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Merck

T90301

Sigma-Aldrich

3-(2-羟乙基)吲哚

97%

别名:

2-(3-吲哚基)乙醇, 3-吲哚乙醇, IEA, NSC 3884, 色醇

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About This Item

经验公式(希尔记法):
C10H11NO
CAS号:
分子量:
161.20
Beilstein:
125553
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

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)


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Olivier Vandeputte et al.
Applied and environmental microbiology, 71(3), 1169-1177 (2005-03-05)
The role and metabolism of indole-3-acetic acid in gram-negative bacteria is well documented, but little is known about indole-3-acetic acid biosynthesis and regulation in gram-positive bacteria. The phytopathogen Rhodococcus fascians, a gram-positive organism, incites diverse developmental alterations, such as leafy
Richard Pozdrik et al.
Journal of agricultural and food chemistry, 54(17), 6123-6129 (2006-08-17)
The disappearance of riboflavin absorbance at 445 nm from beers or model beers on light exposure is directly linked to light-struck character formation. The addition of (+)-catechin, (-)-epicatechin, tryptophol, or ascorbic acid was able to reduce, but not stop, absorbance
Dina Morshedi et al.
The FEBS journal, 274(24), 6415-6425 (2007-11-22)
Amyloid aggregation of polypeptides is related to a growing number of pathologic states known as amyloid disorders. There is a great deal of interest in developing small molecule inhibitors of the amyloidogenic processes. In the present article, the inhibitory effects
Xuqing Zhang et al.
Organic letters, 7(10), 2043-2046 (2005-05-07)
The tetrahydro-pyrano[3,4-b]indoles 6 were synthesized from 2-(2-trimethylsilanyl-1H-indol-3-yl)-ethanols 5 and various ketones or aldehydes through silicon-directed oxa-Pictet-Spengler cyclizations. An unusual reaction led to the dimeric products 7 when some of 5 was treated with acetone using BF(3) as the catalyst.
Ivan Kosalec et al.
Arhiv za higijenu rada i toksikologiju, 62(1), 41-49 (2011-03-23)
Tryptophol is an aromatic alcohol and secondary metabolite of the opportunistic fungus Candida albicans. Although its toxicity profile at cell level has been poorly investigated, recent data point to cytotoxic, cytostatic, and genotoxic effects in lymphocytes and the induction of

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