(2R,3S)-Chlorpheg

• UNSPSC Description:

  (2R,3R)-Chlorpheg is a week antagonist of L-homocysteic acid (L-HCA) induced depolarization.(2R,3R)-Chlorpheg also is a weak N-methyl-D-aspartate (NMDA) antagonist[1].

• Target Antigen:

  iGluR

• Type:

  Reference compound

• Related Pathways:

  Membrane Transporter/Ion Channel;Neuronal Signaling

• Applications:

  Neuroscience-Neurodegeneration

• Field of Research:

  Neurological Disease

• Assay Protocol:

  https://www.medchemexpress.com/2r-3r-chlorpheg.html

• Solubility:

  10 mM in DMSO

• Smiles:

  N[C@H]([C@@H](C1=CC=C(Cl)C=C1)CC(O)=O)C(O)=O

• Molecular Weight:

  257.67

• References & Citations:

  [1]D J Chalmers, et, al. Differential actions of 3-(4-chlorophenyl) glutamic acid stereoisomers and L-trans-pyrrolidine-2,4-dicarboxylic acid upon L-homocysteic acid- and L-glutamic acid-induced responses from rat spinal motoneurones. Neuropharmacology. 1995, 34, 12.

• Shipping Conditions:

  Room temperature

• Clinical Information:

  No Development Reported

• CAS Number:

  140924-23-8