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经验公式(希尔记法):
C8H6N2O2
化学文摘社编号:
分子量:
162.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
228-153-0
Beilstein/REAXYS Number:
383777
MDL number:
产品名称
5-硝基吲哚, 98%
InChI
1S/C8H6N2O2/c11-10(12)7-1-2-8-6(5-7)3-4-9-8/h1-5,9H
InChI key
OZFPSOBLQZPIAV-UHFFFAOYSA-N
SMILES string
[O-][N+](=O)c1ccc2[nH]ccc2c1
assay
98%
form
powder
mp
140-142 °C (lit.)
Quality Level
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Application
作为以下制备反应的反应物:
- 具有药物活性的 2-氧代-1-吡咯烷类似物
- 色氨酸双加氧酶抑制剂吡啶基-乙烯基-吲哚类化合物可作为潜在的抗癌免疫调节剂
- 蛋白激酶抑制剂和抗增殖剂
- 代谢型谷氨酸受体4(mGlu4)的正变构调节剂。
- 抗真菌剂
- 大麻素1型受体(CB1)拮抗剂
- 潜在抗癌剂
- 潜在的抗血管药
- 选择性抗白血病药
- 抗人类免疫缺陷病毒亚型1(HIV-1)的药物
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Wengen Ouyang et al.
Journal of chemical theory and computation, 16(1), 666-676 (2019-12-10)
The importance of many-body dispersion effects in layered materials subjected to high external loads is evaluated. State-of-the-art many-body dispersion density functional theory calculations performed for graphite, hexagonal boron nitride, and their heterostructures were used to fit the parameters of a
D Loakes et al.
Nucleic acids research, 23(13), 2361-2366 (1995-07-11)
3-Nitropyrrole and 5-nitroindole have been assessed as universal bases in primers for dideoxy DNA sequencing and in the polymerase chain reaction (PCR). In contrast to a previous report, we have found that the introduction of more than one 3-nitropyrrole residue
S Ball et al.
Nucleic acids research, 26(22), 5225-5227 (1998-11-04)
Studies have been carried out on the use of octamer oligonucleotides tailed with different base analogues as primers in cycle sequencing reactions. 5-Nitroindole tails improved the performance as primers of a number of octamers. A tail length of three or
Junbin Zhang et al.
Chembiochem : a European journal of chemical biology, 13(13), 1940-1945 (2012-08-14)
During the formation of RNA-induced silencing complex (RISC), the passenger and guide strand of an siRNA duplex separate from each other to generate an active RISC complex. Accumulating evidence shows that an siRNA passenger strand can also assemble into a
Caroline Crey-Desbiolles et al.
Nucleic acids research, 33(5), 1532-1543 (2005-03-16)
Universal DNA base analogs having photocleavable properties would be of great interest for development of new nucleic acid fragmentation tools. The photocleavable 7-nitroindole 2'-deoxyribonucleoside d(7-Ni) was previously shown to furnish a highly efficient approach to photochemically trigger DNA backbone cleavage
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