5-HT Receptor Antagonists 5-HT Receptor agonists AChR antagonist Adrenergic Receptor agonists COX inhibitors Histamine Receptor Antagonists AChR agonist 5-HT Receptor modulators GluR agonist GluR antagonist 5-HT Receptor Inhibitor Adrenergic Receptor Antagonists Dopamine Receptor agonists Dopamine Receptor Antagonists Adrenergic Receptor Inhibitors AChR inhibitor Histamine Receptor Inhibitors Histamine Receptor agonists GABA Receptor agonists Opioid Receptor Antagonists CaMK inhibitors P2 Receptor Inhibitors P2 Receptor Antagonists AMPA and kainate receptors Beta Amyloid Inhibitors BACE inhibitors AChR modifiers Opioid Receptor agonists GluR modifiers GluR inhibitors
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Neuronal Signaling

5-HT Receptor Antagonists 5-HT Receptor agonists AChR antagonist Adrenergic Receptor agonists COX inhibitors Histamine Receptor Antagonists AChR agonist 5-HT Receptor modulators GluR agonist GluR antagonist 5-HT Receptor Inhibitor Adrenergic Receptor Antagonists Dopamine Receptor agonists Dopamine Receptor Antagonists Adrenergic Receptor Inhibitors AChR inhibitor Histamine Receptor Inhibitors Histamine Receptor agonists GABA Receptor agonists Opioid Receptor Antagonists CaMK inhibitors P2 Receptor Inhibitors P2 Receptor Antagonists AMPA and kainate receptors Beta Amyloid Inhibitors BACE inhibitors AChR modifiers Opioid Receptor agonists GluR modifiers GluR inhibitors
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The neural signals directly characterize the meaning of the human self. Studying the neural signal provides an approach for understanding and identifying the human body. Nerve signals share some similar features with other human biological signals, but also have some of its unique features. According to the research in neurobiology, nerve signal, resembling a pulse electric signal, has a frequency of generally around 1 kHz and can be as high as 10 kHz. For example, for a bundle of movement nerves that control muscle, when there is potential impulse signal arriving, the muscle fiber will have contractile response. The contraction strength, depending on the difference of the impulse frequency of nerve, will have the strength difference.

Learning and memory is an important area of research, not only because they dominate the normal human behavior, but also because it plays an important role in the development of nervous system diseases and disorders, which includes addiction, anxiety, depression, schizophrenia and neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease. At present, we haven’t achieved any significant efficacy for treatment aim to alleviate the learning and memory dysfunction. Therefore, pharmaceutical companies are quite interested in drug target which can improve the cognitive function including specific serotonin or serotonin receptors. What the serotonin system dominated are the specific brain regions which play an important regulatory role in the memory and learning processes.

This kind of neural domination is related the expression of a series of serotonin receptors (the drug target of serotonin). An important feature of the serotonin system is the universality of the neural domination of forebrain, which is originated from the discrete cluster located in raphe nuclei and the diversity of its receptors. The number of its receptors is up to 14, including 5-HT1A, 5 -HT4 and 5-HT6, and these receptors are all densely presented in the brain regions associated with learning and memory, and have impact on human cognitive impairment. Furthermore, selective agonist and/or antagonist compounds may take effect through acting on the three postsynaptic receptors to affect the clinical behavior patterns. These compounds, upon binding to the receptor, may also modulate neurotransmitter system instead of altering the release of 5-HT, thereby affecting the learning and memory.
GluR related chemicals are very popular. Ampakines, one kind of pyrrolidone derivatives, can act on α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptor with its upregulation may enhance the synaptic plasticity. Early results of clinical studies have indicated ampakines may have a role in schizophrenia. Similarly, D-serine and D-cycloserine can stimulate the glycine co-agonist site located in the NMDA receptor which is insensitive to strychnine on, but also can enhance NMDA receptor activity. Such agents can improve the conditioned reflex of the clinical fear, and may also moderately improve the negative reactions and cognitive dysfunction in schizophrenia. Dopamine receptor is a hot filed in neurology and psychiatry. Receptors (D1, D2, D3, D4 and D5) are related the physiological functions of catecholamine neurotransmitter dopamine. Dopaminergic neurotransmission have been used to study Parkinson's disease, schizophrenia, bipolar disorder, Huntington's disease, attention deficit hyperactivity disorder and Tourette syndrome.The target of the neurological and psychiatric studies also include H3 receptor antagonists, COX receptors, γ- secretion, Glu receptor, adrenergic receptor, acetylcholine receptor, P-gp, P2 receptors and opioid receptors.

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