Identification | Back Directory | [Name]
HAMNO | [CAS]
138736-73-9 | [Synonyms]
HAMNO NSC111847 CID 6335338 MLS000737724 NSC111847,HAMNO HAMNO (NSC111847) HAMNO >=98% (HPLC) 2(1H)-Naphthalenone, 1-[[(2-hydroxyphenyl)amino]methylene]- HAMNO; CID 6335338; MLS000737724; NSC111847; NSC-111847; NSC111847 | [EINECS(EC#)]
604-604-1 | [Molecular Formula]
C17H13NO2 | [MOL File]
138736-73-9.mol | [Molecular Weight]
263.29 |
Chemical Properties | Back Directory | [Boiling point ]
488.8±45.0 °C(Predicted) | [density ]
1.392±0.06 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
DMF:30.0(Max Conc. mg/mL);113.94(Max Conc. mM) DMSO:30.0(Max Conc. mg/mL);113.94(Max Conc. mM) DMSO:PBS (pH 7.2) (1:30):0.25(Max Conc. mg/mL);0.95(Max Conc. mM) | [form ]
A crystalline solid | [pka]
9.98±0.35(Predicted) | [color ]
Yellow to orange |
Hazard Information | Back Directory | [Uses]
HAMNO, is a novel protein interaction inhibitor of replication protein A (RPA). It has shown to significantly inhibits colony formation when combined with etoposide. | [Biological Activity]
HAMNO is a potent and selective inhibitor of replication protein A (RPA) interactions with proteins involved in the replication stress response. HAMNO binds the N-terminal domain of RPA70 and inhibits both ATR autophosphorylation and phosphorylation of RPA32 Ser33 by ATR. HAMNO enhances DNA replication stress in cancer cells and slow tumor growth in vivo. | [in vivo]
In mice, HAMNO slows the progression of UMSCC11B tumors. Ser33 of RPA32, an ATR substrate, is highly phosphorylated after two hours of treatment with 20 μM of etoposide, which is reduced with the addition of 2 μM HAMNO, and is nearly absent at higher concentrations, demonstrating an in vivo effect of HAMNO as an inhibitor of RPA32 phosphorylation by ATR[1]. | [storage]
Store at -20°C |
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Company Name: |
Twochem Co.Ltd.
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Tel: |
021-58111628 15800915896 |
Website: |
cn.twochem.com |
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