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词条 CBiPES
释义

  1. References

{{Drugbox
| IUPAC_name = N-(4'-cyano-[1,1'-biphenyl]-3-yl-N-(3-pyridinylmethyl)ethanesulfonamide
| image = CBiPES_structure.png
| width = 200
| tradename =
| pregnancy_AU =
| pregnancy_US =
| pregnancy_category =
| legal_AU =
| legal_CA =
| legal_UK =
| legal_US =
| legal_status =
| routes_of_administration =
| bioavailability =
| protein_bound =
| metabolism =
| elimination_half-life =
| excretion =
| IUPHAR_ligand = 3372
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 856702-40-4
| ATC_prefix = none
| ATC_suffix =
| PubChem = 9864510
| DrugBank =
| ChemSpiderID = 8040202
| StdInChI = 1S/C21H19N3O2S/c1-2-27(25,26)24(16-18-5-4-12-23-15-18)21-7-3-6-20(13-21)19-10-8-17(14-22)9-11-19/h3-13,15H,2,16H2,1H3
| StdInChIKey = HDVYXILCBYGKGU-UHFFFAOYSA-N
| C=21 | H=19 | N=3 | O=2 | S=1
| molecular_weight = 377.459 g/mol
| smiles = N#Cc1ccc(cc1)-c(ccc2)cc2N(S(=O)(=O)CC)Cc3cccnc3
}}CBiPES is a drug used in scientific research that acts as a selective positive allosteric modulator for the metabotropic glutamate receptor group II subtype mGluR2. It has potentially antipsychotic effects in animal models, and is used for researching the role of mGluR2 receptors in schizophrenia and related disorders.[1][2][3]

References

1. ^{{Cite journal | last1 = Johnson | first1 = M. P. | last2 = Barda | first2 = D. | last3 = Britton | first3 = T. C. | last4 = Emkey | first4 = R. | last5 = Hornback | first5 = W. J. | last6 = Jagdmann | first6 = G. E. | last7 = McKinzie | first7 = D. L. | last8 = Nisenbaum | first8 = E. S. | last9 = Tizzano | first9 = J. P. | doi = 10.1007/s00213-004-2099-9 | last10 = Schoepp | first10 = D. D. | title = Metabotropic glutamate 2 receptor potentiators: Receptor modulation, frequency-dependent synaptic activity, and efficacy in preclinical anxiety and psychosis model(s) | journal = Psychopharmacology | volume = 179 | issue = 1 | pages = 271–283 | year = 2005 | pmid = 15717213 | pmc = }}
2. ^{{Cite journal | last1 = Fell | first1 = M. J. | last2 = Katner | first2 = J. S. | last3 = Johnson | first3 = B. G. | last4 = Khilevich | first4 = A. | last5 = Schkeryantz | first5 = J. M. | last6 = Perry | first6 = K. W. | last7 = Svensson | first7 = K. A. | doi = 10.1016/j.neuropharm.2009.11.014 | title = Activation of metabotropic glutamate (mGlu)2 receptors suppresses histamine release in limbic brain regions following acute ketamine challenge | journal = Neuropharmacology | volume = 58 | issue = 3 | pages = 632–639 | year = 2010 | pmid = 19951716 | pmc = }}
3. ^{{Cite journal | last1 = Sanger | first1 = H. | last2 = Hanna | first2 = L. | last3 = Colvin | first3 = E. M. | last4 = Grubisha | first4 = O. | last5 = Ursu | first5 = D. | last6 = Heinz | first6 = B. A. | last7 = Findlay | first7 = J. D. | last8 = Vivier | first8 = R. G. | last9 = Sher | first9 = E. | last10 = Lodge | first10 = D. | last11 = Monn | first11 = J. A. | last12 = Broad | first12 = L. M. | title = Pharmacological profiling of native group II metabotropic glutamate receptors in primary cortical neuronal cultures using a FLIPR | doi = 10.1016/j.neuropharm.2012.05.023 | journal = Neuropharmacology | volume = 66 | pages = 264–273 | year = 2012 | pmid = 22659090 | pmc = }}
{{Metabotropic glutamate receptor modulators}}{{nervous-system-drug-stub}}

3 : Antipsychotics|MGlu2 receptor agonists|MGlu3 receptor agonists

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