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HAMNO

    
≥98%

HAMNO

源叶(MedMol)
S87735 一键复制产品信息
138736-73-9
C17H13NO2
263.29062
HAMNO; CID 6335338, MLS000737724, NSC111847, NSC-111847; NSC111847
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S87735-5mg
≥98%

¥180.00

6 - - - -
S87735-10mg
≥98%

¥250.00

7 - - - -
S87735-25mg
≥98%

¥430.00

8 - - - -
S87735-100mg
≥98%

¥1040.00

2 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: HAMNO is a novel protein interaction inhibitor of replication protein A (RPA).
靶点: RPA;DNA/RNASynthesis
体外研究: HAMNO is a novel protein interaction inhibitor of replication protein A (RPA). RPA is involved in the ATR/Chk1 pathway. HAMNO alone inhibits colony formation in both HNSCC cell lines in the low micromolar range. HAMNO combined with etoposide significantly inhibits colony formation to a greater degree than HAMNO alone. After UMSCC38 cells are exposed to HAMNO, increased pan-nuclear γ-H2AX staining occurs in a dose dependent manner. Cancer derived UMSCC38 cells, as well as another cancer cell line, UMSCC11B, have prominent γ-H2AX staining, particularly after incubation with 20 μM HAMNO. Both UMSCC38 and OKF4 cells present increased γ-H2AX staining after addition of HAMNO, with the greatest increase in signal occurring in S-phase.
体内研究: 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.
参考文献: 1. Glanzer JG, et al. RPA inhibition increases replication stress and suppresses tumor growth. Cancer Res. 2014 Sep 15;74(18):5165-72.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.798 ml 18.99 ml 37.981 ml
5 mM 0.76 ml 3.798 ml 7.596 ml
10 mM 0.38 ml 1.899 ml 3.798 ml
50 mM 0.076 ml 0.38 ml 0.76 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

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