2-amino-4-phosphonobutyric acid
2-amino-4-phosphonobutyric acid Basic information
- Product Name:
- 2-amino-4-phosphonobutyric acid
- Synonyms:
-
- 2-Amino-4-phosphonobutanoic acid
- DL-2-Amino-4-phosphonobutyric Acid, 98.0+ % (HPLC)
- Butanoic acid, 2-amino-4-phosphono-
- CAS:
- 6323-99-5
- MF:
- C4H10NO5P
- MW:
- 183.1
- Mol File:
- 6323-99-5.mol
2-amino-4-phosphonobutyric acid Chemical Properties
- Melting point:
- 229-231 °C(Solv: ethanol (64-17-5); water (7732-18-5))
- Boiling point:
- 491.7±55.0 °C(Predicted)
- Density
- 1.628±0.06 g/cm3(Predicted)
- storage temp.
- Store at RT
- solubility
- Water:9.15(Max Conc. mg/mL);50.0(Max Conc. mM)
- form
- White solid.
- pka
- 2.19±0.10(Predicted)
- color
- White to off-white
- Water Solubility
- Soluble to 50 mM in water
2-amino-4-phosphonobutyric acid Usage And Synthesis
Description
DL-AP4 is a broad-spectrum glutamatergic antagonist. DL-AP4 (2.5 mM) inhibits electrically stimulated synaptic transmission in rabbit hippocampal slices. It also depresses depolarizations induced by NMDA , L-homocysteate, or kainate in isolated frog spinal cord when used at a concentration of 1 mM. DL-AP4 (0.2 mM) inhibits the accumulation of inositol induced by ibotenate , quisqualate, L-glutamate, and L-aspartate in rat hippocampal slices.
Uses
DL-2-Amino-4-phosphonobutanoic acid (AP4) is an amino-acid derivative reported to block cone signals in the rat retina. Improves learning and memory processes in passive and active avoidance situations in rats.
storage
Store at RT
References
[1] W. FROST WHITE. Glutamate as transmitter of hippocampal perforant path[J]. Nature, 1977, 270 5635: 356-357. DOI: 10.1038/270356a0
[2] R.H. EVANS. ANTAGONISM OF EXCITATORY AMINO ACID-INDUCED RESPONSES AND OF SYNAPTIC EXCITATION IN THE ISOLATED SPINAL CORD OF THE FROG[J]. British Journal of Pharmacology, 1979, 67 4: 591-603. DOI: 10.1111/j.1476-5381.1979.tb08706.x
[3] F. NICOLETTI. Coupling of Inositol Phospholipid Metabolism with Excitatory Amino Acid Recognition Sites in Rat Hippocampus[J]. Journal of Neurochemistry, 1986, 46 1: 40-46. DOI: 10.1111/j.1471-4159.1986.tb12922.x
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