Levosulpiride

Clinical data
ATC code	N05AL07 (WHO)
Identifiers
IUPAC name N-(2S)-1-ethylpyrrolidin-2-ylmethyl-2-methoxy-5-sulfamoylbenzamide
CAS Number	23672-07-3
PubChem CID	688272
IUPHAR/BPS	958
DrugBank	DB00391
ChemSpider	599749
UNII	JTG7R315LK
KEGG	D07312
ChEBI	CHEBI:64119
ChEMBL	ChEMBL267044
CompTox Dashboard (EPA)	DTXSID0042583
Chemical and physical data
Formula	C15H23N3O4S
Molar mass	341.43 g·mol−1
3D model (JSmol)	Interactive image
SMILES CCN1CCCC@H1CNC(=O)C2=C(C=CC(=C2)S(=O)(=O)N)OC
InChI InChI=1S/C15H23N3O4S/c1-3-18-8-4-5-11(18)10-17-15(19)13-9-12(23(16,20)21)6-7-14(13)22-2/h6-7,9,11H,3-5,8,10H2,1-2H3,(H,17,19)(H2,16,20,21)/t11-/m0/s1 Key:BGRJTUBHPOOWDU-NSHDSACASA-N
NY (what is this?)  (verify)

Levosulpiride, sold under the brand name SULPEPTA , is a potent prokinetic agent of the benzamide class.^[1] It is a selective antagonist of the dopamine D₂ receptors and 5HT4 Agonism ^[2] on both central and peripheral nervous systems. Levosulpiride is claimed to have mood elevating properties.

Chemically, it is the (S)-(−)-enantiomer of sulpiride.

Usesedit

Levosulpiride is used in the treatment of:

• Psychosis
• Negative symptoms of schizophrenia
• Anxiety disorders
• Dysthymia
• Vertigo
• Dyspepsia
• Irritable bowel syndrome
• Premature ejaculation.

Levosulpiride is not currently licensed for treatment of premature ejaculation in the UK or other European countries.^[3]

Side effectsedit

Side effects include amenorrhea, gynecomastia, galactorrhea, changes in libido, and neuroleptic malignant syndrome.^[4] In the U.S., as of 2013 only one case of adverse reaction to levosulpiride had been recorded on the FDA Adverse Event Reporting System Database.^[3] A case of rapid onset resistant dystonia caused by low dose levosulpiride was reported in India.^[5]

Mechanism of actionedit

In contrast to most other neuroleptics which block both D₁ and D₂ receptors, levosulpiride is more selective and acts primarily as a D₂ antagonist. Levosulpiride appears to lack effects on norepinephrine, acetylcholine, serotonin, histamine, and gamma-aminobutyric acid (GABA) receptors.^[6]

Pharmacodynamicsedit

Levosulpiride is a substituted benzamide derivative and a selective dopamine D₂ antagonist with antipsychotic and antidepressant activity. Other benzamide derivatives include metoclopramide, tiapride, and sultopride.^[6]

See alsoedit

• Sulpiride
• Veralipride
• Benzamide

Referencesedit