxicity against human A549 cells after 72 hrs by XTT assay
[PMID: 19647439]
A549 IC50
0.12 μM
Compound: 7
Cytotoxicity against human A549 cells after 72 hrs by XTT method
Cytotoxicity against human A549 cells after 72 hrs by XTT method
[PMID: 18502133]
A549 IC50
190 nM
Compound: 4
Cytotoxicity against human A549 cells assessed as growth inhibition after 72 hrs by XTT assay
Cytotoxicity against human A549 cells assessed as growth inhibition after 72 hrs by XTT assay
[PMID: 23470139]
HeLa IC50
0.034 μM
Compound: XIII
Cytotoxicity against human HeLa cells after 72 hrs by XTT assay
Cytotoxicity against human HeLa cells after 72 hrs by XTT assay
[PMID: 19939521]
HeLa IC50
0.034 μM
Compound: 7
Cytotoxicity against human HeLa cells after 72 hrs by XTT method
Cytotoxicity against human HeLa cells after 72 hrs by XTT method
[PMID: 18502133]
HeLa IC50
0.035 μM
Compound: 4d
Cytotoxicity against human HeLa cells after 72 hrs by XTT assay
Cytotoxicity against human HeLa cells after 72 hrs by XTT assay
[PMID: 19647439]
HeLa IC50
25 nM
Compound: 4
Cytotoxicity against human HeLa cells assessed as growth inhibition after 72 hrs by XTT assay
Cytotoxicity against human HeLa cells assessed as growth inhibition after 72 hrs by XTT assay
[PMID: 23470139]
HL-60 IC50
27 nM
Compound: 4
Cytotoxicity against human HL60 cells assessed as growth inhibition after 72 hrs by XTT assay
Cytotoxicity against human HL60 cells assessed as growth inhibition after 72 hrs by XTT assay
[PMID: 23470139]
HT-29 IC50
10.5 nM
Compound: 14
Growth inhibition of human HT29 cells after 72 hrs by methylene blue dye assay
Growth inhibition of human HT29 cells after 72 hrs by methylene blue dye assay
[PMID: 17685504]
HT-29 IC50
27 nM
Compound: 4
Cytotoxicity against human HT-29 cells assessed as growth inhibition after 72 hrs by XTT assay
Cytotoxicity against human HT-29 cells assessed as growth inhibition after 72 hrs by XTT assay
[PMID: 23470139]
KB IC50
13.6 nM
Compound: 14
Growth inhibition of human KB cells after 72 hrs by methylene blue dye assay
Growth inhibition of human KB cells after 72 hrs by methylene blue dye assay
[PMID: 17685504]
MKN-45 IC50
11.2 nM
Compound: 14
Growth inhibition of human MKN45 cells after 72 hrs by methylene blue dye assay
Growth inhibition of human MKN45 cells after 72 hrs by methylene blue dye assay
[PMID: 17685504]
NCI-H460 IC50
14.1 nM
Compound: 14
Growth inhibition of human H460 cells after 72 hrs by methylene blue dye assay
Growth inhibition of human H460 cells after 72 hrs by methylene blue dye assay
[PMID: 17685504]
TSGH IC50
13.4 nM
Compound: 14
Growth inhibition of human TSGH cells after 72 hrs by methylene blue dye assay
Growth inhibition of human TSGH cells after 72 hrs by methylene blue dye assay
[PMID: 17685504]
In Vitro

MPT0B002 (1-1000 nM; 48 h) induces G2/M-phase cell cycle arrest[1].
MPT0B002 (100 nM; 24 h) inhibits cell viability in a dose-dependent manner in K562, BaF3/p210, and BaF3/T315I cells[1].
MPT0B002 (100 nM; 48 h) induces apoptosis and can downregulate both Bcr-Abl and Bcr-Abl-T315I mRNA expressions and protein levels and the downstream signaling pathways[1].

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

Cell Viability Assay[1]

Cell Line: K562, BaF3/p210, and BaF3/T315I cells
Concentration: 1 nM, 10 nM, 100 nM, 1000 nM
Incubation Time: 48 h
Result: Inhibited cell viability in a dose-dependent manner.

Cell Cycle Analysis[1]

Cell Line: K562, BaF3/p210, and BaF3/T315I cells
Concentration: 100 nM
Incubation Time: 24 h
Result: Induced G2/M-phase cell cycle arrest.

Apoptosis Analysis[1]

Cell Line: K562, BaF3/p210, and BaF3/T315I cells
Concentration: 100 nM
Incubation Time: 48 h
Result: Induced apoptosis and caspase-3 pathway.

Western Blot Analysis[1]

Cell Line: K562, BaF3/p210, and BaF3/T315I cells
Concentration: 100 nM
Incubation Time: 48 h
Result: Significantly reduced the expression level of Bcr-Abl, and reduced the phosphorylations of Crkl and Stat5.
Molecular Weight

325.36

Formula

C19H19NO4

CAS No.
SMILES

O=C(C1=CC(OC)=C(C(OC)=C1)OC)C2=CC3=C(C=C2)N(C=C3)C

Shipping

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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Product Name:
MPT0B002
Cat. No.:
HY-122151
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