BMH-21
CAS No. 896705-16-1
BMH-21 ( BMH21 )
Catalog No. M16450 CAS No. 896705-16-1
BMH-21 is a RNA polymerase I inhibitor with wide and potent antitumorigenic activity across NCI60 cancer cell lines with mean GI50 of 160 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 32 | In Stock |
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10MG | 50 | In Stock |
|
25MG | 88 | In Stock |
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50MG | 149 | In Stock |
|
100MG | 259 | In Stock |
|
200MG | 389 | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
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Biological Information
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Product NameBMH-21
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NoteResearch use only, not for human use.
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Brief DescriptionBMH-21 is a RNA polymerase I inhibitor with wide and potent antitumorigenic activity across NCI60 cancer cell lines with mean GI50 of 160 nM.
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DescriptionBMH-21 is a RNA polymerase I inhibitor with wide and potent antitumorigenic activity across NCI60 cancer cell lines with mean GI50 of 160 nM, interacts with GC-Rich rDNA, potently and rapidly represses RNA polymerase I (Pol I) transcription; inhibits the expression of 47S rRNA transcript with IC50 of 60 nM, blocks transcription of the rRNA precursor without affecting rRNA maturation, and causes segregation of nucleolar proteins; causes proteasome-mediated degradation of RPA194 (Pol I catalytic subunit); activates p53 and inhibits TP53 null and mutant cell lines with GI50 of 110 and 205 nM, respectively.
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SynonymsBMH21
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PathwayCell Cycle/DNA Damage
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TargetDNA/RNA Synthesis
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RecptorRNApolymeraseI
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Research AreaCancer
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Indication——
Chemical Information
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CAS Number896705-16-1
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Formula Weight360.41
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Molecular FormulaC21H20N4O2
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESO=C(C1=CC=CN2C1=NC3C=C(C=CC=C4)C4=CC3C2=O)NCCN(C)C
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Chemical Name12H-Benzo[g]pyrido[2,1-b]quinazoline-4-carboxamide, N-[2-(dimethylamino)ethyl]-12-oxo-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Peltonen K, et al. Cancer Cell. 2014 Jan 13;25(1):77-90.
2. Colis L, et al. J Med Chem. 2014 Jun 12;57(11):4950-61.
3. Colis L, et al. Oncotarget. 2014 Jun 30;5(12):4361-9.
4. Peltonen K, et al. Mol Cancer Ther. 2014 Nov;13(11):2537-46.
2. Colis L, et al. J Med Chem. 2014 Jun 12;57(11):4950-61.
3. Colis L, et al. Oncotarget. 2014 Jun 30;5(12):4361-9.
4. Peltonen K, et al. Mol Cancer Ther. 2014 Nov;13(11):2537-46.
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