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| ATC_suffix=
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| PubChem= 132787
| PubChem= 132787
| DrugBank=
| C=21 | H=24 | N=2 | O=2
| C=21 | H=24 | N=2 | O=2
| molecular_weight = 336.427 g/mol
| molecular_weight = 336.427 g/mol
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'''S-15535''' is a [[piperazine]] [[drug]] and research chemical used in scientific studies. It is a [[Potency_(pharmacology)|potent]] and highly selective [[5-HT1A|5-HT<sub>1A</sub>]] [[receptor (biochemistry)|receptor]] [[Ligand_(biochemistry)|ligand]] which acts as an [[agonist]] and [[Antagonist (pharmacology)|antagonist]] (weak [[partial agonist]]) at the presynaptic and postsynaptic 5-HT<sub>1A</sub> receptors, respectively.<ref name="pmid8381359">{{cite journal | author = Millan MJ, Rivet JM, Canton H, Lejeune F, Gobert A, Widdowson P, Bervoets K, Brocco M, Peglion JL. | title = S 15535: a highly selective benzodioxopiperazine 5-HT1A receptor ligand which acts as an agonist and an antagonist (weak partial agonist) at presynaptic and postsynaptic sites respectively. | journal = Eur J Pharmacol. | volume = 230 | issue = 1 | pages = 99–102 | year = 1993 | pmid = 8381359 }}</ref><ref name="pmid8301575">{{cite journal | author = Millan MJ, Canton H, Gobert A, Lejeune F, Rivet JM, Bervoets K, Brocco M, Widdowson P, Mennini T, Audinot V, et al. | title = Novel benzodioxopiperazines acting as antagonists at postsynaptic 5-HT1A receptors and as agonists at 5-HT1A autoreceptors: a comparative pharmacological characterization with proposed 5-HT1A antagonists. | journal = J Pharmacol Exp Ther. | volume = 268 | issue = 1 | pages = 337–352 | year = 1994 | pmid = 8301575 }}</ref><ref name="pmid9223549">{{cite journal | author = Millan MJ, Newman-Tancredi A, Rivet JM, Brocco M, Lacroix P, Audinot V, Cistarelli L, Gobert A. | title = S 15535, a novel benzodioxopiperazine ligand of serotonin (5-HT)1A receptors: I. Interaction with cloned human (h)5-HT1A, dopamine hD2/hD3 and h alpha2A-adrenergic receptors in relation to modulation of cortical monoamine release and activity in models of potential antidepressant activity. | journal = J Pharmacol Exp Ther. | volume = 282 | issue = 1 | pages = 132–147 | year = 1997 | pmid = 9223549 }}</ref><ref name="pmid9723787">{{cite journal | author = Lejeune F, Millan MJ. | title = Induction of burst firing in ventral tegmental area dopaminergic neurons by activation of serotonin (5-HT)1A receptors: WAY 100,635-reversible actions of the highly selective ligands, flesinoxan and S 15535. | journal = Synapse. | volume = 30 | issue = 2 | pages = 172–180 | year = 1998 | pmid = 9723787 }}</ref> It has putative [[anxiolytic]] and [[antidepressant]] properties.<ref name="pmid9723787">{{cite journal | author = Lejeune F, Millan MJ. | title = Induction of burst firing in ventral tegmental area dopaminergic neurons by activation of serotonin (5-HT)1A receptors: WAY 100,635-reversible actions of the highly selective ligands, flesinoxan and S 15535. | journal = Synapse. | volume = 30 | issue = 2 | pages = 172–180 | year = 1998 | pmid = 9723787 }}</ref><ref name="pmid11041316">{{cite journal | author = Dekeyne A, Brocco M, Adhumeau A, Gobert A, Millan MJ. | title = The selective serotonin (5-HT)1A receptor ligand, S15535, displays anxiolytic-like effects in the social interaction and Vogel models and suppresses dialysate levels of 5-HT in the dorsal hippocampus of freely-moving rats. A comparison with other anxiolytic agents. | journal = Psychopharmacology (Berl). | volume = 152 | issue = 1 | pages = 55–66 | year = 2000 | pmid = 11041316 }}</ref>
'''S-15535''' is a [[piperazine]] [[drug]] and research chemical used in scientific studies. It is a [[Potency_(pharmacology)|potent]] and highly selective [[5-HT1A|5-HT<sub>1A</sub>]] [[receptor (biochemistry)|receptor]] [[Ligand_(biochemistry)|ligand]] which acts as an [[agonist]] and [[Antagonist (pharmacology)|antagonist]] (weak [[partial agonist]]) at the presynaptic and postsynaptic 5-HT<sub>1A</sub> receptors, respectively.<ref name="pmid8381359">{{cite journal | author = Millan MJ, Rivet JM, Canton H, Lejeune F, Gobert A, Widdowson P, Bervoets K, Brocco M, Peglion JL. | title = S 15535: a highly selective benzodioxopiperazine 5-HT1A receptor ligand which acts as an agonist and an antagonist (weak partial agonist) at presynaptic and postsynaptic sites respectively. | journal = Eur J Pharmacol. | volume = 230 | issue = 1 | pages = 99–102 | year = 1993 | pmid = 8381359 }}</ref><ref name="pmid8301575">{{cite journal | author = Millan MJ, Canton H, Gobert A, Lejeune F, Rivet JM, Bervoets K, Brocco M, Widdowson P, Mennini T, Audinot V, et al. | title = Novel benzodioxopiperazines acting as antagonists at postsynaptic 5-HT1A receptors and as agonists at 5-HT1A autoreceptors: a comparative pharmacological characterization with proposed 5-HT1A antagonists. | journal = J Pharmacol Exp Ther. | volume = 268 | issue = 1 | pages = 337–352 | year = 1994 | pmid = 8301575 }}</ref><ref name="pmid9223549">{{cite journal | author = Millan MJ, Newman-Tancredi A, Rivet JM, Brocco M, Lacroix P, Audinot V, Cistarelli L, Gobert A. | title = S 15535, a novel benzodioxopiperazine ligand of serotonin (5-HT)1A receptors: I. Interaction with cloned human (h)5-HT1A, dopamine hD2/hD3 and h alpha2A-adrenergic receptors in relation to modulation of cortical monoamine release and activity in models of potential antidepressant activity. | journal = J Pharmacol Exp Ther. | volume = 282 | issue = 1 | pages = 132–147 | year = 1997 | pmid = 9223549 }}</ref><ref name="pmid9723787">{{cite journal | author = Lejeune F, Millan MJ. | title = Induction of burst firing in ventral tegmental area dopaminergic neurons by activation of serotonin (5-HT)1A receptors: WAY 100,635-reversible actions of the highly selective ligands, flesinoxan and S 15535. | journal = Synapse. | volume = 30 | issue = 2 | pages = 172–180 | year = 1998 | pmid = 9723787 }}</ref> It has [[anxiolytic]] properties.<ref name="pmid9723787">{{cite journal | author = Lejeune F, Millan MJ. | title = Induction of burst firing in ventral tegmental area dopaminergic neurons by activation of serotonin (5-HT)1A receptors: WAY 100,635-reversible actions of the highly selective ligands, flesinoxan and S 15535. | journal = Synapse. | volume = 30 | issue = 2 | pages = 172–180 | year = 1998 | pmid = 9723787 }}</ref><ref name="pmid11041316">{{cite journal | author = Dekeyne A, Brocco M, Adhumeau A, Gobert A, Millan MJ. | title = The selective serotonin (5-HT)1A receptor ligand, S15535, displays anxiolytic-like effects in the social interaction and Vogel models and suppresses dialysate levels of 5-HT in the dorsal hippocampus of freely-moving rats. A comparison with other anxiolytic agents. | journal = Psychopharmacology (Berl). | volume = 152 | issue = 1 | pages = 55–66 | year = 2000 | pmid = 11041316 }}</ref>

{{pharm-stub}}


== References ==
== References ==
{{reflist}}
{{Reflist|2}}



{{Anxiolytics}}
{{Serotonergics}}
{{Serotonergics}}
{{Piperazines}}
{{Piperazines}}
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[[Category:Piperazines]]
[[Category:Piperazines]]
[[Category:Indanes]]
[[Category:Indanes]]


{{pharmacology-stub}}

Revision as of 12:47, 16 January 2010

S-15535
Identifiers
  • 1-(2,3-dihydro-1,4-benzodioxin-8-yl)-4-(2,3-dihydro-1H-inden-2-yl)piperazine
CAS Number
PubChem CID
CompTox Dashboard (EPA)
ECHA InfoCard100.150.279 Edit this at Wikidata
Chemical and physical data
FormulaC21H24N2O2
Molar mass336.427 g/mol g·mol−1
3D model (JSmol)
  • C1CN(CCN1C2CC3=CC=CC=C3C2)C4=C5C(=CC=C4)OCCO5

S-15535 is a piperazine drug and research chemical used in scientific studies. It is a potent and highly selective 5-HT1A receptor ligand which acts as an agonist and antagonist (weak partial agonist) at the presynaptic and postsynaptic 5-HT1A receptors, respectively.[1][2][3][4] It has anxiolytic properties.[4][5]

References

  1. ^ Millan MJ, Rivet JM, Canton H, Lejeune F, Gobert A, Widdowson P, Bervoets K, Brocco M, Peglion JL. (1993). "S 15535: a highly selective benzodioxopiperazine 5-HT1A receptor ligand which acts as an agonist and an antagonist (weak partial agonist) at presynaptic and postsynaptic sites respectively". Eur J Pharmacol. 230 (1): 99–102. PMID 8381359.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. ^ Millan MJ, Canton H, Gobert A, Lejeune F, Rivet JM, Bervoets K, Brocco M, Widdowson P, Mennini T, Audinot V; et al. (1994). "Novel benzodioxopiperazines acting as antagonists at postsynaptic 5-HT1A receptors and as agonists at 5-HT1A autoreceptors: a comparative pharmacological characterization with proposed 5-HT1A antagonists". J Pharmacol Exp Ther. 268 (1): 337–352. PMID 8301575. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  3. ^ Millan MJ, Newman-Tancredi A, Rivet JM, Brocco M, Lacroix P, Audinot V, Cistarelli L, Gobert A. (1997). "S 15535, a novel benzodioxopiperazine ligand of serotonin (5-HT)1A receptors: I. Interaction with cloned human (h)5-HT1A, dopamine hD2/hD3 and h alpha2A-adrenergic receptors in relation to modulation of cortical monoamine release and activity in models of potential antidepressant activity". J Pharmacol Exp Ther. 282 (1): 132–147. PMID 9223549.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^ a b Lejeune F, Millan MJ. (1998). "Induction of burst firing in ventral tegmental area dopaminergic neurons by activation of serotonin (5-HT)1A receptors: WAY 100,635-reversible actions of the highly selective ligands, flesinoxan and S 15535". Synapse. 30 (2): 172–180. PMID 9723787.
  5. ^ Dekeyne A, Brocco M, Adhumeau A, Gobert A, Millan MJ. (2000). "The selective serotonin (5-HT)1A receptor ligand, S15535, displays anxiolytic-like effects in the social interaction and Vogel models and suppresses dialysate levels of 5-HT in the dorsal hippocampus of freely-moving rats. A comparison with other anxiolytic agents". Psychopharmacology (Berl). 152 (1): 55–66. PMID 11041316.{{cite journal}}: CS1 maint: multiple names: authors list (link)