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Key Documents

N1537

Sigma-Aldrich

NU7026

≥98% (HPLC), solid

同義詞:

2-(吗啉-4-基)-苯并[h]铬-4-酮

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About This Item

經驗公式(希爾表示法):
C17H15NO3
CAS號碼:
分子量::
281.31
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

品質等級

化驗

≥98% (HPLC)

形狀

solid

顏色

tan

溶解度

DMSO: soluble 3 mg/mL at 60 °C
H2O: insoluble

運輸包裝

wet ice

儲存溫度

2-8°C

SMILES 字串

O=C1C=C(Oc2c1ccc3ccccc23)N4CCOCC4

InChI

1S/C17H15NO3/c19-15-11-16(18-7-9-20-10-8-18)21-17-13-4-2-1-3-12(13)5-6-14(15)17/h1-6,11H,7-10H2

InChI 密鑰

KKTZALUTXUZPSN-UHFFFAOYSA-N

應用

NU7026 已用于:
  • 作为 DNA 依赖性蛋白激酶(DNA-PK)抑制剂,用于治疗结肠癌细胞
  • 在激酶抑制剂实验中,用于处理在 20 h-人绒毛膜促性腺激素(hCG)后原核可见的受精卵
  • 确定其对 dibenzo[def,p]chrysene 处理 HepG2 细胞的细胞毒性的影响

有效的,ATP 竞争。IC50 = 0.23 μM。对其他 PI3K 相关激酶的选择性(对于 PI3K,IC50 = 13 μM,对于 ATM 和 ATR 为 >100 μM)。

生化/生理作用

细胞可透过性 DNA-PK(DNA 依赖性蛋白激酶)小分子 benzochromenone 抑制剂。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


分析證明 (COA)

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Takeshi Yasuda et al.
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SIRT2 and SIRT3 protein deacetylases maintain genome integrity and stability. However, their mechanisms for maintaining the genome remain unclear. To examine the roles of SIRT2 and SIRT3 in DSB repair, I-SceI-based GFP reporter assays for HR, single-strand annealing (SSA) and
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Cancers, 11(9) (2019-09-05)
Uveal melanoma (UM) is the most common primary intraocular tumour in adults, with a mean survival of six months following metastasis. The survival rates have not improved in over 30 years. This study has shown that sister chromatid exchange (SCE)
The influence of ATM, ATR, DNA-PK inhibitors on the cytotoxic and genotoxic effects of dibenzo [def, p] chrysene on human hepatocellular cancer cell line HepG2
Spryszynska S, et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis, 791, 12-24 (2015)
Sandra Wimberger et al.
Nature communications, 14(1), 4761-4761 (2023-08-15)
Genome editing, specifically CRISPR/Cas9 technology, has revolutionized biomedical research and offers potential cures for genetic diseases. Despite rapid progress, low efficiency of targeted DNA integration and generation of unintended mutations represent major limitations for genome editing applications caused by the
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PloS one, 6(12), e28756-e28756 (2011-12-24)
Non-homologous end joining (NHEJ) is a major pathway for the repair of DNA double strand break (DSBs) with incompatible DNA ends, which are often generated by ionizing irradiation. In vitro reconstitution studies have indicated that NHEJ of incompatible DNA ends

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