Glemanserin

Glemanserin
Clinical data
ATC code	None;
Identifiers
	IUPAC name α-phenyl-1-(2-phenylethyl)-4-piperidine methanol;
CAS Number	132553-86-7;
PubChem CID	71781;
ChemSpider	64815;
UNII	X96LS7MC5Z;
CompTox Dashboard (EPA)	DTXSID4042624 ;
Chemical and physical data
Formula	C20H25NO
Molar mass	295.426 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES OC(c1ccccc1)C3CCN(CCc2ccccc2)CC3;
	InChI InChI=1S/C20H25NO/c22-20(18-9-5-2-6-10-18)19-12-15-21(16-13-19)14-11-17-7-3-1-4-8-17/h1-10,19-20,22H,11-16H2; Key:AXNGJCOYCMDPQG-UHFFFAOYSA-N;

Glemanserin (INN) (developmental code name MDL-11,939) is a drug which acts as a potent and selective 5-HT_2A receptor antagonist.^[1] The first truly selective 5-HT_2A ligand to be discovered, glemanserin resulted in the development of the widely used and even more potent and selective 5-HT_2A receptor antagonist volinanserin (MDL-100,907), which is a fluorinated analogue.^[2] Though it was largely superseded in scientific research by volinanserin, glemanserin was investigated clinically for the treatment of generalized anxiety disorder.^[3] However, it was ultimately found to be ineffective and was not marketed.^[3]

References

^ Dudley MW, Wiech NL, Miller FP, Carr AA, Cheng HC, Roebel LE, et al. (1988). "Pharmacological effects of MDL 11,939: A selective, centrally acting antagonist of 5-HT2 receptors". Drug Development Research. 13 (1): 29–43. doi:10.1002/ddr.430130104. S2CID 85075328.
^ van Wijngaarden I, Soudijn W (10 July 1997). "5-HT_2A, 5-HT_2B, and 5-HT_2C Receptor Ligands". In Olivier B (ed.). Serotonin Receptors and Their Ligands. Elsevier. p. 167. ISBN 978-0-444-82041-9. Retrieved 6 May 2012.
^ ^a ^b Sramek JJ, Robinson RE, Suri A, Cutler NR (February 1995). "Efficacy trial of the 5-HT2 antagonist MDL 11,939 in patients with generalized anxiety disorder". Journal of Clinical Psychopharmacology. 15 (1): 20–22. doi:10.1097/00004714-199502000-00004. PMID 7714223.

This drug article relating to the nervous system is a stub. You can help Wikipedia by expanding it.

[Dudley1988-1] Dudley MW, Wiech NL, Miller FP, Carr AA, Cheng HC, Roebel LE, et al. (1988). "Pharmacological effects of MDL 11,939: A selective, centrally acting antagonist of 5-HT2 receptors". Drug Development Research. 13 (1): 29–43. doi:10.1002/ddr.430130104. S2CID 85075328.

[Olivier1997-2] van Wijngaarden I, Soudijn W (10 July 1997). "5-HT_2A, 5-HT_2B, and 5-HT_2C Receptor Ligands". In Olivier B (ed.). Serotonin Receptors and Their Ligands. Elsevier. p. 167. ISBN 978-0-444-82041-9. Retrieved 6 May 2012.

[pmid7714223-3] Sramek JJ, Robinson RE, Suri A, Cutler NR (February 1995). "Efficacy trial of the 5-HT2 antagonist MDL 11,939 in patients with generalized anxiety disorder". Journal of Clinical Psychopharmacology. 15 (1): 20–22. doi:10.1097/00004714-199502000-00004. PMID 7714223.

[1]

[2]

[3]

Clinical data

ATC code	None
Identifiers
IUPAC name α-phenyl-1-(2-phenylethyl)-4-piperidine methanol
CAS Number	132553-86-7
PubChem CID	71781
ChemSpider	64815
UNII	X96LS7MC5Z
CompTox Dashboard (EPA)	DTXSID4042624
Chemical and physical data
Formula	C₂₀H₂₅NO
Molar mass	295.426 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES OC(c1ccccc1)C3CCN(CCc2ccccc2)CC3
InChI InChI=1S/C20H25NO/c22-20(18-9-5-2-6-10-18)19-12-15-21(16-13-19)14-11-17-7-3-1-4-8-17/h1-10,19-20,22H,11-16H2 Key:AXNGJCOYCMDPQG-UHFFFAOYSA-N

Glemanserin

See also

References

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