N-Methylspiperone

This article will address the topic of N-Methylspiperone, exploring its different facets and meanings. From its origin to its relevance today, N-Methylspiperone has been the subject of interest and debate in various spheres of society. Through a deep and detailed analysis, we will seek to shed light on the key aspects surrounding N-Methylspiperone, as well as offer an enriching vision and interesting perspectives on its impact on culture, history, politics or any other relevant field. In order to deepen the understanding of this significant topic, its practical implications and possible ramifications for the future will also be examined.

N-Methylspiperone
Names
IUPAC name
8--3-methyl-1-phenyl-1,3,8-triazaspirodecan-4-one
Other names
3-N-Methylspiperone
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C24H28FN3O2/c1-26-18-28(21-6-3-2-4-7-21)24(23(26)30)13-16-27(17-14-24)15-5-8-22(29)19-9-11-20(25)12-10-19/h2-4,6-7,9-12H,5,8,13-18H2,1H3 ☒N
    Key: QHJLPOSPWKZACG-UHFFFAOYSA-N ☒N
  • InChI=1/C24H28FN3O2/c1-26-18-28(21-6-3-2-4-7-21)24(23(26)30)13-16-27(17-14-24)15-5-8-22(29)19-9-11-20(25)12-10-19/h2-4,6-7,9-12H,5,8,13-18H2,1H3
    Key: QHJLPOSPWKZACG-UHFFFAOYAB
  • CN1CN(C2(C1=O)CCN(CC2)CCCC(=O)C3=CC=C(C=C3)F)C4=CC=CC=C4
Properties
C24H28FN3O2
Molar mass 409.505 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
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N-Methylspiperone (NMSP) is a derivate of spiperone that is used to study the dopamine and serotonin neurotransmitter systems. Labeled with the radioisotope carbon-11, it can be used for positron emission tomography.[1]

References

  1. ^ Bengt Andree; et al. (August 1998). "Positron Emission Tomographic Analysis of Dose-dependent MDL-100,907 Binding to 5-Hydroxtryptamine-2A Receptors in the Human Brain". Journal of Clinical Psychopharmacology. 18 (4): 313–323.



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