Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Diaryl and arylheteroaryl urea derivatives as modulators of the 5-ht2a serotonin receptor useful for the prophylaxis or treatment of progressive multifocal leukoencephalopathy

A leukoencephalopathy, alkyl technology, applied in the field of prevention or treatment of progressive multifocal leukoencephalopathy, can solve problems such as the absence of effective therapy

Inactive Publication Date: 2008-04-09
ARENA PHARMA
View PDF0 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Currently, no effective therapy exists

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Diaryl and arylheteroaryl urea derivatives as modulators of the 5-ht2a serotonin receptor useful for the prophylaxis or treatment of progressive multifocal leukoencephalopathy
  • Diaryl and arylheteroaryl urea derivatives as modulators of the 5-ht2a serotonin receptor useful for the prophylaxis or treatment of progressive multifocal leukoencephalopathy
  • Diaryl and arylheteroaryl urea derivatives as modulators of the 5-ht2a serotonin receptor useful for the prophylaxis or treatment of progressive multifocal leukoencephalopathy

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0586] The active content 125 I. The synthetic methods for incorporating the target molecule include:

[0587] A. Sandmeyer reaction and similar reactions-this procedure converts aryl or heteroaryl amines into diazonium salts, such as tetrafluoroborate and then Na 125 I convert it into 125 I labeled compound. The representative procedure was reported by Zhu, D.-G. and colleagues in J. Org, Chan. 2002, 67, 943-948.

[0588] B. Phenol ortho 125 Iodination reaction-this procedure allows incorporation at the ortho position of phenol 125 I, as reported by Collier, T.L. and colleagues in J. Labeled Compd Radiopharm 1999, 42, S264-S266. .

[0589] C. Take 125 I replace aryl and heteroaryl bromide-this method is usually a two-step method. The first step is, in the trialkyl tin halide or hexaalkyl ditin [for example (CH 3 ) 3 SnSn(CH 3 ) 3 ] In the presence of, for example, a reaction catalyzed by Pd [that is, Pd(Ph 3 P) 4 ] Or the aryl or heteroaryl bromide is converted to the correspondi...

example 1

[0596] Receptor cDNA

[0597] A. Constitutively activated 5-HT 2C Construction of receptor cDNA

[0598] 1. Endogenous human 5-HT 2C

[0599] Encoding endogenous human 5-HT 2C Receptor cDNA is made from human brain poly A + RNA was obtained by RT-PCR. The 5'and 3'primers are derived from the 5'and 3'untranslated regions and contain the following sequences:

[0600] 5'-GACCTCGAGGTTGCTTAAGACTGAAGCA-3' (SEQ.BD.NO.:1);

[0601] 5'-ATTTCTAGACATATGTAGCTTGTACCGT-3' (SEQ. ID. NO.: 2).

[0602] PCR is using TaqPlus TM Precision polymerase (Stratagene) or rTth TM Polymerase (Perkin Elmer) and the buffer system provided by the manufacturer, 0.25 μM each primer, and 0.2 mM four (4) nucleotides each were performed. The cycling conditions were 30 cycles, 1 minute at 94°C; 1 minute at 57°C and 2 minutes at 72°C. The 1.5 kb PCR fragment was digested with Xho I and XbaI and subcloned into the Sal I-Xba I site of pBluescript.

[0603] The cDNA thus obtained was fully sequenced and found to correspon...

example 2

[0647] Receptor expression

[0648] A.pCMV

[0649] For the purpose of producing related polypeptides in cells, a variety of expression vectors in this technology can be used. One suitable vector is pCMV used in certain embodiments. In accordance with the Budapest Treaty (Budapest Treaty) on the international recognition of the microbial preservation patent procedures, this vector was stored in the American Type Culture Collection (ATCC) (10801 University Blvd., October 13, 1998) Manassas, VA20110-2209USA). DNA is tested by ATCC and confirmed to be usable. ATCC awarded pCMV the following deposit number: ATCC#203351. See Figure 8 . Those skilled in the art will readily be apparent to other suitable expression vectors.

[0650] B. Transfection procedure

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
pore sizeaaaaaaaaaa
diameteraaaaaaaaaa
Login to View More

Abstract

The present invention relates to certain pyrazole derivatives of Formula (I) and pharmaceutical compositions thereof that modulate the activity of the 5-HT2A serotonin receptor. Compounds and pharmaceutical compositions thereof are directed to methods useful in the prophylaxis or treatment of progressive multifocal leukoencephalopathy.

Description

Technical field [0001] The present invention relates to certain diaryl and aryl heteroaryl urea derivatives of formula (I) and their pharmaceutical compositions, which regulate 5-HT 2A Serotonin receptor activity. The present invention is also directed to a method for the compound and its pharmaceutical composition to prevent or treat progressive multifocal leukoencephalopathy. Background technique [0002] G protein coupled receptor [0003] G protein-coupled receptors have a common structural motif. All these receptors have seven sequences containing 22 to 24 hydrophobic amino acids, which form seven alpha helices, each of which spans the membrane. The transmembrane helices are all connected by amino acid chains with larger loops between the fourth and fifth transmembrane helices on the outside of the cell membrane. However, another larger loop composed mainly of hydrophilic amino acids is connected to the fifth and sixth transmembrane helices inside the cell membrane. The carb...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): A61K31/415A61P25/28
CPCA61K31/415A61P25/00A61P25/28A61P31/18A61P35/00A61P37/00A61P37/02A61P9/00
Inventor 戴维·J·阿纳特布拉德利·蒂加登洪纳帕·贾亚库马尔李红梅索尼娅·斯特拉-普莱内特彼得·I·多莎
Owner ARENA PHARMA
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com