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| | CIS-4-[PHOSPHONOMETHYL]-PIPERIDINE-2-CARBOXYLIC ACID Basic information |
| | CIS-4-[PHOSPHONOMETHYL]-PIPERIDINE-2-CARBOXYLIC ACID Chemical Properties |
| Melting point | 290-292 °C | | Boiling point | 508.6±60.0 °C(Predicted) | | density | 1.440±0.06 g/cm3(Predicted) | | storage temp. | Store at RT | | solubility | H2O: soluble | | form | solid | | pka | 2.29±0.10(Predicted) | | color | white | | Water Solubility | Soluble to 25 mM in water |
| | CIS-4-[PHOSPHONOMETHYL]-PIPERIDINE-2-CARBOXYLIC ACID Usage And Synthesis |
| Uses | CGS 19755 is a potent and competitive NMDA antagonist. | | Definition | ChEBI: Selfotel is a non-proteinogenic alpha-amino acid. | | Biological Activity | Potent, competitive NMDA receptor antagonist. Anticonvulsant and neuroprotective. Also available as part of the Mixed NMDA Receptor Tocriset™ . | | in vivo | Selfotel (CGS 19755) administered p.o. by gavage has little or no effect in these test procedures. In an experimental model of anxiety in rats[1].
Selfotel (CGS 19755) significantly increases conflict responding within a relatively narrow dose range (minimum effective dose, 1.73 mg/kg i.p.)[1].
Selfotel (CGS 19755) blocks the harmaline-induced increase in cerebellar cyclic GMP levels at a dose of 4 mg/kg i.p. with duration of action exceeding 2 hr[2].
Selfotel (CGS 19755) inhibits convulsions elicited by maximal electroshock in rat (ED50 = 3.8 mg/kg i.p. 1 hr after administration) and in mouse (ED50 = 2.0 mg/kg i.p. 0.5 hr after administration)[2].
| | storage | Store at RT |
| | CIS-4-[PHOSPHONOMETHYL]-PIPERIDINE-2-CARBOXYLIC ACID Preparation Products And Raw materials |
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