Structure via PubChem · Public domain (PubChem)
perospirone
Sign in to saveAlso known as Lullan® (Japan), SM-9018, cis-N-(4-(4-(1,2-Benzisothiazol-3-yl)-1-piperazinyl)butyl)-1,2-cyclohexanedicarboximide
Perospirone (Lullan) is an atypical antipsychotic of the azapirone family. It was introduced in Japan by Dainippon Sumitomo Pharma in 2001 for the treatment of schizophrenia and acute cases of bipolar mania.
In the Vinony graph
Within Vinony's link graph, perospirone is referenced by 1,932 other articles, and connects out to propranolol, fluphenazine and zuclopenthixol.
It sits within the topics Atypical antipsychotics, Azapirones and Chemical pages without DrugBank identifier.
Its subject is documented across 11 Wikipedia language editions.
Chemical data
- Formula
- C23H30N4O2S
- Molecular weight
- 426.6 g/mol
- IUPAC name
- (3aR,7aS)-2-[4-[4-(1,2-benzothiazol-3-yl)piperazin-1-yl]butyl]-3a,4,5,6,7,7a-hexahydroisoindole-1,3-dione
- SMILES
- C1CC[C@H]2[C@@H](C1)C(=O)N(C2=O)CCCCN3CCN(CC3)C4=NSC5=CC=CC=C54
- InChIKey
- FBVFZWUMDDXLLG-HDICACEKSA-N
- XLogP
- 3.9
- Polar surface area
- 85 Ų
- H-bond donors
- 0
- H-bond acceptors
- 6
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
176 papers- Perospirone.CNS drugs · 2001
- Perospirone (Sumitomo Pharmaceuticals).Current opinion in investigational drugs (London, England : 2000) · 2002
- [Pharmacological characteristics of perospirone hydrochloride, a novel antipsychotic agent].Nihon yakurigaku zasshi. Folia pharmacologica Japonica · 2000
- Antihyperalgesic effects of intrathecal perospirone in a rat model of neuropathic pain.Pharmacology, biochemistry, and behavior · 2020
- Efficacy and tolerability of perospirone in schizophrenia: a systematic review and meta-analysis of randomized controlled trials.CNS drugs · 2013
via PubMed
Wikidata facts
- Subclass of
- heterocyclic compound
- Mass
- 426.208947
- Has use
- medication
Show 5 more facts
- subject has role
- antipsychotics
- chemical formula
- C₂₃H₃₀N₄O₂S
- isomeric SMILES
- C1CC[C@H]2[C@@H](C1)C(=O)N(C2=O)CCCCN3CCN(CC3)C4=NSC5=CC=CC=C54
- canonical SMILES
- C1CCC2C(C1)C(=O)N(C2=O)CCCCN3CCN(CC3)C4=NSC5=CC=CC=C54
- Commons category
- Perospirone
Sources (2)
via Wikidata · CC0
~3 min read
Encyclopedic overview
7 sectionsContents
- Medical uses
- Schizophrenia
- Adverse effects
- Discontinuation
- Pharmacology
- See also
- References
Perospirone (Lullan) is an atypical antipsychotic of the azapirone family. It was introduced in Japan by Dainippon Sumitomo Pharma in 2001 for the treatment of schizophrenia and acute cases of bipolar mania.
==Medical uses== Its primary uses are in the treatment of schizophrenia and bipolar mania.
Excerpted from Wikipedia’s “perospirone” article, available under the CC BY-SA 4.0 licence.