Binospirone

Anxiolytic drug
  • none
Identifiers
  • 8-[2-(2,3-dihydro-1,4-benzodioxin-2-ylmethylamino)ethyl]-8-azaspiro[4.5]decane-7,9-dione
CAS Number
  • 102908-59-8 checkY
  • mesylate: 124756-23-6 checkY
PubChem CID
  • 60769
ChemSpider
  • 54766
UNII
  • T3M5D109V5
  • mesylate: 155R3B9K8H checkY
ChEMBL
  • ChEMBL1487115
Chemical and physical dataFormulaC20H26N2O4Molar mass358.438 g·mol−13D model (JSmol)
  • Interactive image
  • O=C1N(C(=O)CC2(C1)CCCC2)CCNCC3Oc4ccccc4OC3
InChI
  • InChI=1S/C20H26N2O4/c23-18-11-20(7-3-4-8-20)12-19(24)22(18)10-9-21-13-15-14-25-16-5-1-2-6-17(16)26-15/h1-2,5-6,15,21H,3-4,7-14H2
  • Key:BVMYCHKQPGEOSI-UHFFFAOYSA-N
  (verify)

Binospirone (MDL-73,005-EF) is a drug which acts as a partial agonist at 5-HT1A somatodendritic autoreceptors but as an antagonist at postsynaptic 5-HT1A receptors.[1] It has anxiolytic effects.[2]

See also

  • Azapirone

References

  1. ^ Bertrand F, Lehmann O, Galani R, Lazarus C, Jeltsch H, Cassel JC (April 2001). "Effects of MDL 73005 on water-maze performances and locomotor activity in scopolamine-treated rats". Pharmacology, Biochemistry, and Behavior. 68 (4): 647–60. doi:10.1016/S0091-3057(01)00448-8. PMID 11526961. S2CID 8595441.
  2. ^ Moser PC, Tricklebank MD, Middlemiss DN, Mir AK, Hibert MF, Fozard JR (February 1990). "Characterization of MDL 73005EF as a 5-HT1A selective ligand and its effects in animal models of anxiety: comparison with buspirone, 8-OH-DPAT and diazepam". British Journal of Pharmacology. 99 (2): 343–9. doi:10.1111/j.1476-5381.1990.tb14706.x. PMC 1917389. PMID 1970269.
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Anxiolytics (N05B)
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  • See also: Receptor/signaling modulators
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Simple piperazines
(no additional rings)
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