推薦產品
化驗
97%
mp
56-59 °C (lit.)
SMILES 字串
OCCc1c[nH]c2ccccc12
InChI
1S/C10H11NO/c12-6-5-8-7-11-10-4-2-1-3-9(8)10/h1-4,7,11-12H,5-6H2
InChI 密鑰
MBBOMCVGYCRMEA-UHFFFAOYSA-N
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應用
作为反应物用于制备:
- RNA聚合酶ⅡC末端结构域抑制剂及其抗肿瘤活性
- 抗-HIV-1试剂
- 蛋白质与蛋白质的相互作用的抑制剂
- 羟色胺5-HT1A受体的部分激动剂
- 生长激素促分泌剂
- 血管内皮生长因子(VEGF)抑制剂
- A2B腺苷受体配体
- 十字花科植物抗毒素黄铜素的潜在解毒抑制剂
- 白细胞介素6抑制剂
- 双重结合位点乙酰胆碱酯酶抑制剂
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)
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’.。
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Rhizobacteria isolated from wild dipterocarp saplings in Central Kalimantan, Indonesia, were subjected to Salkowski's reagent test, which is often used in detecting indolic substances. Among 69 isolates grown in a low-nitrogen medium supplemented with L-tryptophan (TRP), culture fluids of 29
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Reduction of ketosulfonyl indoles with sodium borohydride provides a ready entry to tryptophols in a regiocomplementary fashion with respect to the traditional oxirane ring-opening by indoles under Friedel-Crafts conditions. Compared to traditional β-ketosulfones, ketosulfonyl indoles show a peculiar behavior since
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