CIS-4-[PHOSPHONOMETHYL]-PIPERIDINE-2-CARBOXYLIC ACID
CIS-4-[PHOSPHONOMETHYL]-PIPERIDINE-2-CARBOXYLIC ACID Basic information
- Product Name:
- CIS-4-[PHOSPHONOMETHYL]-PIPERIDINE-2-CARBOXYLIC ACID
- Synonyms:
-
- 4-(phosphonomethyl)-2-piperidinecarboxylic acid
- CGS 19755
- CIS-4-[PHOSPHONOMETHYL]-PIPERIDINE-2-CARBOXYLIC ACID
- Selfotel
- CGS-19755 \ POTENT COMPETITIVE NMDA RECE
- cis-4-[Phosphomethyl]-piperidine-2-carboxylicacid
- LY-272541
- CPDD 0027
- CAS:
- 110347-85-8
- MF:
- C7H14NO5P
- MW:
- 223.16
- Product Categories:
-
- Glutamate receptor
- Mol File:
- 110347-85-8.mol
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
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