(2R,3S)-Chlorpheg is a weak antagonist of L-homocysteic acid (L-HCA) and acts on NMDA receptors. It exhibits inhibitory effects on L-HCA-induced depolarization, making it useful for studying excitatory neurotransmission. Additionally, its role as an NMDA antagonist provides insights into the modulation of synaptic plasticity and various neurological conditions. This compound is valuable for researchers investigating glutamate receptor signaling and related pathways.
(2R,3S)-Chlorpheg is a weak antagonist of L-homocysteic acid (L-HCA) and acts on NMDA receptors. It exhibits inhibitory effects on L-HCA-induced depolarization, making it useful for studying excitatory neurotransmission. Additionally, its role as an NMDA antagonist provides insights into the modulation of synaptic plasticity and various neurological conditions. This compound is valuable for researchers investigating glutamate receptor signaling and related pathways.
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