TC-1698: Difference between revisions
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{{Short description|Chemical compound}} |
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{{Drugbox |
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| image=TC-1698_structure.png |
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| image = TC-1698.svg |
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| ATC_prefix= |
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<!--Clinical data--> |
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| tradename = |
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<!--Identifiers--> |
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| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} |
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| ChemSpiderID = 8305933 |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| ChEMBL_Ref = {{ebicite|changed|EBI}} |
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| DrugBank= |
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| ChEMBL = 2151442 |
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| molecular_weight = 202.295 |
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<!--Chemical data--> |
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| C=13 | H=18 | N=2 |
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| smiles = c2ncccc2C1CCC3CCN1CC3 |
| smiles = c2ncccc2C1CCC3CCN1CC3 |
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| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
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| bioavailability= |
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| StdInChI = 1S/C13H18N2/c1-2-12(10-14-7-1)13-4-3-11-5-8-15(13)9-6-11/h1-2,7,10-11,13H,3-6,8-9H2 |
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| metabolism = |
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| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
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| elimination_half-life= |
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| StdInChIKey = WIEWCOLOPGXZDJ-UHFFFAOYSA-N |
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'''TC-1698''' is a drug developed by [[Targacept]] which acts as a [[partial agonist]] for the [[Alpha-7 nicotinic receptor|α7]] subtype of neural [[nicotinic acetylcholine receptor]]s.<ref>{{ |
'''TC-1698''' is a drug developed by [[Targacept]] which acts as a [[partial agonist]] for the [[Alpha-7 nicotinic receptor|α7]] subtype of neural [[nicotinic acetylcholine receptor]]s.<ref>{{cite journal | vauthors = Romanelli MN, Gratteri P, Guandalini L, Martini E, Bonaccini C, Gualtieri F | title = Central nicotinic receptors: structure, function, ligands, and therapeutic potential | journal = ChemMedChem | volume = 2 | issue = 6 | pages = 746–67 | date = June 2007 | pmid = 17295372 | doi = 10.1002/cmdc.200600207 | s2cid = 34763474 }}</ref> It has [[neuroprotective]] effects in animal studies,<ref>{{cite journal | vauthors = Marrero MB, Papke RL, Bhatti BS, Shaw S, Bencherif M | title = The neuroprotective effect of 2-(3-pyridyl)-1-azabicyclo[3.2.2]nonane (TC-1698), a novel alpha7 ligand, is prevented through angiotensin II activation of a tyrosine phosphatase | journal = The Journal of Pharmacology and Experimental Therapeutics | volume = 309 | issue = 1 | pages = 16–27 | date = April 2004 | pmid = 14722323 | doi = 10.1124/jpet.103.061655 | s2cid = 7730290 | citeseerx = 10.1.1.420.2457 }}</ref> and has been used as a [[lead compound]] to find further potent derivatives.<ref>{{cite journal | vauthors = Bhatti BS, Strachan JP, Breining SR, Miller CH, Tahiri P, Crooks PA, Deo N, Day CS, Caldwell WS | display-authors = 6 | title = Synthesis of 2-(pyridin-3-yl)-1-azabicyclo[3.2.2]nonane, 2-(pyridin-3-yl)-1-azabicyclo[2.2.2]octane, and 2-(pyridin-3-yl)-1-azabicyclo[3.2.1]octane, a class of potent nicotinic acetylcholine receptor-ligands | journal = The Journal of Organic Chemistry | volume = 73 | issue = 9 | pages = 3497–507 | date = May 2008 | pmid = 18363376 | doi = 10.1021/jo800028q }}</ref> |
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==See also== |
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* [[Anabasine]] |
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== References == |
== References == |
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{{Reflist|2}} |
{{Reflist|2}} |
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{{Stimulants}} |
{{Stimulants}} |
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{{Nootropics}} |
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{{Cholinergics}} |
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{{Nicotinic acetylcholine receptor modulators}} |
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[[Category:Nicotinic agonists]] |
[[Category:Nicotinic agonists]] |
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[[Category:Stimulants]] |
[[Category:Stimulants]] |
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[[Category: |
[[Category:3-Pyridyl compounds]] |
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