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Merck
CN

220027

3-吲哚丙酸

ReagentPlus®, 99%

别名:

3-(3-吲哚基)丙酸, IPA, NSC 3252, NSC 47831, 吲哚-3-丙酸

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关于此项目

经验公式(希尔记法):
C11H11NO2
化学文摘社编号:
分子量:
189.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-600-1
Beilstein/REAXYS Number:
147733
MDL number:
Assay:
99%
Form:
powder
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product line

ReagentPlus®

assay

99%

form

powder

mp

134-135 °C (lit.)

solubility

ethanol: soluble 50 mg/mL, clear, yellow to orange

functional group

carboxylic acid

SMILES string

OC(=O)CCc1c[nH]c2ccccc12

InChI

1S/C11H11NO2/c13-11(14)6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,7,12H,5-6H2,(H,13,14)

InChI key

GOLXRNDWAUTYKT-UHFFFAOYSA-N

General description

3-吲哚丙酸是错误折叠的β-淀粉样蛋白(Abeta)聚集的一种有效抑制剂。通过三组分一锅法进行3-吲哚丙酸的组装已被报道

Application

反应物用于制备:
  • 独脚金内酯的荧光类似物
  • 抗肿瘤剂
  • 黑皮质素受体配体
  • 免疫抑制剂
  • 丙肝病毒抑制剂
  • 组胺H4受体激动剂
  • NR2B/NMDA受体拮抗剂
  • CB1拮抗剂用于治疗肥胖症免疫抑制剂
  • 抗细菌剂
  • TGF-β受体结合抑制剂

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Xun Cheng et al.
Analytical chemistry, 77(21), 7012-7015 (2005-11-01)
Alzheimer's disease is the most common cause of the loss of cognitive function among the elderly, and the aggregation and deposition of misfolded beta-amyloid protein (Abeta) contribute to this progressive central nervous system decline. Therefore, compounds that inhibit or even
Mauro F A Adamo et al.
Organic letters, 9(2), 303-305 (2007-01-16)
A three-component one-pot procedure (3-MC) was developed to assemble 3-indolepropionic acids from commercially available materials. This new methodology affords the title compounds in high yields and without the use of chromatography. [reaction: see text].
F Mandelbaum-Shavit et al.
Antimicrobial agents and chemotherapy, 35(12), 2526-2530 (1991-12-01)
Indole-3-propionic acid (IPA), a phytohormone derivative, is a potent inhibitor of growth of Legionella pneumophila cultivated extracellularly in a chemically defined hypotonic medium and intracellularly in human monocytes. The inhibitory activity turns into bactericidal activity with increasing concentrations. The susceptibility



全球贸易项目编号

货号GTIN
220027-1G04061838776198
220027-10G04061838776181