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形狀
crystalline
顏色
yellow to brown
儲存溫度
2-8°C
SMILES 字串
C(Oc1ccc2cc[nH]c2c1)c3ccccc3
InChI
1S/C15H13NO/c1-2-4-12(5-3-1)11-17-14-7-6-13-8-9-16-15(13)10-14/h1-10,16H,11H2
InChI 密鑰
FPMICYBCFBLGOZ-UHFFFAOYSA-N
應用
- Reactant for enantioselective synthesis of quaternary carbon-containing 3-(3-indolyl)isoindolin-1-ones
- Reactant for Friedel-Crafts alkylation reactions with hydroxyisoindolinones
- Reactant for direct and regioselective synthesis of β-heteroarylated ketones
- Reactant for preparation of hepatitis C virus (HCV) inhibitors
- Reactant for preparation of protein kinase C (PKC) inhibitors
- Reactant for preparation of indol-3-yl tetramethylcyclopropyl ketones as CB2 cannabinoid receptor ligands
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
Nenad Manevski et al.
PloS one, 8(1), e54767-e54767 (2013-02-02)
Human UDP-glucuronosyltransferases (UGTs) are important enzymes in metabolic elimination of endo- and xenobiotics. It was recently shown that addition of fatty acid free bovine serum albumin (BSA) significantly enhances in vitro activities of UGTs, a limiting factor in in vitro-in
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