跳轉至內容
Merck
全部照片(1)

Key Documents

SML1540

Sigma-Aldrich

SBI-0206965

≥98% (HPLC)

同義詞:

2-((5-溴-2-((3,4,5-三甲氧基苯基)氨基)嘧啶-4-基)氧)-N-甲基苯甲酰胺

登入查看組織和合約定價


About This Item

經驗公式(希爾表示法):
C21H21BrN4O5
CAS號碼:
分子量::
489.32
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

powder

顏色

white to beige

溶解度

DMSO: 20 mg/mL, clear

儲存溫度

−20°C

SMILES 字串

BrC1=C(OC2=C(C(NC)=O)C=CC=C2)N=C(NC3=CC(OC)=C(OC)C(OC)=C3)N=C1

InChI

1S/C21H21BrN4O5/c1-23-19(27)13-7-5-6-8-15(13)31-20-14(22)11-24-21(26-20)25-12-9-16(28-2)18(30-4)17(10-12)29-3/h5-11H,1-4H3,(H,23,27)(H,24,25,26)

InChI 密鑰

NEXGBSJERNQRSV-UHFFFAOYSA-N

應用

SBI-0206965已用于研究其对镉转化的前列腺上皮细胞生长的影响。

生化/生理作用

SBI-0206965 是丝氨酸/苏氨酸自噬起始激酶 ULK1 和 ULK2 的强效选择性抑制剂,对 ULK1 具有选择性。 SBI-0206965对于ULK1的IC50值为108 nM,而对于ULK2为711 nM。 肿瘤细胞需要自噬来清除错误折叠的蛋白质或受损的细胞器。SBI-0206965可抑制mTOR抑制诱导的细胞自噬。 mTOR信号通常在许多肿瘤中过度活跃,并能驱动增殖,所以mTOR抑制剂作为抗癌药物正在被研究。 然而,mTOR抑制也会导致激活依赖于ulk1的自噬生存反应,而mTOR抑制剂的大多数结果最多只能起到细胞抑制作用。 SBI-0206965协同mTOR抑制诱导细胞凋亡和死亡。
由于大多数肿瘤细胞通过自噬机制存活,因此抑制自噬诱导物Unc-51(丝氨酸/苏氨酸蛋白激酶)样自噬激活激酶(ULK1和ULK2)可能在癌症治疗中有用。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

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


分析證明 (COA)

輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。

已經擁有該產品?

您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

Structure and function of the ULK1 complex in autophagy.
Lin M G and James H H
Current Opinion in Cell Biology, 39, 61-68 (2016)
Venkatesh Kolluru et al.
Cancer letters, 408, 121-129 (2017-08-29)
Chronic exposure to cadmium is known to be a risk factor for human prostate cancer. Despite over-whelming evidence of cadmium causing carcinogenicity in humans, the specific underlying molecular mechanisms that govern metal-induced cellular transformation remain unclear. Acute exposure (up to
Cansu Karabiyik et al.
STAR protocols, 2(4), 100926-100926 (2021-11-13)
The regulation of lipid kinases has remained elusive given the difficulties of assessing changes in lipid levels. Here, we describe the isolation of protein and lipid kinases to determine the regulation of lipid kinases in vitro. This can be followed
Séverine Olivier et al.
International journal of molecular sciences, 20(20) (2019-10-23)
The AMP-activated protein kinase (AMPK) is principally known as a major regulator of cellular energy status, but it has been recently shown to play a key structural role in cell-cell junctions. The aim of this study was to evaluate the
Yuji Tanaka et al.
Scientific reports, 9(1), 18694-18694 (2019-12-12)
Metformin is used to treat type 2 diabetes. Metformin activates AMP-activated kinase (AMPK), which may contribute to the action of metformin. Metformin also shows anti-proliferation activity. However, the mechanism is remained unknown. We found that treatment of MCF-7 cells with

我們的科學家團隊在所有研究領域都有豐富的經驗,包括生命科學、材料科學、化學合成、色譜、分析等.

聯絡技術服務