Quality Level
assay
98%
form
solid
bp
157-160 °C/0.2 mmHg (lit.)
mp
33-36 °C (lit.)
functional group
nitrile
SMILES string
N#CCc1c[nH]c2ccccc12
InChI
1S/C10H8N2/c11-6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,7,12H,5H2
InChI key
DMCPFOBLJMLSNX-UHFFFAOYSA-N
General description
3-吲哚乙腈 (indolylacitrithione) 是一种光诱导的生长素抑制物质,从轻质甘蓝 ( Brassica olearea L.) 枝条中分离得到 。它抑制 大肠杆菌 O157:H7 和 铜绿假单胞菌 的生物膜形成,而不影响其生长 。
Application
反应物用于制备:
- 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
- 组蛋白脱乙酰酶抑制剂
- 潜在激酶抑制剂
- Kv7/KCNQ 钾通道激活剂
- 驱动蛋白特异性 MKLP-2 抑制剂
- 杀虫剂
- 潜在 PET 癌症显像剂
- 作为动脉粥样硬化治疗的法尼酯 X 受体 (FXR) 激动剂
- 丁酰胆碱酯酶抑制剂
- 坏死性凋亡抑制剂
存储类别
11 - Combustible Solids
flash_point_f
233.6 °F - closed cup
flash_point_c
112 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Light-induced auxin-inhibiting substance from cabbage (Brassica oleacea L.) shoots.
Kosemura S, et al.
Tetrahedron Letters, 38(48), 8327-8330 (1997)
Jin-Hyung Lee et al.
Environmental microbiology, 13(1), 62-73 (2010-07-24)
Intercellular signal indole and its derivative hydroxyindoles inhibit Escherichia coli biofilm and diminish Pseudomonas aeruginosa virulence. However, indole and bacterial indole derivatives are unstable in the microbial community because they are quickly degraded by diverse bacterial oxygenases. Hence, this work
Tongbing Su et al.
The Plant cell, 23(1), 364-380 (2011-01-18)
Camalexin, a major phytoalexin in Arabidopsis thaliana, consists of an indole ring and a thiazole ring. The indole ring is produced from Trp, which is converted to indole-3-acetonitrile (IAN) by CYP79B2/CYP79B3 and CYP71A13. Conversion of Cys(IAN) to dihydrocamalexic acid and
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 616520-10MG | 04055977185249 |
| R0658-25MG | 04061832559476 |
| R0658-5MG | 04061836693947 |
| 129453-25G | 04061832841496 |
| 129453-5G | 04061838726247 |