WAY-100,635
200px | |
Systematic (IUPAC) name | |
---|---|
N-[2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]- N-(2-pyridyl)cyclohexanecarboxamide | |
Identifiers | |
CAS Number | 146714-97-8 |
PubChem | CID 5684 |
IUPHAR/BPS | 80 |
Chemical data | |
Formula | C25H34N4O2 |
Molar mass | 422.56 g/mol[[Script error: No such module "String".]] |
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WAY-100,635 is a piperazine drug and research chemical widely used in scientific studies. It was originally believed to act as a selective 5-HT1A receptor antagonist, but subsequent research showed that it also acts as potent full agonist at the D4 receptor.[1][2][3] It is sometimes referred to as a silent antagonist at the former receptor.[4] It is closely related to WAY-100,135.
In light of its only recently discovered dopaminergic activity, conclusions drawn from studies that employed WAY-100635 as a selective 5-HT1A antagonist may need to be re-evaluated.
Human PET studies
In human PET studies WAY-100,635 shows high binding in the cerebral cortex, hippocampus, raphe nucleus and amygdaloid nucleus, while lower in thalamus and basal ganglia.[5] One study described a case with relatively high binding in the cerebellum.[6]
In relating its binding to subject variables one Swedish study found WAY-100,635 binding in raphe brain region correlating with self-transcendence and spiritual acceptance personality traits.[7] WAY-100,635 binding has also been assessed in connection with clinical depression, where there has been disagreement about the presence and direction of the 5-HT1A receptor binding.[8] In healthy subjects WAY-100,635 binding has been found to decline with age,[9] — though not all studies have found this relationship.[10][11]
What | Result | Subjects | Ref. |
---|---|---|---|
Age | Global decrease and particularly in parietal cortex and dorsolateral prefrontal cortex | 19 | [9] |
Age | No correlation found | 61 | [10] |
Age | No correlation detected | 25 | [11] |
Sex | Higher binding in females | 25 | [11] |
TCI self-transcendence and spiritual acceptance personality traits | Positive correlation in raphe region | 15 males | [7] |
Lifetime aggression | Negative correlation | 25 | [11] |
MADAM binding potential (serotonin transporter binding) | Positive correlation in the raphe nuclei and hippocampus | 12 males | [12] |
Genetic variation | Result | Subjects | Ref. |
HTR1A.(-1018)C>G polymorphism | No difference found | 35 | [13] |
SERT.5-HTTLPR polymorphism | Lower binding in "all brain regions" for SS or SL genotypes compared to LL | 35 | [13] |
Disease | Result | Subjects | Ref. |
Depressive (with primary, recurrent, familial mood disorders) | Reduction in raphe nucleus and mesiotemporal cortex | 12+8 | [14] |
Major depressive disorder (medicated and unmedicated) | Reduction in "many of the regions examined" | 25+18 | [15] |
Panic disorder in treated and untreated patients | Reducing in binding in raphe in both treated and untreated. Reduced binding in global postsynaptic regions for untreated, while no or little reduction for treated. | 9+7+19 | [16] |
Alzheimer disease | Decrease in right medial temporal cortex | 10+10 | [17] |
Radioligands
Labeled with the radioisotope carbon-11 it is used as a radioligand in positron emission tomography (PET) studies to determine neuroreceptor binding in the brain.[18] WAY-100,635 may be labeled in different ways with carbon-11: As [carbonyl-11C]WAY-100,635 or [O-methyl-11C]WAY-100,635, with [carbonyl-11C]WAY-100635 regarded as "far superior".[19] Labeled with tritium WAY-100,635 may also be used in autoradiography.[20] WAY-100,635 has higher 5-HT1A affinity than 8-OH-DPAT.[21]
See also
- Binding potential
- Other radioligands for the serotonin system:
External links
- Vesa Oikonen (2007). "Quantification of (carbonyl-11C)WAY-100635 PET studies". Turku PET center.
References
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- ↑ C. A. Fornal, C. W. Metzler, R. A. Gallegos, S. C. Veasey, A. C. McCreary and B. L. Jacobs (1996). "WAY-100635, a potent and selective 5-hydroxytryptamine1A antagonist, increases serotonergic neuronal activity in behaving cats: comparison with (S)-WAY-100135". The Journal of Pharmacology and Experimental Therapeutics. 278 (2): 752–762. PMID 8768728.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ Marona-Lewicka D, Nichols DE (2009). "WAY 100635 produces discriminative stimulus effects in rats mediated by dopamine D(4) receptor activation". Behav Pharmacol. 20 (1): 114–8. doi:10.1097/FBP.0b013e3283242f1a. PMID 19179855.
- ↑ A. Fletcher, E. A. Forster, D. J. Bill, G. Brown, I. A. Cliffe, J. E. Hartley, D. E. Jones, A. McLenachan, K. J. Stanhope, D. J. Critchley, K. J. Childs, V. C. Middlefell, L. Lanfumey, R. Corradetti, A. M. Laporte, H. Gozlan, M. Hamon & C. T. Dourish (1996). "Electrophysiological, biochemical, neurohormonal and behavioural studies with WAY-100635, a potent, selective and silent 5-HT1A receptor antagonist". Behavioural Brain Research. 73 (1-2): 337–333. doi:10.1016/0166-4328(96)00118-0. PMID 8788530.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
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- ↑ Jon R. Nash, Peter A. Sargent, Eugenii A. Rabiner, Sean D. Hood, Paul M. Grasby & David J. Nutt (2008). "Serotonin 5-HT1A receptor binding in people with panic disorder: positron emission tomography study". The British Journal of Psychiatry. 193: 229–234. doi:10.1192/bjp.bp.107.041186.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
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