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SM 9018

pharmaceutical raw materials
SM 9018 structure

SM 9018 

structure
  • CAS No:

    129273-38-7

  • Formula:

    C23H30N4O2S.ClH

  • Chemical Name:

    SM 9018

  • Synonyms:

    1H-Isoindole-1,3(2H)-dione,2-[4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl]hexahydro-,hydrochloride (1:1),(3aR,7aS)-rel-;1H-Isoindole-1,3(2H)-dione,2-[4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl]hexahydro-,monohydrochloride,cis-;1H-Isoindole-1,3(2H)-dione,2-[4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl]hexahydro-,monohydrochloride,(3aR,7aS)-rel-;SM 9018;Perospirone hydrochloride

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

SM 9018 Basic Attributes

46304

462.185638

T884I76TMN

DTXSID9046449

Characteristics

84.99000

4.11650

95-970C

667.4ºC at 760 mmHg

357.4ºC

-20°C Freezer

Drug Information

Agents that control agitated psychotic behavior, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect. They are used in SCHIZOPHRENIA; senile dementia; transient psychosis following surgery; or MYOCARDIAL INFARCTION; etc. These drugs are often referred to as neuroleptics alluding to the tendency to produce neurological side effects, but not all antipsychotics are likely to produce such effects. Many of these drugs may also be effective against nausea, emesis, and pruritus. (See all compounds classified as Antipsychotic Agents.)

2-(4-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)butyl)hexahydro-1H-isoindole-1,3-(2H)-dione

Computed Properties

Molecular Weight:463.0
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:6
Exact Mass:462.1856251
Monoisotopic Mass:462.1856251
Topological Polar Surface Area:85
Heavy Atom Count:31
Complexity:615
Defined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

Drug Function and Efficacy

Perospirone is an atypical antipsychotic that works by affecting the dopamine metabolic pathway and blocking dopamine-2 and 5-HT2 receptors. Compared with haloperidol, perospirone has a stronger selectivity for the striatum, so it rarely causes extrapyramidal reactions. Non-clinical study results show that perospirone inhibits central stimulation or stereotyped behavior induced by methamphetamine or apomorphine in mice and rats, and inhibits conditioned avoidance reactions in rats by blocking dopamine-2 receptors; by blocking 5-HT2 receptors, it inhibits behavioral abnormalities such as forelimb spasms and increased body temperature in rats caused by tryptamine or PCA (parachlorophenylisopropylamine); in the rat conditioned affective disorder model, it can inhibit the onset of akinesia caused by psychological stress; perospirone has a low induction rate of stigma in rats and mice and bradykinesia in mice.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • Sichuan Tiandao Pharmaceutical Co., Ltd.

    China China
    Active
  • Hanrui Pharmaceutical (Jingmen) Co., Ltd.

    China China
    Active
  • Zhuhai Free Trade Zone Lizhu Synthetic Pharmaceutical Co., Ltd.

    China China
    Active

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