推薦產品
化驗
97%
形狀
solid
mp
189-193 °C
官能基
aldehyde
nitro
SMILES 字串
[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 密鑰
CGXVTWQTGQAMMX-UHFFFAOYSA-N
應用
- 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
訊號詞
Warning
危險分類
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Heterocycles, 36, 2783-2783 (1993)
Australian Journal of Chemistry, 63, 813-813 (2010)
Synthesis, 7, 1103-1103 (2007)
Tetrahedron, 46, 6085-6085 (1990)
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
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