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4-ferrocenecarboxyl-2,2,6,6-tetramethyl piperidine-1-oxyl

structure in first source

Also Known As:

FC-TEMPO

Networked: 1 relevant articles (0 outcomes, 1 trials/studies)

Bio-Agent Context: Research Results

Inorganic Chemicals: 9
- Iron Compounds: 87
  - Ferrous Compounds: 2
    - 4-ferrocenecarboxyl-2,2,6,6-tetramethyl piperidine-1-oxyl: 1
Heterocyclic Compounds: 198
- 1-Ring Heterocyclic Compounds
  - Piperidines: 17
    - 4-ferrocenecarboxyl-2,2,6,6-tetramethyl piperidine-1-oxyl: 1

Experts

1.	Han, J: 1 article (12/2006)
2.	Lan, M B: 1 article (12/2006)
3.	Li, C L: 1 article (12/2006)
4.	Liu, J W: 1 article (12/2006)
5.	Miao, L D: 1 article (12/2006)
6.	Tang, W: 1 article (12/2006)
7.	Wu, Y: 1 article (12/2006)

Related Diseases

1.	Neoplasms (Cancer) 12/01/2006 - "The cytotoxicity of FC-TEMPO in the high metastatic lung carcinoma cells (95-D) showed that it markedly inhibited the viability of cancer cells in a dose-dependent manner, while it was less toxic to a normal human cell line. " 12/01/2006 - "Further studies found that FC-TEMPO suppressed the growth of tumor cells by induced apoptosis through activating caspase-3 but not caspase-8 which was proved by caspase inhibitors, and the cell cycle arrest at G1 phase. " 12/01/2006 - "A novel nitroxide derivative, 4-ferrocenecarboxyl-2,2,6,6-tetramethyl piperidine-1-oxyl (FC-TEMPO), was synthesized for evaluating the effects of spin label compounds on tumor cells and firstly its biological effects on tumor and normal cells were evaluated. "
2.	Carcinoma (Carcinomatosis) 12/01/2006 - "The cytotoxicity of FC-TEMPO in the high metastatic lung carcinoma cells (95-D) showed that it markedly inhibited the viability of cancer cells in a dose-dependent manner, while it was less toxic to a normal human cell line. "

Related Drugs and Biologics

1.	Caspase Inhibitors
2.	Caspase 8 (Caspase-8)
3.	Caspase 3 (Caspase-3)
4.	4-ferrocenecarboxyl-2,2,6,6-tetramethyl piperidine-1-oxyl
5.	Spin Labels
6.	nitroxyl