InChI key
OLNJUISKUQQNIM-UHFFFAOYSA-N
InChI
1S/C9H7NO/c11-6-7-5-10-9-4-2-1-3-8(7)9/h1-6,10H
SMILES string
O=Cc1c[nH]c2ccccc12
grade
purum
assay
≥98.0% (T)
Application
其是制备如下化合物所需的反应物:
- 镇痛剂
- 降糖药
- 色氨酸双加氧酶抑制剂吡啶基-乙烯基-吲哚(作为潜在的抗癌免疫调节剂)
- 抗菌和抗真菌剂
- 抗变形虫药和细胞毒性剂
- 登革病毒蛋白酶的抑制剂(在细胞培养中具有抗病毒活性)
- 姜黄素类似物(可能的抗增殖 & 抗炎剂)
- Bcl-2家族蛋白的抑制剂
- RNA聚合酶IIC末端结构域的抑制剂(作为抗肿瘤剂)
- TNF-α和IL-6的抑制剂(具有抗结核活性)
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Tian-Lin Yang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 67(2), 568-571 (2006-09-22)
A new Schiff base ligand with tripodal structure, N,N',N''-tri-(3-indolemethanal)-triaminotriethylamine (L), and its complex with terbium was synthesized. The complex was characterized by element analysis, IR spectra, mass spectra, thermal analysis and molar conductivity. The terbium ion was found to coordinate
Kakul Husain et al.
European journal of medicinal chemistry, 43(9), 2016-2028 (2008-01-29)
Reaction of 3-indole carboxaldehyde with aminothiocarbonyl hydrazines resulted in the formation of 3-indole carboxaldehyde thiosemicarbazones (TSCs) 1-13. The synthesized thiosemicarbazones were used as ligands in the formation of [Pd(TSC)Cl2] complexes with palladium(II) metal ion precursor, [Pd(DMSO)2Cl2]. The chemical structures of
Anna M Vetrano et al.
The Journal of biological chemistry, 280(42), 35372-35381 (2005-08-05)
Catalase is a highly conserved heme-containing antioxidant enzyme known for its ability to degrade hydrogen peroxide into water and oxygen. In low concentrations of hydrogen peroxide, the enzyme also exhibits peroxidase activity. We report that mammalian catalase also possesses oxidase
Deepa Sinha et al.
European journal of medicinal chemistry, 43(1), 160-165 (2007-05-29)
Eight novel heterocyclic Schiff bases derived from the condensation reactions of indole 3-carboxaldehyde with different l-amino acids (histidine, glutamic acid, aspartic acid, leucine, valine) as well as with some aminophenols, have been synthesized and characterized by various spectroscopic methods (IR
S Muthu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 106, 299-309 (2013-02-19)
Indole-3-Aldehyde is a new organic non-linear material having good second harmonic generation. The optimized molecular geometry, harmonic vibrational frequencies, infrared intensities of Indole-3-Aldehyde (I3A, C9H7NO) in the ground state were carried out by using density functional theory (B3LYP) method with
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