所有图片(1)
About This Item
经验公式（希尔记法）:
C9H6N2O3
CAS号:
分子量:
190.16
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
方案
97%
表单
solid
mp
189-193 °C
官能团
aldehyde
nitro
SMILES字符串
[O-][N+](=O)c1cccc2[nH]cc(C=O)c12
InChI
1S/C9H6N2O3/c12-5-6-4-10-7-2-1-3-8(9(6)7)11(13)14/h1-5,10H
InChI key
CGXVTWQTGQAMMX-UHFFFAOYSA-N
应用
- reactant in synthesis of tryptophan dioxygenase inhibitors as potential anticancer immunomodulators
- reactant in synthesis of structural analogs of thaxtomin
- reactant in preparation of chromophores related to gold fluorescent protein
- reactant in preparation of brassinin and gramine derivatives
警示用语：
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
新产品
Prueger, Birgit; Bach, Thorsten.
Synthesis, 7, 1103-1103 (2007)
Tetrahedron, 46, 6085-6085 (1990)
Molesworth, P., P.; et al.
Australian Journal of Chemistry, 63, 813-813 (2010)
Yamada, F.; et al.
Heterocycles, 36, 2783-2783 (1993)
Eduard Dolusić et al.
Journal of medicinal chemistry, 54(15), 5320-5334 (2011-07-06)
Tryptophan catabolism mediated by indoleamine 2,3-dioxygenase (IDO) is an important mechanism of peripheral immune tolerance contributing to tumoral immune resistance. IDO inhibition is thus an active area of research in drug development. Recently, our group has shown that tryptophan 2,3-dioxygenase
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门