推薦產品
化驗
≥95%
形狀
solid
mp
255-260 °C
儲存溫度
2-8°C
SMILES 字串
OB(O)c1cncc(Cl)c1
InChI
1S/C5H5BClNO2/c7-5-1-4(6(9)10)2-8-3-5/h1-3,9-10H
InChI 密鑰
NJXYBTMCTZAUEE-UHFFFAOYSA-N
應用
5-Chloro-3-pyridineboronic acid can be used as an intermediate:
- In the preparation of positron emission tomography (PET) radioligand [11C]MK-1064, which is applicable in the orexin-2 receptor imaging.
- In the synthesis of orexin 2 receptor antagonist (2-SORA) MK-1064.
- In the preparation of pyridyl-cycloalkyl derived microsomal prostaglandin E synthase-1 inhibitors.
- In the synthesis of ATAD2 bromodomain inhibitors.
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’.。
Discovery and optimization of pyridyl-cycloalkyl-carboxylic acids as inhibitors of microsomal prostaglandin E synthase-1 for the treatment of endometriosis
Bioorganic & Medicinal Chemistry Letters, 29(18), 2700-2705 (2019)
Fragment-based discovery of low-micromolar ATAD2 bromodomain inhibitors
Journal of Medicinal Chemistry, 58(14), 5649-5673 (2015)
Synthesis of [11C] MK-1064 as a new PET radioligand for imaging of orexin-2 receptor
Bioorganic & Medicinal Chemistry Letters, 26(15), 3694-3699 (2016)
Discovery of 5″-Chloro-N-[(5,6-dimethoxypyridin-2-yl) methyl]-2, 2′: 5′, 3″-terpyridine-3′-carboxamide (MK-1064): A Selective Orexin 2 Receptor Antagonist (2-SORA) for the Treatment of Insomnia
ChemMedChem, 9(2), 311-322 (2014)
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