| Weight | 210.113 g/mol |
|---|---|
| Formula | C6H7FO7 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
Fluorocitrate (357-89-1)
Score:
#1240 in Neuroscience
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#2860 in Biochemistry
,
#5316 in Biology
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#7004 in Chemistry
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- An in vivo model for studying function of brain tissue temporarily devoid of glial cell metabolism: the use of fluorocitrate. (Journal of Neurochemistry, 1987)
- Use of fluorocitrate and fluoroacetate in the study of brain metabolism. (Glia, 1997)
- Selective inhibition of glial cell metabolism in vivo by fluorocitrate (Brain Research, 1992)
- Fluoroacetate and fluorocitrate: Mechanism of action (Neurochemical Research, 1991)
- Effects of the Gliotoxin Fluorocitrate on Spreading Depression and Glial Membrane Potential in Rat Brain In Situ (Journal of Neurophysiology, 1997)
- Tricarboxylic acid-cycle metabolism in brain. Effect of fluoroacetate and fluorocitrate on the labelling of glutamate aspartate, glutamine and -amino butyrate (Biochemical Journal, 1970)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(C(=O)O)C(C(C(=O)O)F)(C(=O)O)O
-
InChIKeyDGXLYHAWEBCTRU-UHFFFAOYSA-N
- Pubchem - Fluorocitrate
- Wikipedia - Fluorocitric acid
Fluorocitric acid is a fluorinated carboxylic acid derived from citric acid by substitution of one hydrogen by a fluorine atom. The appropriate anion is called fluorocitrate. Fluorocitrate is formed in two steps from Fluoroacetate.
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