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Perlapine is an atypical neuroleptic that possesses the ability to block dopamine and serotonin (5-HT) receptors, specifically with Kis of 60, 30, and 30 nM for D2, D4, and 5-HT2A receptors, respectively. It also functions as an agonist for hM3Dq, a designer receptor exclusively activated by designer drugs (DREADD) that is derived from the human muscarinic acetylcholine M3 receptor. This unique characteristic allows perlapine to activate neuronal firing. Perlapine demonstrates a remarkable >10,000-fold selectivity for hM3Dq over hM3, making it a potentially effective compound in various applications.

1977-11-3

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1977-11-3 Usage

Uses

Used in Pharmaceutical Industry:
Perlapine is used as an antipsychotic agent for its ability to block dopamine and serotonin receptors, which can help in managing the symptoms of psychotic disorders. Its action on these receptors contributes to its antipsychotic activity, making it a valuable compound in the development of treatments for conditions such as schizophrenia and bipolar disorder.
Used in Neuroscience Research:
As a novel agonist of hM3Dq, perlapine is used in neuroscience research to study the effects of activating this designer receptor exclusively activated by designer drugs (DREADD). This application allows researchers to investigate the role of hM3Dq in neuronal firing and potentially uncover new insights into the functioning of the human muscarinic acetylcholine M3 receptor and related neurological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1977-11-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1977-11:
(6*1)+(5*9)+(4*7)+(3*7)+(2*1)+(1*1)=103
103 % 10 = 3
So 1977-11-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H21N3/c1-21-10-12-22(13-11-21)19-17-8-4-2-6-15(17)14-16-7-3-5-9-18(16)20-19/h2-9H,10-14H2,1H3

1977-11-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(4-methylpiperazin-1-yl)-11H-benzo[c][1]benzazepine

1.2 Other means of identification

Product number -
Other names 6-(4-Methyl-1-piperazinyl)morphanthridine

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:1977-11-3 SDS

1977-11-3Downstream Products

1977-11-3Relevant academic research and scientific papers

PESTICIDAL DIBENZO(HETERO)AZEPINE DERIVATIVES

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Page 75, (2010/02/07)

Use of compounds of formula (I): wherein X is S, O, S=O, SO2, NRa, or CRbRc;R1,R2 are halogen, OH, SH, NH2, CN, NO2, alkyl, alkoxy, alkylamino, dialkylamino, alkylthio

Morphanthridines: Part III - A New Synthesis of 6-(4-Methyl-1-piperazinyl)-morphanthridine

Sinha, Ashok Kumar,Nizamuddin, S.

, p. 165 (2007/10/02)

6-(4-Methyl-1-piperazinyl)morphanthridine (V) has been prepared by a new route involving Beckmann rearrangement of anthron-oxime (II) with PPA followed by treatment of the resultant 5,6-dihydro-6-oxomorphanthridine (III) with PCl5 and then with N-methylpiperazine.

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