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150915-41-6

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150915-41-6 Usage

Description

Perospirone, also known as Perospirone hydrochloride, is a medication primarily used for the treatment of schizophrenia and other psychoses. It is a structurally-related analog of ziprasidone and has been launched in Japan as a new treatment option. Perospirone exhibits high affinity for 5-HT2, 5-HT1A, and D2 receptors, as well as a significant but lower affinity for DI and al receptors. Its unique binding profile and high in vivo occupancy of 5-HT2A receptors with lower D2 occupancy contribute to a significantly lower propensity for the development of extrapyramidal symptoms (EPS) and tardive schizophrenia, which are the main side effects associated with classical antipsychotic therapy. Additionally, perospirone has shown anxiolytic-like effects in animal models and has demonstrated efficacy in long-term clinical trials for treating the positive, negative, and general symptoms of schizophrenia.

Uses

Used in Pharmaceutical Industry:
Perospirone is used as an antipsychotic agent for the treatment of schizophrenia and other psychoses. Its unique binding profile and high affinity for specific neurotransmitter receptors contribute to its lower propensity for causing extrapyramidal symptoms (EPS) and tardive schizophrenia, making it a promising alternative to classical antipsychotic therapies.
Used in Clinical Trials:
Perospirone is used as a subject in long-term clinical trials (lasting more than 6 months) to evaluate its efficacy in treating the positive, negative, and general symptoms of schizophrenia. These trials have demonstrated the effectiveness of perospirone at doses ranging from 12 mg to 96 mg t.i.d. compared to placebo.
Used in Anxiety Treatment:
Perospirone is used as an anxiolytic agent, as it has shown anxiolytic-like effects in animal models. This suggests that it may have potential applications in treating anxiety-related disorders in addition to its primary use in treating schizophrenia and other psychoses.
Brand Name:
Perospirone is marketed under the brand name Lullan.

Originator

Sumitomo Pharm. (Japan)

Check Digit Verification of cas no

The CAS Registry Mumber 150915-41-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,9,1 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 150915-41:
(8*1)+(7*5)+(6*0)+(5*9)+(4*1)+(3*5)+(2*4)+(1*1)=116
116 % 10 = 6
So 150915-41-6 is a valid CAS Registry Number.
InChI:InChI=1/C24H32N4O2S/c29-23-20-9-3-4-10-21(20)24(30)28(23)12-6-5-11-26-13-15-27(16-14-26)22-19-8-2-1-7-18(19)17-31-25-22/h1-2,7-8,20-21H,3-6,9-17H2/t20-,21+

150915-41-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product 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

1.2 Other means of identification

Product number -
Other names Lullan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:150915-41-6 SDS

150915-41-6Downstream Products

150915-41-6Relevant articles and documents

Combination treatment for anxiety, depression, obsessive compulsive disorder and psychosis

-

, (2008/06/13)

The present invention relates to a method of treating depression, obsessive compulsive disorder and psychosis in a mammal, including a human, by administering to the mammal an atypical antipsychotic in combination with an antidepressant agent with improvement in efficiency. It also relates to pharmaceutical compositions containing a pharmaceutically acceptable carrier, an atypical antipsychotic, and an SRI.

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