V900750
吲哚-3-羧酸
Vetec™, reagent grade, 98%
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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关于此项目
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:
Assay:
98%
InChI
1S/C9H7NO2/c11-9(12)7-5-10-8-4-2-1-3-6(7)8/h1-5,10H,(H,11,12)
InChI key
KMAKOBLIOCQGJP-UHFFFAOYSA-N
SMILES string
OC(=O)c1c[nH]c2ccccc12
grade
reagent grade
product line
Vetec™
assay
98%
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
Legal Information
Vetec is a 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
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
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
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
A Braca et al.
Journal of natural products, 64(7), 892-895 (2001-07-28)
A new cyclohexenone (1) and a new caffeoyl ester derivative (2), together with the known compounds (-)-isolariciresinol 3-alpha-O-beta-D-glucopyranoside (3), (+)-1-hydroxypinoresinol 1-O-beta-D-glucopyranoside (4), isoacteoside (5), luteolin 4'-O-beta-D-glucopyranoside (6), and indole-3-carboxylic acid (7), were isolated from the leaves of Bauhinia tarapotensis. The
Jin-Mo Ku et al.
The Journal of organic chemistry, 72(21), 8115-8118 (2007-09-20)
An enantioselective synthetic method for (-)-cis-clavicipitic acid (1) was reported. 1 was obtained in 10 steps (99% ee and 20% overall yield) from 1H-indole-3-carboxylic acid methyl ester (9) via asymmetric phase-transfer catalytic alkylation and diastereoselective Pd(II)-catalyzed intramolecular aminocyclization as key
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