Identification | Back Directory | [Name]
BMH21 | [CAS]
896705-16-1 | [Synonyms]
BMH21 CS-1749 BMH 21;BMH21 BMH-21, >98% BMH21 USP/EP/BP N-[2-(Dimethylamino)ethyl]-12-oxo-5,13-diazatetracene-4-carboxamide N-[2-(Dimethylamino)ethyl]-12-oxo-2H-benzo[g]pyrido[2,1-b]quinazoline-4-carboxamide N-[2-(dimethylamino)ethyl]-12-oxo-12H-benzo[g]pyrido[2,1-b]quinazoline-4-carboxamide 12H-Benzo[g]pyrido[2,1-b]quinazoline-4-carboxamide, N-[2-(dimethylamino)ethyl]-12-oxo- BMH-21 N-[2-(Dimethylamino)ethyl]-12-oxo-12H-benzo[g]pyrido[2,1-b]quinazoline-4-carboxamide | [EINECS(EC#)]
809-833-1 | [Molecular Formula]
C21H20N4O2 | [MDL Number]
MFCD27225377 | [MOL File]
896705-16-1.mol | [Molecular Weight]
360.41 |
Chemical Properties | Back Directory | [density ]
1.28±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
DMSO: soluble1mg/mL, clear (warmed) | [form ]
powder | [pka]
7.90±0.20(Predicted) | [color ]
light yellow to dark yellow |
Hazard Information | Back Directory | [Uses]
BMH-21 has been used in cell culture. | [General Description]
BMH-21 is a planar heterocyclic small molecule DNA intercalator. | [Biochem/physiol Actions]
BMH-21 is a potent inhibitor of RNA Pol I. BMH-21 binds strongly to GC-rich DNA sequences, ultimately inhibiting RNA Pol I, blocking transcription and disrupting the nucleolar structure. BMH-1 causes dissociation of the RPA194 catalytic subunit from Pol I, and disassembly of Pol I:DNA complexes. The compound BMH-21 inhibits proliferation of a broad range of tumor cell lines. | [storage]
Store at -20°C |
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Company Name: |
BOC Sciences
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1-631-485-4226; 16314854226 |
Website: |
https://www.bocsci.com |
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