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Merck
CN

57225

吲哚-3-羧酸

purum, ≥98.0% (T)

别名:

β-吲哚羧酸, 3-吲哚甲酸, 3-吲哚羧酸, 3-羧基吲哚, 吲哚-β-羧酸

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经验公式(希尔记法):
C9H7NO2
化学文摘社编号:
分子量:
161.16
EC Number:
212-231-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
129435
MDL number:
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InChI key

KMAKOBLIOCQGJP-UHFFFAOYSA-N

InChI

1S/C9H7NO2/c11-9(12)7-5-10-8-4-2-1-3-6(7)8/h1-5,10H,(H,11,12)

SMILES string

OC(=O)c1c[nH]c2ccccc12

grade

purum

assay

≥98.0% (T)

mp

232-234 °C (dec.) (lit.)

Application

作为反应物用于制备:
  • 抗癌剂
  • 氨基酸和肽的衍生物
  • 5-羟色胺5-HT4受体拮抗剂
  • 主要的酰基脲类
  • 在Hedgehog途径中,Gli1介导的转录的抑制剂
  • 5-羟色胺5-HT6拮抗剂
  • 超晚期抗原-4(VLA-4)拮抗剂
  • EphB3受体酪氨酸激酶抑制剂
  • 阿尔茨海默病的潜在治疗药物
  • 乙烯基酯假三肽蛋白酶体抑制剂

法规信息

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Toyokazu Yoshida et al.
Bioscience, biotechnology, and biochemistry, 66(11), 2388-2394 (2003-01-01)
After enrichment culture with indole-3-carboxylate in static culture, a novel reversible decarboxylase, indole-3-carboxylate decarboxylase, was found in Arthrobacter nicotianae FI1612 and several molds. The enzyme reaction was examined in resting-cell reactions with A. nicotianae FI1612. The enzyme activity was induced
Paweł Bednarek
Current opinion in plant biology, 15(4), 407-414 (2012-03-27)
In plants, a host's responses to an attempted infection include activation of various secondary metabolite pathways, some of which are specific for particular plant phylogenetic clades. Phytochemicals that represent respective end products in plant immunity have been stereotypically linked to
J J Michnovicz et al.
Journal of the National Cancer Institute, 82(11), 947-949 (1990-06-06)
Dietary indoles in cruciferous vegetables induce cytochrome P450 enzymes and have prevented tumors in various animal models. Because estradiol metabolism is also cytochrome P450 mediated and linked to breast cancer risk, indoles may similarly reduce estrogen-responsive tumors in humans. We
M U Ahmad et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 23(9), 841-847 (1985-09-01)
The nitrosation of gramine, a tertiary amine alkaloid present in barley malt, was carried out by reaction with sodium nitrite in buffered acetic acid (pH 3.4) for 1 hr at room temperature. Two major non-volatile products of the nitrosation reaction
J Hagemeier et al.
Proceedings of the National Academy of Sciences of the United States of America, 98(2), 753-758 (2001-01-03)
The chemical structures and accumulation kinetics of several major soluble as well as wall-bound, alkali-hydrolyzable compounds induced upon infection of Arabidopsis thaliana leaves with Pseudomonas syringae pathovar tomato were established. All identified accumulating products were structurally related to tryptophan. Most

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